Bioidentical Hormones 101
The Book, by Jeffrey Dach MD
Morning Rounds with Dr Steven G Economou
 Morning Rounds With Steven G. Economou MD by Jeffrey Dach MD (Link to this article) In 1977, I was a surgical intern at Rush Presbyterian St Luke's Hospital on the west side of Chicago. One floor of the hospital was devoted to caring for women with breast cancer, supervised by attending surgeon, Steven Economou MD. As a surgical intern, it was mandatory to attend a daily ritual called "morning rounds" to start off every work day.(see left image) Wearing long white coats and stethoscopes, we followed Dr. Economou around the floor, from patient room to patient room, reviewing charts, performing bedside examinations, and dispensing orders for diagnostic testing and treatment. Above Left image: courtesy of wikimedia commons, house staff on hospital rounds File:Bundesarchiv_Bild_183-1988-0809-316,_Rostock,_Klinik . A Game Called, "Stump the House Staff"  During
"Morning Rounds", Dr. Economou enjoyed playing a game called, "Stump
the House Staff". He would think up difficult questions and pose them
to us, as if they were were small darts thrown
to an imaginary target painted on the forehead of one of us
interns. As if it was yesterday, I can remember one such question he
asked me: "Dr. Dach, Does Estrogen cause breast cancer?" I was a cocky intern, just out of medical school, so I replied: "Of course estrogen causes breast cancer. Estrogen stimulates growth of breast tissue, and any growth stimulation will cause cancer." I assumed Dr Economou knew the correct answer and would provide it. To my surprise, he was silent, and offered no reply. He changed the subject and we continued on to the next patient room. Since that day in 1977, another 35 years of clinical research has elapsed, and medical science has embellished the answer in ways Dr Economou would have appreciated 35 years ago in 1977. Dr Steven G. Economou passed away at the age of 84 in 2007.(5) Above left image: Steven Economou MD, Surgeon Rush Medical Center Chicago, courtesy of the NIH and Raphael E Pollock MD , Annals of Surgical Oncology March 2008. Does Estrogen Cause Breast Cancer ? There are two parts to this answer: 1) It Depends on the Type of Estrogen Used. 2) It Depends on the Type of Progesterone Given Along With the Estrogen. Let's First look at the Effect of the Type of Estrogen Alone: Estradiol Alone - YES, this increases risk of breast by 30% French Cohort study. (5) Premarin Alone - NO, this decreases risk of breast cancer (WHI Second Arm)(1) Let's Look at the Added Progesterone : Progesterone Alone - No, this decreases risk of breast cancer.(35) Medroxyprogesterone (Provera) added- Yes, this increases risk of breast cancer (2) Norethinstrone added- another progestin- Yes, increased risk of breast cancer.(4,5) Estradiol-Alone The use of Estradiol-Alone IS associated with a 1.3 fold increase in breast cancer risk, as reported by Dr Fournier in the 2008 French Cohort study.(5) However, the combination of Estradiol and Progesterone (bioidentical) are not associated with increased breast cancer risk. This underscores the importance of the Estrogen/Progesterone combination as the safest program. For added safety, our Estrogen is a combination two ovarian estrogens, Estradiol (E2) and Estriol (E1) in a ratio of 20/80 called Bi-Est, invented and pioneered by Jonathan Wright MD. Estriol (E1) has been extensively studied and found preventive of breast cancer.(41-48) Premarin - No This Does NOT Cause Breast Cancer Premarin is estrogen from pregnant horses also called CEE, conjugated equine estrogen. The Premarin-Alone study, the 11 year follow up of the Women's Health Initiative was covered here.(1) Rather than causing breast cancer, Premarin (CEE) prevented it, finding a reduction in breast cancer for Post-Menopausal women using Premarin-Alone compared to placebo. To be exact, there was a 23% reduction in breast cancer in Premarin Users compared to placebo. (1) Premarin Plus MedroxyProgesterone (PremPro) - Yes, this Does Cause Breast Cancer The PremPro study was discussed here which was published in the October 2010 issue of JAMA. This study was the 11 year follow-up for the First Arm of the Women's Health Initiative. In this study, Prempro (Premarin plus Medroxyprogesterone) was given to post menopausal women. This PremPro study showed INCREASED breast cancer in the hormone treated group.(2) The hormone users had a 25 % increase in invasive breast cancer compared to placebo users. Breast cancer in the Prem-Pro users tended to more aggressive, with 78% more lymph node invasion, and greater mortality as well. (2) Premarin is OK, Premarin Plus Medroxyprogesterone is NOT OK So, here we see an obvious conclusion, that Premarin alone does not cause breast cancer and may even be preventive. Adding a synthetic chemically altered version of progesterone called a progestin (Medroxyprogesterone), DOES CAUSE breast cancer. Not only does Medroxyprogesterone cause breast cancer, these cancers tend to be more aggressive and are deadlier. (2) Progestins are Carcinogenic Medroxyprogesterone is Carcinogenic An explanation of the carcinogenic effect of progestins is contained in an article by Dr Horowitz in 2009 entitled " Progestins in Hormone Replacement Therapies Reactivate Cancer Stem Cells in Women With Preexisting Breast Cancers: A Hypothesis" (3) Noresthisterone is Carcinogenic Another Progestin known to be carcinogenic is Norethisterone which is widely used in Finland, and was the added Progestin in the HABITS study which showed (surprise) increased breast cancer in the hormone users.(4,5) Hormone Replacement for Breast Cancer Survivors - Will Hormone Replacement Cause Breast Cancer Recurrence ? For the past four decades, mainstream medicine has held the belief that hormone replacement is contra-indicated in the breast cancer survivor because of risk of causing cancer recurrence. Back in my internship days, Dr Economou frequently asked us this question: "If We Give Hormone Replacement to Breast Cancer Survivors, Will This Increase Rate of Breast Cancer Recurrence ?"Breast Cancer Prevention Program Firstly before we discuss giving hormones to the breast cancer survivor, let's give you information about our office program for breast cancer prevention which includes: Vitamin D Supplementation Vitamin D testing is important, and we optimize vitamin D to the upper end of the normal range for all patients. In a study reported in 2011 from Germany, lower vitamin D levels were inversely related to breast cancer recurrence and mortality. Higher Vitamin D levels were protective.(6) Iodine Supplementation Another test we use is the Spot Urinary Iodine level. We use Iodine supplementation with Iodoral. My previous article describes how iodine deficiency is a risk factor for breast cancer, and how Iodine supplementation prevents breast cancer, and can be used as adjuvant treatment. Here are the links: Iodine Prevents Breast Cancer Part One, Part two 2/16 Ratio - Urinary Estrogen Metabolite Testing- Meridian Valley Lab Meridian Valley is Dr. Jonathan Wright's lab which does urinary metabolite testing. He is the originator of Bi-Est formula commonly used in bioidentical hormone programs. Urinary metabolite testing is useful because some women will produce harmful estrogen metabolites which can increase the risk for breast cancer. The lab test is called the 2/16 ratio. Women with higher ratios have a 42% decrease in breast cancer (9,10). Nutritional supplements such as Indole-3-carbinol and Di-Indole-Methane are known to adjust the 2/16 ratio into a higher, more favorable balance.(11) Another question that frequently came up on rounds with Dr Steven G Economou is: Is Hormone Replacement Contra-Indicated for the Breast Cancer Survivor? Let's Ask William T. Creasman and Philip J. DiSaia  Both
Drs. William T. Creasman and Philip J. DiSaia are highly regarded
academic professors of Obstetrics and Gynecology, and authors of medical
textbooks of Gynecologic Oncology and Women's Health.
They advised in the 1980's that hormone replacement was
beneficial for the breast cancer survivor, and did not increase breast
cancer recurrence. Over the many decades of their careers, they have
written extensively about hormone replacement for the breast cancer
survivor. Above Left Image: Courtesy of William T. Creasman and Philip J. DiSaia Receiving Award for Excellence in OB Gyne Surgery. In a 2009 Letter to the Editor published in the journal, Oncology, Dr. Creasman writes the following: "numerous published articles have noted that recurrence rates in breast cancer survivors who chose to take HRT (Hormone Replacement Therapy) for symptom relief were very low."In 2005 Current Opinions in Oncology, Dr Creasman writes: "Several case-control and cohort studies have noted either no increased risk or actually less risk of recurrence in women taking estrogen after therapy after breast cancer. Although the general consensus is that such a recommendation is contraindicated, the data do not support this admonition." (7A,B,C)Dr Xydakis - Greece In agreement with Dr Creasman is Dr. Xydakis from Greece in the 2006 Annals of the New York Academy of Science says this (8): "No observational or retrospective study in breast cancer survivors (whether in pre- or postmenopausal women) has shown an increased risk of tumor recurrence or increased mortality associated with HRT use."(8)Eva Durna MD - Australia Also in agreement is Dr. Eva Durna from Australia.(12,13) She reported two observational studies. One in 2002 in which hormone replacement was given to post-menopausal breast cancer survivors, and one in 2004 in which hormone replacement was given to pre-menopausal (younger) breast cancer survivors. In both studies, Dr Eva Durna reports reduced mortality and reduced recurrence rates in the hormone users.(12,13) Dr Pelin Batur of the Cleveland Clinic Also in agreement is Dr. Pelin Batur of the Cleveland Clinic in a 2006 review of the medical literature published in Maturitas reviewing hormone replacement for breast cancer survivors.(39) Dr Pelin Batur identified seven studies which included a control group. Among 1,416 hormone replacement users, cancer reoccurrence was noted in 10.0%, while cancer recurrence was doubled (20%) for the non-hormone users. Cancer related mortality for hormone users was only 2.6% which was one third of the 7.8% cancer mortality in the non-hormone users.(39) Here is Dr. Batur's conclusion: "In our review, menopausal HT (hormone therapy) use in breast cancer survivors was not associated with increased cancer reoccurrence, cancer-related mortality or total mortality." (39)The Randomized Controlled Trial The way medical research works, first a number of observational studies are done which are reported in the medical literature, always with the caveat that they are only observational.(14,15,16) As Dr. Creasman reports, these observational studies are all in agreement that hormone replacement does not cause increased cancer recurrence in breast cancer survivors. Eventually the observational studies are either confirmed or refuted by randomized controlled trials (RCT's) which are considered more definitive evidence, the Gold Standard in medical research. Randomized Controlled Trials of HRT in Breast Cancer Survivors Two RCT studies were done, both from Sweden. The first is called HABITS (17,18,19), and the second is called the Stockholm study (20). Both studies gave hormone replacement to breast cancer survivors in a randomized trial compared to placebo. The HABITS study showed three times greater breast cancer recurrence in the hormone treated women, while the Stockholm study showed no increased recurrence. (17-20). How to Explain these Discrepant Findings? It Is The Tumor Grade ! Dr Chlebowski from Brown Medical School lamented in his 2005 systematic review of the medical literature that the findings of the randomized controlled trials were discrepant with the observational studies. (38) Dr. Chlebowski noted that the observation studies tended to enroll women with less aggressive breast cancers that were axillary lymph node negative.(38) This is common sense. If we as doctors are going to make the decision to either give or withhold HRT from the breast cancer survivor, it makes sense to withhold HRT from the more aggressive cases with axillary node involvement, and provide HRT for women with the less aggressive cancer cell types, and with no evidence of metastatic spread. It is the Progestin ! While it is clear that the horse estrogen-alone, Premarin-alone does not increase breast cancer risk(1), adding a synthetic progestin (MPA) increases breast cancer risk. For example, adding medroxyprogesterone resulted in a 1.48 fold increase, and Norethisterone a 2.11 increase in breast cancer. (5) Similarly, increased breast cancer risk was reported by the First Arm of the WHI using MedroxyProgesterone (2). HABITS- Norethisterone The ill-fated HABITS study used Norethisterone, a progestin that is known to be carcinogenic, associated with a 2-3 fold increase in breast cancer rates in Finland.(4,5) On the other hand, the more favorable Stockholm Study (20) had a larger number of women on Estrogen-Alone, as well the combination of estrogen and Medroxy-Progesterone. Medroxyprogesterone is carcinogenic, but less so than Norethisterone (4,5, 17) In both these Randomized Controlled Studies (RCT) of Breast Cancer Surivors given HRT, a Bioidentical Progesterone should have been used, as this is non-carcinogenic and actually preventive, as demonstrated in the French Cohort study reported by Plu-Bureau in 1999 in which users of topical progesterone had a significant reduction in breast cancer risk. (35) Previous studies in breast cancer survivors given a combination estrogen and progestin, Megace (21,22), also called Megestrol, showed protection from breast cancer recurrence, as this progestin has actually been useful in treatment of advanced breast cancer.(21,22) So in conclusion, the exact chemical composition of the added progestin plays a huge role in determining if the hormone replacement program will prevent or cause breast cancer. This is the point made by Dr Fournier in his 2008 French Cohort Study on the Unequal Risks For Breast Cancer Associated with Different Hormone Replacement Therapies. A quote from Dr Fournier 2008 report: "These findings suggest that the choice of the progestagen component in combined HRT is of importance regarding breast cancer risk; it could be preferable to use progesterone..."Another author, Dr Collins from Canada, independently agrees with Dr. Fournier. The added progestin determines breast cancer risk. Here is the quote from a 2005 article: "valid evidence from randomized controlled trials (RCTs) indicates that breast cancer risk is increased with estrogen-progestin use more than with estrogen alone."This is equally true for the breast cancer survivor seeking relief from menopausal symptoms. Of course, the safest and preferred hormone combination consists of replicating the endogenous ovarian hormones, Estradiol and Progesterone with topical delivery the preferred method. This, of course, is the concept of Bioidentical Hormones. BRCA Gene Positive Women and Hormone Replacement Studies on BRCA gene women are most revealing.(23-27) The BRCA gene is associated with 80% lifetime risk of breast cancer, and 20%-50% risk for ovarian cancer. BRCA Gene carrier women will frequently choose to have preventive oophorectomy (surgical removal of the ovaries) which induces surgical menopause. Therefore, it is not surprising that many of these women suffer with menopausal symptoms, and will seek relief with hormone replacement. A number of studies looking at hormone replacement in BRCA carrier women prior to or after oophorectomy show no increase in breast cancer risk from hormone replacement. A 2008 study by Dr. Eisen followed 472 post-menopausal women with BRCA mutation on hormone replacement for menopausal symptoms. In the BRCA gene women who took Estrogen-Alone, they found a 50% reduction in breast cancer rates.(23) Again, results for Estrogen-Alone were superior to the estrogen-progestin combination. Natural progesterone (bioidentical) is preferrable to the synthetic progestins. The experience with hormone replacement in BRCA gene carriers again suggests that Estrogen does not cause breast cancer, and is actually preventive. Rather, we know from current research that breast cancer is caused by oxidative damage to the DNA of breast cells. The BRCA gene mutation does exactly this, it causes malfunction of the anti-oxidant system. leading to oxidative damage to the DNA of the breast cell. Breast cancers in BRCA gene women tend to be triple negative , ie. estrogen, and progesterone receptor negative which are non-responsive to ovarian ablation. Ovarian Ablation as Treatment for Breast Cancer Breast cancer can occur in the younger pre-menopausal woman. Most commonly this is an indolent form of cancer called DCIS (ductal carcinoma in situ) which has a very good prognosis. However, another form of cancer (infiltrating ductal cancer) can be very aggressive in this age group with poor prognosis regardless of treatment. This variety tends to be estrogen receptor positive, and highly aggressive with a median survival of 26 months. (27-34) In this type of highly aggressive Estrogen-Receptor-Positive breast cancer in younger pre-menopausal women the mainstream medical treatment is ovarian ablation (either surgical or drug induced) to eliminate endogenous Estrogen.(28) In 2,100 pre-menopausal estrogen receptor positive breast cancer patients, ovarian ablation improved 15 year survival from 46% to 52%. (29) This is a six per cent absolute benefit, which is quite disappointing.(29) This again underscores the aggressive nature of this variety of breast cancer, and the futility of mainstream treatment. Obviously, in this scenario, hormone replacement would be contra-indicated. For women over the age of 50, ovarian ablation was of no benefit regardless of tumor receptor status.(29) So, patient age, tumor grade and hormone receptor status, and disease free years since diagnosis and treatment are important considerations when considering whether or not to offer hormone replacement program for the breast cancer survivor. (27-34) Family History of Breast Cancer The benefits of hormone replacement extend to women with a family history of breast cancer. A 1997 study in Iowa followed 41,800 women for 8 years. Those women using hormone replacement who had a history of breast cancer in a family member still had a 50% reduction in over all mortality compared to non-users.(36) There was a slight increase in breast cancer in the hormone users in this observational study. However this was not statistically significant. (36) Opposing Opinions - Confusing Progestins with Progesterone To be fair, a number mainstream authors oppose Dr. Creasman's opinion such as Dr Labriola in a 2009 rebuttal letter (40) Again, the opposing views are usually based on the confusion of chemically altered progestins which are known to be carcinogenic, with the ovarian hormone, progesterone. Progestins are not progesterone. They have an entirely different chemical structure and different biological activity profile. As you read through the medical literature you will find a common mistake. Many of the reference articles on this topic use mistaken terminology, referring to a "progestin" hormone as "progesterone" which it is not.(7a)(23) For example Dr Andrea Eisen's BRCA gene article says that the first arm of the WHI used a combination pill consisting of Estrogen and Progesterone which increased breast cancer risk. (23) This is entirely incorrect, as the WHI study actually used Premarin and Provera (medroxyprogesterone), a progestin. Progestin use is associated with increased breast cancer, while Progesterone is not. This mistake permeates the women's hormone literature explaining the many discrepancies in findings and opinions. So when you see the word progesterone in a medical report, you have to ask yourself, does the author really mean "progesterone", or was in fact a "progestin" given to these women? Randomized Trials With Bioidentical Estradiol and Progesterone Urgently Needed Unfortunately, as yet, after all these years, there are still no randomized trials (RCT) of postmenopausal hormone replacement with commonly used bioidentical hormone preparations such as topical Bi-Est (80% estriol and 20% estradiol) and topical Progesterone. We urgently need RCT studies of bioidentical hormone therapies in breast cancer survivors as well. This article is part one of a series, click here for Part Two. Articles With Related Interest: Iodine Prevents Breast Cancer Part One Iodine Prevents Breast Cancer Part Two The Safety of Bio-Identical Hormones The Importance of BioIdentical Hormones Bioidentical Hormones Prevent Arthritis Bioidentical Hormone Estrogen Prevents Heart Disease Morning Rounds With Steven Economou MD Waking Up from the Synthetic Hormone Nightmare HRT Does Not Cause Breast Cancer Bioidentical Hormones Beneficial After Hysterectomy Jeffrey Dach MD 7450 Griffin Road, Suite 190 Davie, Fl 33314 954-792-4663 www.jeffreydach.com www.drdach.com www.naturalmedicine101.com www.bioidenticalhormones101.com www.truemedmd.com Links and References ... (0) http://articles.chicagotribune.com/2007-04-28/news/0704271171_1_surgery-department-rush-university-medical-center-presbyterian-hospital Steven G. Economou: 1922 - 2007 Surgeon, writer, doodler April 28, 2007|By Trevor Jensen, Tribune staff reporter Steven G. Economou was adept with both scalpel and pen, chairing the surgery department at what is now Rush University Medical Center and writing dozens of medical articles and doodling abstract figures that illustrated his self-published books. Dr. Economou, 84, died Saturday, April 7, at Rush North Shore Medical Center in Skokie of complications from illnesses including Parkinson's disease, said his wife, Kathryn, who goes by the name "Kitty." 1) jama.ama-assn.org/content/305/13/1305.abstract JAMA. 2011;305(13):1305-1314. Health Outcomes After Stopping Conjugated Equine Estrogens Among Postmenopausal Women With Prior Hysterectomy A Randomized Controlled Trial Andrea Z. LaCroix, PhD; Rowan T. Chlebowski, MD, PhD;et al for the WHI Investigators Over the entire follow-up, lower breast cancer incidence in the CEE group persisted and was 0.27% compared with 0.35% in the placebo group (HR, 0.77; 95% CI, 0.62-0.95). (2) http://jama.ama-assn.org/cgi/content/abstract/304/15/1684 Estrogen Plus Progestin and Breast Cancer
Incidence and Mortality in Postmenopausal Women - Rowan T. Chlebowski,
MD, PhD et al.
for the WHI Investigators Following the initial report of results from the WHI trial,1 a substantial decrease in breast cancer incidence occurred in the United States, which was attributed24-25 to the marked decrease in postmenopausal hormone therapy use that occurred after publication of the trial results.26 The adverse influence of estrogen plus progestin on breast cancer mortality suggests that a future reduction in breast cancer mortality in the United States may be anticipated as well. In intention-to-treat analysis, estrogen plus progestin compared with placebo increased the incidence of invasive breast cancer (385 cases [0.42% per year] vs 293 cases [0.34% per year], respectively; HR, 1.25; 95% confidence interval [CI], 1.07-1.46; P = .004). A significantly larger fraction of breast cancers presented with positive lymph nodes in the combined hormone therapy group compared with the placebo group (81 [23.7%] vs 43 [16.2%], respectively; HR, 1.78; 95% CI, 1.23-2.58; P = .03). In conclusion, use of estrogen plus progestin increases the incidence of breast cancer, and the cancers are more commonly node-positive. Mortality data analyses suggest that breast cancer mortality may also be increased. 2009 Progestins Are Carcinogenic-reactivate cancer stem cells (3) jcem.endojournals.org/content/93/9/3295.full www.ncbi.nlm.nih.gov/pmc/articles/PMC2567860/ Progestins in Hormone Replacement Therapies Reactivate Cancer Stem Cells in Women With Preexisting Breast Cancers: A Hypothesis Obstetrical & Gynecological Survey: August 2009 V64,8, pp 525-526 by Horwitz, Kathryn B.; Sartorius, Carol A. An increased risk of invasive, estrogen receptor-positive (ER+) breast cancer in the combined estrogen plus progestin arm of the Women's Health Initiative menopausal hormone replacement therapy (HRT) trial was in large part responsible for stopping the study prematurely in 2002. Subsequent studies offered several possibilities to explain how addition of progestins to estrogens increases the risk of breast cancer. The authors of this report offer a hypothesis for the increased risk based on their research and that of other investigators. A rare small tumorigenic subpopulation of estrogen receptor-negative, progesterone receptor-negative cancer stem cells is present in experimental ER+, progesterone receptor-positive human breast cancers. Progestins but not estrogens act on the ER+, progesterone receptor-positive differentiated cells (especially in small nascent tumor colonies) to reactivate and revert to the more primitive estrogen receptor-negative, progesterone receptor-negative stem cells without requiring proliferation. The authors propose that a reservoir of occult, undetected, preinvasive breast cancer or dormant breast cancer stem cells is present before the start of estrogen plus progestin therapy in some women. Autopsy data of women over 40 years of age who did not have known breast cancer during life showed that the median prevalence of invasive breast cancer at death was 1.3% (range: 0%-1.8%), and the median prevalence of ductal carcinoma in situ was 8.9% (range: 0%-14%). Estrogens are not involved in the activation process, but once receptors are reacquired, they can act through their mitogenic properties to expand the tumor cell population. The authors believe that improved screening methods are needed to detect occult, possibly dormant, breast cancers before initiation of hormone replacement therapy. If the hypothesis is correct, women with such preexisting malignancies should be excluded from regimens containing systemic progestins. 2010 - Finland - Norethisterone known to double breast cancer rate (4) http://onlinelibrary.wiley.com/doi/10.1002/ijc.24996/full Do the dose or route of administration of norethisterone acetate as a part of hormone therapy play a role in risk of breast cancer: National-wide case-control study from Finland by Heli Lyytinen1, Tadeusz Dyba2, Eero Pukkala2,3, Olavi Ylikorkal International Journal of Cancer Volume 127, Issue 1, pages 185–189, 1 July 2010 It is established that the use of postmenopausal estrogen–progestagen therapy (EPT) is associated with a higher risk elevation for breast cancer than is the sole use of estrogen.1–3 This may imply that progestagen, alone or in combination with estrogen, is more crucial for the possible initiation and/or growth of breast cancer than is estrogen. Modern recommendations advocate the use of the lowest effective doses, and then the main focus has been placed on the dose of estrogen.4–9 Indeed, no data exist on the daily dose-dependence between progestagen and the risk for breast cancer, although the higher risks associated with continuous EPT rather than sequential EPT use may hint at such a dependence.1, 10 In Finland, the most common progestagen as a part of EPT is norethisterone acetate (NETA), which can be given both orally and transdermally.3 The use of a “low” dose NETA-regimen was associated with an increased risk for breast cancer already in 3 years of use (1.94; 1.39–2.70) 2008 - Norethisterone Doubles Breast Cancer- French Cohort Study (5) http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2211383/ Unequal risks for breast cancer associated with different hormone replacement therapies: results from the E3N cohort study by Agnès Fournier,1 Franco Berrino,2 and Françoise Clavel-Chapelon1, Breast Cancer Res Treat. 2008 January; 107(1): 103–111. ----------------- Vitamin D prevents >55 improves overall and disease free survival after BRCA. Germany 6) http://www.biomedcentral.com/content/pdf/bcr2920.pdf Breast Cancer Res. 2011 Jul 26;13(4):R74. Serum 25-hydroxyvitamin D and postmenopausal breast cancer survival: a prospective patient cohort study. Vrieling A, Hein R, Abbas S, Schneeweiss A, Flesch-Janys D, Chang-Claude J. Division of Cancer Epidemiology, German Cancer Research Center, Im Neuenheimer Feld 581, 69120 Heidelberg, Germany. the aim of our study was to assess the effect of post-diagnostic serum 25-hydroxyvitamin D [25(OH)D] concentrations on overall survival and distant disease-free survival. METHODS: We conducted a prospective cohort study in Germany including 1,295 incident postmenopausal breast cancer patients aged 50-74 years. Patients were diagnosed between 2002 and 2005 and median follow-up was 5.8 years. RESULTS: Lower concentrations of 25(OH)D were linearly associated with higher risk of death (hazard ratio (HR) = 1.08 per 10 nmol/L decrement; 95% confidence interval (CI), 1.00 to 1.17) and significantly higher risk of distant recurrence (HR = 1.14 per 10 nmol/L decrement; 95%CI, 1.05 to 1.24). Compared with the highest tertile (≥ 55 nmol/L), patients within the lowest tertile (< 35 nmol/L) of 25(OH)D had a HR for overall survival of 1.55 (95%CI, 1.00 to 2.39) and a HR for distant disease-free survival of 2.09 (95%CI, 1.29 to 3.41). CONCLUSIONS:In conclusion, lower serum 25(OH)D concentrations may be associated with poorer overall survival and distant disease-free survival in postmenopausal breast cancer patients. --------------------------------------------------------------- William Creasman MD Nov 2009 Letter to the Editor 7) http://www.cancernetwork.com/breast-cancer/content/article/10165/1486356 Hormone Replacement and Breast Cancer Risk: Reconsidering the Data by By William T. Creasman, MD Department of Obstetrics and Gynecology Medical University of South Carolina Charleston, South Carolina and Philip J. DiSaia, MD Department of Obstetrics and Gynecology University of California, Irvine Irvine, California | ONCOLOGY. Vol. 23 No. 12 , November 12, 2009 In their recent commentary (ONCOLOGY 23:639-641, 2009), Labriola and colleagues reviewed the data on “natural” hormone replacement and breast cancer risk. The “natural” agents were bioidentical and phytoestrogen supplements to manage vasomotor symptoms in breast cancer patients. The rationale for the alternative was the fact that in one large study, the women who took conventional hormone replacement therapy (HRT) preparations had a higher risk for breast cancer, and therefore, similar preparations could not be used in breast cancer survivors with vasomotor symptoms. The authors justified that statement by citing the 2002 Women’s Health Initiative (WHI) study.[1] This study compared estrogen plus progestin with a placebo. Another prospective randomized group mentioned by the authors received estrogen alone compared to a placebo, but this study was not referenced. We remain amazed at the literature that incriminates estrogen/progestin and estrogen alone, quoting the 2002 WHI article for estrogen/progestin even though there have been over 100 articles from the WHI since then, in which a significant amount of the 2002 data have been temporized or shown not to support the conclusions of the 2002 publication. Many articles have been written severely criticizing the methodology of the WHI study, including eligibility, surveillance, presentation of nonadjudicated data, and certainly the age of the participants, to name a few. We are not writing to reiterate those faults, but to suggest that recent WHI data do not note an increase in breast cancer risk. (MORE: ‘Natural’ Hormone Replacement and Breast Cancer Risk: Evidence for Safety and Efficacy) Evolving WHI Data The 2002 article stated that the hazard ratio (HR) for estrogen plus progestin was 1.26 (95% confidence interval [CI] = 1.0–1.59), which is not statistically significant but was the reason for stopping the study. In a 2003 article, the HR was 1.24 (95% CI = 1.01–1.54), now barely significant as the number of breast cancers had increased since the 2002 publication.[2] In the 2006 publication on estrogen plus progestin, the adjusted HR was 1.20 (95% CI = 0.94–1.53).[3] Although the WHI investigators may have been under significant pressure to publish data from the study, we suggest that it may have been reported prematurely, and the bulk of the patients were elderly women upon enrollment. More women who were 50 to 59 years of age, or less than 10 years from menopause should have been enrolled. In truth, how many 70-year-old women are placed on HRT for the first time? In the 50- to 59-year-old age group, not only was there no increased risk, but the HR was actually less than 1.[4] In their rather detailed article on younger women with cardiovascular disease, the investigators commented that women less than 10 years since menopause had an HR of 1.19 (95% CI = 0.84–1.70) for breast cancer.[4] This is certainly not statistically significant. In 2004, the data on estrogen alone was presented for the first time (a prospective randomized study of about 10,000 women compared to over 16,000 women in the estrogen/progestin study). The HR for breast cancer was 0.77 (95% CI = 0.59–1.01).[5] In the 50- to 59-year-olds, the HR was 0.72 (95% CI = 0.43–1.21). In 2006, a 7.1-year follow-up of estrogen and breast cancer risk was published. If a woman had no prior replacement therapy history, her HR was 0.76 (95% CI = 0.58–0.99), her risk for ductal cancer was 0.71 (95% CI = 0.52–0.99), and if she was adherent in regard to taking her medication, the HR was 0.67 (95% CI = 0.47–0.97).[6] Therefore, we question the assumption that estrogen/progestin and estrogen alone increase the risk of breast cancer using the studies that the commentary referenced. Historical Perspective That being the case, why is traditional HRT contraindicated in women who have had breast cancer? From a historical perspective, for many years estrogen was used as primary treatment for postmenopausal women with recurrent or metastatic breast cancer. In the 1970s and early 1980s, several prospective randomized studies compared estrogen with tamoxifen(Drug information on tamoxifen) in such women. The results were similar.[7] Since alternatives, as noted in the commentary, are not very effective, numerous published articles have noted that recurrence rates in breast cancer survivors who chose to take HRT for symptom relief were very low. Yes, these were retrospective studies with built-in bias. One bias may come from the woman herself, as she chooses to take the hormones. Several case control and cohort studies have compared HRT with such controls, and in over 1,200 cases and 3,800 controls, there was twice as many recurrences in the controls as in those on hormones.[6] Two prospective randomized studies have compared hormones with controls. Both of these studies originated in Sweden. In the HABITS study, 442 women were randomized to receive hormones or no hormones for 2 years. The initial report in 2004 noted an HR of 3.3 (95% CI = 1.5–7.4), and the study was stopped.[9] A 4-year follow-up noted an adjusted HR of 2.2 (95% CI = 1.0–5.0).[10] The other study (the Stockholm trial) randomized 359 breast cancer women to 5 years of hormones or no hormones. Data reported in 2008 noted an HR of 0.8 (95% CI = 0.35–1.9).[11] The investigators found no difference in breast cancer deaths between the hormone and no-hormone groups in either study. Importance of Options These data on HRT in breast cancer patients are not well disseminated. In many instances, women are told that HRT is absolutely contraindicated, yet we are unaware of any clinical data to substantiate that statement. In view of the present data, we feel it is important for women to know there are choices, and current data would suggest that there is no increased risk of recurrence with HRT. Once women are given data and they have made a decision, we as health-care professionals should support them and not criticize that decision. Why is HRT contraindicated in a 50-year-old newly menopausal breast cancer survivor who was successfully treated for her cancer at 40 years of age? Hasn’t she been getting endogenous estrogen for the last 10 years? This question and others make these authors question the tenet that postmenopausal estrogen therapy is always contraindicated in a woman who has had breast cancer. 2005 Creaseman Very good 2005 Creaseman 7a) www.ncbi.nlm.nih.gov/pubmed/16093802 Curr Opin Oncol. 2005 Sep;17(5):493-9. Hormone replacement therapy after cancers. Creasman WT. Department of Obstetrics and Gynecology, Medical University of South Carolina, 96 Jonathan Lucas Street, PO Box 250619, Charleston, SC 29425, USA. creasman@musc.edu The role of female hormones in estrogen-dependent cancers has been debated for years. This is particularly true of breast cancer. Retrospective, case, and cohort control studies usually have suggested no influence. The Women's Health Initiative study in 2002, a prospective double-blind study, noted an increased risk of breast cancer if estrogen plus progesterone was given. (Dr Dach note: the above should read Premarin and the progestin, Provera, not estrogen and progesterone) In the estrogen-only arm of that study, a decreased (not significant) risk of breast cancer was noted. With this controversy, can estrogen be given safely to a woman who has been treated for breast cancer? The relation between endometrial cancer and unopposed estrogen is well established. With clear-cut evidence of this relation, is there evidence to suggest a role for replacement therapy in women who have been treated for endometrial cancer? RECENT FINDINGS: Several case-control and cohort studies have noted either no increased risk or actually less risk of recurrence in women taking estrogen after therapy after breast cancer. Although the general consensus is that such a recommendation is contraindicated, the data do not support this admonition. The current data suggest that replacement therapy can be given to the woman who has been treated for endometrial cancer. SUMMARY:"There seems to be little if any risk in giving hormone replacement therapy to women who have had breast or endometrial cancer. There are no data to suggest that hormone replacement therapy is contraindicated in women who have been treated for cervical or ovarian cancer." Ever since Professor William T. Creasman suggested the use of hormone replacement therapy in breast cancer survivors in the early 1980s, interest in this field has been guarded but present. Prescribing HRT to breast cancer survivors was initially thought of as being outrageous. Yet even then with experience in HRT spanning a good three decades, and with the breast cancer epidemic, so confidently predicted, then as it is now never actually materializing, doctors working in the field had started to question the conventional wisdom. The debate on whether to treat breast cancer survivors with HRT has been revisited from time to time as there has been a powerful demand for a solution for such symptomatic women. 7b) win.menopausaitaliana.it/hrt%20dopo%20cancro%20creasman%202005.pdf www.ncbi.nlm.nih.gov/pubmed/16093802 Hormone replacement therapy after cancers by William T. Creasman Curr Opin Oncol. 2005 Sep;17(5):493-9. Hormone replacement therapy after cancers. Creasman WT. Department of Obstetrics and Gynecology, Medical University of South Carolina, 96 Jonathan Lucas Street, PO Box 250619, Charleston, SC 29425, USA. The role of female hormones in estrogen-dependent cancers has been debated for years. This is particularly true of breast cancer. Retrospective, case, and cohort control studies usually have suggested no influence. The Women's Health Initiative study in 2002, a prospective double-blind study, noted an increased risk of breast cancer if estrogen plus progesterone was given. In the estrogen-only arm of that study, a decreased (not significant) risk of breast cancer was noted. With this controversy, can estrogen be given safely to a woman who has been treated for breast cancer? The relation between endometrial cancer and unopposed estrogen is well established. With clear-cut evidence of this relation, is there evidence to suggest a role for replacement therapy in women who have been treated for endometrial cancer? RECENT FINDINGS:Several case-control and cohort studies have noted either no increased risk or actually less risk of recurrence in women taking estrogen after therapy after breast cancer. Although the general consensus is that such a recommendation is contraindicated, the data do not support this admonition. The current data suggest that replacement therapy can be given to the woman who has been treated for endometrial cancer. SUMMARY:There seems to be little if any risk in giving hormone replacement therapy to women who have had breast or endometrial cancer. There are no data to suggest that hormone replacement therapy is contraindicated in women who have been treated for cervical or ovarian cancer 8) http://www.ncbi.nlm.nih.gov/pubmed/17308160 Ann N Y Acad Sci. 2006 Dec;1092:349-60. Hormone replacement therapy in breast cancer survivors. Xydakis AM, Sakkas EG, Mastorakos G. Second Department of Obstetrics and Gynicology, Aretaieion Hospital, Medical School, University of Athens, Athens, Greece. It is well known that women with breast cancer who undergo therapies beyond the surgical intervention (adjuvant chemotherapy, hormone therapy, or both) often suffer from the lack of estrogen, manifesting as climacteric symptoms in either treated premenopausal or postmenopausal women. Although HRT (hormone replacement therapy) is traditionally viewed as a contraindication in women with a history of breast cancer, more women are willing to receive HRT for symptom relief. "No observational or retrospective study in breast cancer survivors (whether in pre- or postmenopausal women) has shown an increased risk of tumor recurrence or increased mortality associated with HRT use." Nevertheless, because these studies are retrospective and different in terms of lymph node status, estrogen receptor (ER) status, and type of HRT used, firm conclusions on potential HRT use cannot be safely drawn. The few prospective studies appear controversial possibly due to differences in the studies' design. A potential scheme for possible HRT use in selected breast cancer survivors with severe climacteric symptoms is suggested. The duration of HRT use is debatable because there is insufficient evidence at present. However, the available data suggest that 3-year and possibly 5-year HRT use may be safe. In summary, while HRT cannot currently be recommended as first-line therapy, it may still be of benefit in the management of selected early stage breast cancer survivors with refractory climacteric symptoms after a well-informed decision and an individualized risk benefit discussion. 2/16 alpha-hydroxyestrone Ratio 9) http://www.ncbi.nlm.nih.gov/pubmed/9663330 Ann Acad Med Singapore. 1998 Mar;27(2):294-9. Urinary 2/16 alpha-hydroxyestrone ratio: correlation with serum insulin-like growth factor binding protein-3 and a potential biomarker of breast cancer risk. Ho GH, Luo XW, Ji CY, Foo SC, Ng EH. Department of Surgery, Singapore General Hospital, Singapore. Metabolism of estradiol occurs via two mutually exclusive hydroxylative pathways, yielding metabolites of divergent biological properties. 2-hydroxyestrone (2OHE1) is anti-estrogenic while 16 alpha-hydroxyestrone (16 alpha OHE1) is a potent estrogen. The ratio of 2OHE1 to 16 alpha OHE1 (2/16 alpha-OHE1 ratio) represents the net in vivo estrogenic activity. In this study, we sought to determine if the urinary 2/16 alpha-OHE1 ratio could be a predictor of breast cancer risk and the factors which influence this ratio. Variables analysed included age at diagnosis, menopausal status, parity, use of oral contraceptives, body mass index, serum levels of insulin-like growth factor-I (IGF-I), IGF binding proteins (BPs) and the presence of breast cancer. Serum and urine were collected from 65 breast cancer patients and 36 controls after an overnight fast. Urinary estrogen metabolites were measured by enzyme immunoassays while serum levels of IGF-I, BP-1 and BP-3 were determined by immunoradiometric assays. 2OHE1 levels and 2/16 alpha-OHE1 ratios were significantly lower (P < 0.05) while 16 alpha OHE1 levels were higher (P < 0.01) in cancer patients. Multiple linear regression analysis showed that levels of urinary metabolites were influenced by parity and breast carcinoma. 2/16 alpha-OHE1 ratio correlated positively with serum BP-3 level (P = 0.03). By multiple logistic regression, 2/16 alpha-OHE1 ratio was the most significant factor predictive of breast cancer. The odds ratio for women with higher 2/16 alpha-OHE1 ratios was 0.10 (0.03-0.38, 95% confidence interval). In conclusion, the profile of urinary estradiol metabolites was distinctly altered in breast cancer patients. In addition, BP-3 may be a potential mechanism by which estradiol metabolites influence breast cancer progression. As 16 alpha OHE1 has been shown to initiate neoplastic transformation of mammary epithelial cells, the 2/16 alpha-OHE1 ratio may serve as a biomarker of increased risk of breast cancer. 10) http://www.ncbi.nlm.nih.gov/pubmed/11055622 Epidemiology. 2000 Nov;11(6):635-40. Estrogen metabolism and risk of breast cancer: a prospective study of the 2:16alpha-hydroxyestrone ratio in premenopausal and postmenopausal women. Muti P, Bradlow HL, Micheli A, Krogh V, Freudenheim JL, Schünemann HJ, Stanulla M, Yang J, Sepkovic DW, Trevisan M, Berrino F. Department of Social and Preventive Medicine, University at Buffalo, State University of New York at Buffalo, 14226, USA. Experimental and clinical evidence suggests that 16alpha-hydroxylated estrogen metabolites, biologically strong estrogens, are associated with breast cancer risk, while 2-hydroxylated metabolites, with lower estrogenic activity, are weakly related to this disease. This study analyzes the association of breast cancer risk with estrogen metabolism, expressed as the ratio of 2-hydroxyestrone to 16alpha-hydroxyestrone, in a prospective nested case-control study. Between 1987 and 1992, 10,786 women (ages 35-69 years) were recruited to a prospective study on breast cancer in Italy, the "Hormones and Diet in the Etiology of Breast Cancer" (ORDET) study. Women with a history of cancer and women on hormone therapy were excluded at baseline. At recruitment, overnight urine was collected from all participants and stored at -80 degrees C. After an average of 5.5 years of follow-up, 144 breast cancer cases and four matched controls for each case were identified among the participants of the cohort. Among premenopausal women, a higher ratio of 2-hydroxyestrone to 16alpha-hydroxyestrone at baseline was associated with a reduced risk of breast cancer: women in the highest quintile of the ratio had an adjusted odds ratio (OR) for breast cancer of 0.58 [95% confidence interval (CI) = 0.25-1.34]. The corresponding adjusted OR in postmenopausal women was 1.29 (95% CI = 0.53-3.10). Results of this prospective study support the hypothesis that the estrogen metabolism pathway favoring 2-hydroxylation over 16alpha-hydroxylation is associated with a reduced risk of invasive breast cancer risk in premenopausal women. 11) http://www.altmedrev.com/publications/7/2/112.pdf Altern Med Rev. 2002 Apr;7(2):112-29. Estrogen metabolism and the diet-cancer connection: rationale for assessing the ratio of urinary hydroxylated estrogen metabolites. by Lord RS, Bongiovanni B, Bralley JA. MetaMetrix Clinical Laboratory, 4855 Peachtree Industrial Boulevard, Suite 201, Norcross, GA, 30092, USA. Estrogens are known for their proliferative effects on estrogen-sensitive tissues resulting in tumorigenesis. Results of experiments in multiple laboratories over the last 20 years have shown that a large part of the cancer-inducing effect of estrogen involves the formation of agonistic metabolites of estrogen, especially 16-alpha-hydroxyestrone. Other metabolites, such as 2-hydroxyestrone and 2-hydroxyestradiol, offer protection against the estrogen-agonist effects of 16-alpha-hydroxyestrone. An ELISA method for measuring 2- and 16-alpha-hydroxylated estrogen (OHE) metabolites in urine is available and the ratio of urinary 2-OHE/16-alpha-OHE (2/16-alpha ratio) is a useful biomarker for estrogen-related cancer risk. The CYP1A1 enzyme that catalyzes 2-hydroxyestrone (2-OHE1) formation is inducible by dietary modification and supplementation with the active components of cruciferous vegetables, indole-3-carbinol (I-3-C), or diindolylmethane (DIM). Other dietary components, especially omega-3 polyunsaturated fatty acids and lignans in foods like flax seed, also exert favorable effects on estrogen metabolism. Thus, there appear to be effective dietary means for reducing cancer risk by improving estrogen metabolism. This review presents the accumulated evidence to help clinicians evaluate the merit of using tests that measure estrogen metabolites and using interventions to modify estrogen metabolism. 2004- Durna-Australia- Premenopausal BR CA -observational study 12) www.ncbi.nlm.nih.gov/pubmed/15669553 Climacteric. 2004 Sep;7(3):284-91. Breast cancer in premenopausal women: recurrence and survival rates and relationship to hormone replacement therapy. by Durna EM, Heller GZ, Leader LR, Sjoblom P, Eden JA, Wren BG. Source School of Women's and Children's Health, University of New South Wales, Sydney, Australia. To determine any association between hormonal replacement therapy (HRT) usage and breast cancer recurrence and survival rates in women who were premenopausal at the time of diagnosis of breast cancer. METHODS: The study group comprised 524 women who were diagnosed with breast cancer when they were premenopausal. Of these, 277 women reached menopause before recurrence of the disease, being lost to follow-up, or reaching the end of the study. In this group, 119 women took HRT to control menopausal symptoms. The majority took combined continuous estrogen-progestin treatment. Times from diagnosis to cancer recurrence or new breast cancer, to death from all causes, and to death from primary tumor were compared between HRT users and non-users. RESULTS:Women who used HRT after their menopause had an adjusted relative risk of recurrence or new breast cancer of 0.75 (95% confidence interval (CI), 0.29-1.95) compared to that of non-users. The relative risk of death from all causes was 0.36 (95% CI, 0.11-1.16) and that of death from primary tumor was 0.24 (95% CI, 0.05-1.14). CONCLUSION: HRT use in women who were premenopausal at the diagnosis of primary invasive breast cancer is not associated with worse outcomes in terms of breast cancer recurrence or mortality. 2002 -Observational Study Australia Dr - Durna 13) www.ncbi.nlm.nih.gov/pubmed/12358575 Med J Aust. 2002 Oct 7;177(7):347-51. Hormone replacement therapy after a diagnosis of breast cancer: cancer recurrence and mortality. by Durna EM, Wren BG, Heller GZ, Leader LR, Sjoblom P, Eden JA. Source School of Women's and Children's Health, University of New South Wales, Sydney, NSW, Australia. To determine whether hormone replacement therapy (HRT) after treatment for breast cancer is associated with increased risk of recurrence and mortality. DESIGN: Retrospective observational study. PARTICIPANTS AND SETTING: Postmenopausal women diagnosed with breast cancer and treated by five Sydney doctors between 1964 and 1999. OUTCOME MEASURES: Times from diagnosis to cancer recurrence or new breast cancer, to death from all causes and to death from primary tumour were compared between women who used HRT for menopausal symptoms after diagnosis and those who did not. Relative risks (RRs) were determined from Cox regression analyses, adjusted for patient and tumour characteristics. RESULTS: 1122 women were followed up for 0-36 years (median, 6.08 years); 154 were lost to follow-up. 286 women used HRT for menopausal symptoms for up to 26 years (median, 1.75 years). Compared with non-users, HRT users had reduced risk of cancer recurrence (adjusted relative risk [RR], 0.62; 95% CI, 0.43-0.87), all-cause mortality (RR, 0.34; 95% CI, 0.19-0.59) and death from primary tumour (RR, 0.40; 95% CI, 0.22-0.72). Continuous combined HRT was associated with a reduced risk of death from primary tumour (RR, 0.32; 95% CI, 0.12-0.88) and all-cause mortality (RR, 0.27; 95% CI, 0.10-0.73). CONCLUSION: HRT use for menopausal symptoms by women treated for primary invasive breast cancer is not associated with an increased risk of breast cancer recurrence or shortened life expectancy. 2002 WILLIAM CREASMAN, MD 14) www.jfponline.com/pages.asp?aid=2920 Journal of Family Practice June 2002 · Vol. 14, No. 6 Weighing HRT use after breast cancer HRT has long been contraindicated in women who have—or have had—breast cancer. Here, the author examines the effects estrogen has on the breast and reviews several studies that suggest HRT actually may be of benefit to these women. WILLIAM CREASMAN, MD - Dr. Creasman is the J. Marion Sims Professor of OBG at the Medical University of South Carolina in Charleston. 15) www.obgmanagement.com/pdf/1406/1406OBGM_Article1.pdf Summary of Evidence:Weighing HRT Use After Breast Cancer by William Creasman, MD 2002 2002 Journal of Family Practice- Review of Observational Studies 16) www.ncbi.nlm.nih.gov/pubmed/12540332 J Fam Pract. 2002 Dec;51(12):1056-62. Cancer recurrence and mortality in women using hormone replacement therapy: meta-analysis. Meurer LN, Lená S. Department of Family and Community Medicine, Medical College of Wisconsin, Milwaukee, 53226, USA. We compared the risk of cancer recurrence and all-cause mortality among users and nonusers of estrogen replacement therapy (ERT) after the diagnosis of breast cancer. STUDY DESIGN: This was a systematic review of original research. Eligible studies were reviewed by 2 investigators who independently extracted data from each study according to a predetermined form and assessed each study for validity on standard characteristics. Meta-analyses were performed with Review Manager 4.1 to provide a summary of relative risks of cancer recurrence and mortality. POPULATION:Studies included 717 subjects who used hormone replacement therapy (HRT) at some time after their diagnosis of breast cancer, as well as 2545 subjects who did not use HRT. OUTCOMES MEASURED: Outcomes included breast cancer recurrence and all-cause mortality. RESULTS: Nine independent cohort studies and one 6-month pilot randomized controlled trial were identified. Studies were of variable quality. Breast cancer survivors using ERT experienced no increase in the risk of recurrence compared with controls (relative risk, 0.72; 95% confidence interval, 0.47-1.10) and had significantly fewer deaths (3.0%) than did the non-users (11.4%) over the combined study periods (relative risk, 0.18; 95% confidence interval, 0.10-0.31). All tests for heterogeneity were nonsignificant. CONCLUSIONS: Although limited by observational design, existing research does not support the universal withholding of ERT from well-informed women with a previous diagnosis of low-stage breast cancer. Long-term randomized controlled trials are needed. -------------------------------------- HABITS 2011 Brennan - Australia 17) www.miniseminaires.com/wp-content/uploads/DocsDPC/Suivicancerdusein.pdf Maturitas. 2011 Jun;69(2):106-12. Epub 2011 Apr 12. Overview of long term care of breast cancer survivors. Brennan ME, Houssami N. Screening and Test Evaluation Program (STEP), School of Public Health, Sydney Medical School, University of Sydney, Camperdown, Sydney, NSW, Australia. 6.2. Hormone replacement therapy The HABITS study,a randomised trial addressing the efficacy and safely of hormone replacement therapy after breastcancer treatment, was stopped after median follow-up of 2years a sit showed a significantly higher risk of breast cancer events in women randomised to treatment with HRT (clinician choice of therapy) compared to those not taking HRT (relative hazard (RH) risk 3.5;26 vs 7 events).There was a higher riskof new events in women with hormone receptor positive cancer (RH 4.8), those not taking tamox- ifen (RH3.7) and thosetaking HRT before breast cancer diagnosis (RH 6.9) [71]. In this trial,there was no significant difference in risk between combined preparations,oestrogen-only preparations and other preparations (suchastibolone) [71]. The Stockholm trial also randomised survivors to treatment with HRT or no HRT ;in this study there was no increased risk of recurrence in women in the HRT arm. One possible explanation for this is the higher pro- portion of women taking oestrogen-only preparations rather than continuous combined hormone preparations,indicating that the oestrogen-only preparations may be less hazardous in this group of women [72]. Based on these studies,systemic HRT is not recommended in breastcancer survivors. 2008 HABITS - Extended Follow Up RCT - increased rate in HRT users -Estradiol hemihydrate and norethisterone: Increased recurrence in BR CA survivors 18) www.ncbi.nlm.nih.gov/pubmed/18364505 J Natl Cancer Inst. 2008 Apr 2;100(7):475-82. Epub 2008 Mar 25. Increased risk of recurrence after hormone replacement therapy in breast cancer survivors. Holmberg L, Iversen OE, Rudenstam CM, Hammar M, Kumpulainen E, Jaskiewicz J, Jassem J, Dobaczewska D, Fjosne HE, Peralta O, Arriagada R, Holmqvist M, Maenpaa J; HABITS Study Group. Collaborators (25) Source Department of Surgical Sciences, Uppsala University, Uppsala, Sweden. BACKGROUND: Hormone replacement therapy (HT) is known to increase the risk of breast cancer in healthy women, but its effect on breast cancer risk in breast cancer survivors is less clear. The randomized HABITS study, which compared HT for menopausal symptoms with best management without hormones among women with previously treated breast cancer, was stopped early due to suspicions of an increased risk of new breast cancer events following HT. We present results after extended follow-up. METHODS: HABITS was a randomized, non-placebo-controlled noninferiority trial that aimed to be at a power of 80% to detect a 36% increase in the hazard ratio (HR) for a new breast cancer event following HT. Cox models were used to estimate relative risks of a breast cancer event, the maximum likelihood method was used to calculate 95% confidence intervals (CIs), and chi(2) tests were used to assess statistical significance, with all P values based on two-sided tests. The absolute risk of a new breast cancer event was estimated with the cumulative incidence function. Most patients who received HT were prescribed continuous combined or sequential estradiol hemihydrate and norethisterone. RESULTS: Of the 447 women randomly assigned, 442 could be followed for a median of 4 years. Thirty-nine of the 221 women in the HT arm and 17 of the 221 women in the control arm experienced a new breast cancer event (HR = 2.4, 95% CI = 1.3 to 4.2). Cumulative incidences at 5 years were 22.2% in the HT arm and 8.0% in the control arm. By the end of follow-up, six women in the HT arm had died of breast cancer and six were alive with distant metastases. In the control arm, five women had died of breast cancer and four had metastatic breast cancer (P = .51, log-rank test). CONCLUSION: After extended follow-up, there was a clinically and statistically significant increased risk of a new breast cancer event in survivors who took HT. 2004 - HABITS - Sweden - used norethisterone (known to be carcinogenic). 19) image.thelancet.com/extras/03let12260web.pdf www.ncbi.nlm.nih.gov/pubmed/14962527 Lancet. 2004 Feb 7;363(9407):453-5. HABITS (hormonal replacement therapy after breast cancer--is it safe?), a randomised comparison: trial stopped. Holmberg L, Anderson H; HABITS steering and data monitoring committees. Regional Oncologic Centre, University Hospital, SE-751 85 Uppsala, Sweden. In the 1990s, two randomised clinical trials started in Scandinavia addressing whether hormone replacement therapy (HRT) is safe for women with previous breast cancer. We report the findings of the safety analysis in HABITS (hormonal replacement therapy after breast cancer--is it safe?), an open randomised clinical trial with allocation to either HRT or best treatment without hormones. The main endpoint was any new breast cancer event. All analyses were done according to intention-to-treat. Until September, 2003, 434 women were randomised; 345 had at least one follow-up report. After a median follow-up of 2.1 years, 26 women in the HRT group and seven in the non-HRT group had a new breast-cancer event. All women with an event in the HRT group and two of those in the non-HRT group were exposed to HRT and most women had their event when on treatment. We decided that these findings indicated an unacceptable risk for women exposed to HRT in the HABITS trial, and the trial was terminated on Dec 17, 2003. Minimize use of progestin !!!! 2005 StockHolm Randomized Trial 20) jnci.oxfordjournals.org/content/97/7/533.long www.ncbi.nlm.nih.gov/pubmed/15812079 Journal of the National Cancer Institute 2005; 97(7):533–535. Menopausal hormone therapy after breast cancer: the Stockholm randomized trial. von Schoultz E, Rutqvist LE; Stockholm Breast Cancer Study Group. Department of Oncology, Karolinska University Hospital & Institute, Stockholm, Sweden. In 1997 two independent randomized clinical trials, Hormonal Replacement Therapy After Breast Cancer--Is It Safe? (HABITS; 434 patients) and the Stockholm trial (378 patients), were initiated in Sweden to compare menopausal hormone therapy with no menopausal hormone therapy after diagnosis of early-stage breast cancer. Much of the design of both studies was similar; however, a goal of the Stockholm protocol, not shared with the HABITS trial, was to minimize the use of progestogen combined with estrogen. The HABITS trial was prematurely stopped in December 2003, because, at a median follow-up of 2.1 years, the risk for recurrence of breast cancer among patients receiving menopausal hormone therapy was statistically significantly higher (relative hazard [RH] = 3.3, 95% confidence interval [CI] = 1.5 to 7.4) than among those receiving no treatment. In the Stockholm trial, however, at a median follow-up of 4.1 years, the risk of breast cancer recurrence was not associated with menopausal hormone therapy (RH = 0.82, 95% CI = 0.35 to 1.9). Statistically significant heterogeneity in the rate of recurrence was observed (P = .02; two-sided likelihood-ratio test) between the two studies, indicating that chance may not be the only explanation. Doses of estrogen and progestogen and treatment regimens for menopausal hormone therapy may be associated with the recurrence of breast cancer. MEGESTROL 2002 Natrajan -Megestrol - Megace 21) www.ncbi.nlm.nih.gov/pubmed/12193914 Am J Obstet Gynecol. 2002 Aug;187(2):289-94; discussion 294-5. Estrogen replacement therapy in patients with early breast cancer. Natrajan PK, Gambrell RD Jr.Reproductive Endocrinologists, Augusta, GA 30910, USA. Most physicians believe that estrogen replacement therapy is contraindicated once a patient is diagnosed with breast cancer. Recently, several studies have shown that estrogen replacement therapy may be safely used in patients with early breast cancer that has been treated successfully. These women can have severe menopausal symptoms and are at risk for osteoporosis. We reviewed the current status of women in our practice with breast cancer who received estrogen replacement therapy, who did not receive hormone replacement therapy, and who did not receive estrogenic hormone replacement therapy. STUDY DESIGN:The study group consisted of 123 women (mean age, 65.4 +/- 8.85 years) who were diagnosed with breast cancer in our practice, including 69 patients who received estrogen replacement therapy for < or = 32 years after diagnosis. The comparative groups were 22 women who used nonestrogenic hormones for < or = 18 years and 32 women who used no hormones for < or = 12 years. The group who did not receive estrogenic hormone replacement therapy received androgens with or without progestogens (such as megestrol acetate). Of the 63 living hormone users, 56 women are still being treated in our clinic, as are 15 of the 22 subjects who receive nonestrogenic hormone replacement therapy. Follow-up was done through the tumor registry at University Hospital; those patients whose tumor records were not current were contacted by telephone. RESULTS:There were 18 deaths in the 123 patients: 6 patients who received estrogen replacement therapy (8.69%), 2 patients who received nonestrogenic hormone replacement therapy (9.09%), and 10 patients who received no hormone replacement therapy (31.25%). Of the 18 deaths, 9 deaths were from breast cancer (mortality rate, 7.3%); 3 deaths were from lung cancer; 1 death was from endometrial cancer; 1 death was from myocardial infarction; 1 death was from renal failure; and 3 deaths were from cerebrovascular accidents. The 9 deaths from breast cancer included one patient who received nonestrogenic hormone replacement therapy (mortality rate, 4.5%), 6 patients who received no hormone replacement therapy (mortality rate, 11.3%), and 2 patients who received estrogen replacement therapy (mortality rate, 4.28%). The 9 non-breast cancer deaths included 4 patients who received estrogen replacement therapy (endometrial cancer [1 death], lung cancer [1 death], cerebrovascular accident [1 death], and renal failure [1 death]), 1 patient who did not receive estrogenic hormone replacement therapy group (myocardial infarction), and 4 patients who used no hormones (lung cancer, 2 deaths; stroke, 2 deaths). Carcinoma developed in one patient in the estrogen replacement therapy group in the contralateral breast after 4 years of hormone replacement therapy; she is living and well 2.5 years later with no evidence of disease. Metastatic breast cancer developed in one patient after 8 years of hormone replacement therapy; she is living with disease. CONCLUSION: Estrogen replacement therapy apparently does not increase either the risk of recurrence or of death in patients with early breast cancer. These patients may be offered estrogen replacement therapy after a full explanation of the benefits, risks, and controversies. 1999 Estradiol plus Megace (Megestrol Acetate -used as Br CA Rx) 22) http://www.sciencedirect.com/science/article/pii/S0002937899705508 Am J Obstet Gynecol. 1999 Aug;181(2):288-95. Estrogen replacement therapy in women with previous breast cancer. Natrajan PK, Soumakis K, Gambrell RD Jr. Department of Physiology, Medical College of Georgia, Augusta, Georgia, USA. OBJECTIVE: We sought to review the status of patients with breast cancer who were treated with estrogen replacement therapy and compare the results with those of nonestrogenic hormone users and women not treated with hormone replacement. STUDY DESIGN: The study group consisted of 76 patients with breast cancer, including 50 using estrogen replacement for up to 32 years, 8 using nonestrogenic hormone replacement for up to 6 years and followed for up to 11 years, and 18 using no hormones for up to 10 years. In addition to estrogen use, 40 of the 50 hormone users were treated with androgens, usually in the form of implantation of testosterone pellets. Forty-five subjects were also given progestogens, usually megestrol acetate 20 to 40 mg for 10 to 25 days each month. The 8 nonestrogen hormone users were treated with various combinations of testosterone pellets, tamoxifen, and progestogens. Forty-two of the 50 estrogen users are still being treated in our clinic, as are 2 of the 8 subjects using nonestrogen hormone. Follow-up was done through the tumor registry at University Hospital, and those whose tumor records were not current were telephoned. RESULTS: Of the 50 estrogen users, 3 have died (a mortality rate of 6%), and the rest have been followed for 6 months to 32 years, with a mean duration of follow-up of 83.3 +/- 8.81 months. One of the 8 nonestrogen hormone users has died (a mortality rate of 12.5%), and the rest have been followed for 2 to 11 years, with a mean duration of follow-up of 72.0 +/- 5. 93 months. Six of the 18 women not using hormone replacement have died (a mortality rate of 33.3%), and the rest have been followed for 6 months to 10 years, with a mean duration of follow-up of 50.5 +/- 6.01 months. CONCLUSION: Estrogen replacement therapy apparently does not increase either recurrences or mortality rates. Adding progestogens (Megace) may even decrease recurrences. Women with early breast cancer should be offered hormone replacement therapy after a full explanation of the benefits, risks, and controversies. ----------------------------------- BRCA GENE 2008 HRT in BRCA GENE women after OOPhorectomy or Menopause- less BR CA with HRT - Eisen 2008 23) jnci.oxfordjournals.org/content/100/19/1361.full.pdf+html Hormone Therapy and the Risk of Breast Cancer in BRCA1 Mutation Carriers Andrea Eisen, Jan Lubinski Affiliations of authors: Sunnybrook Regional Cancer Center, Toronto, Ontario, Canada (AE); Hereditary Cancer Center, Pomeranian Medical University, Szczecin, Poland (JL, JG); J Natl Cancer Inst. 2008 Oct 1;100(19):1361-7. Epub 2008 Sep 23. Hormone therapy and the risk of breast cancer in BRCA1 mutation carriers. Eisen A, Lubinski J, Gronwald J, Moller P, Lynch HT, Klijn J, Kim-Sing C, Neuhausen SL, Gilbert L, Ghadirian P, Manoukian S, Rennert G, Friedman E, Isaacs C, Rosen E, Rosen B, Daly M, Sun P, Narod SA; Hereditary Breast Cancer Clinical Study Group. Sunnybrook Regional Cancer Center, Toronto, Ontario, Canada. Hormone therapy (HT) is commonly given to women to alleviate the climacteric symptoms associated with menopause. There is concern that this treatment may increase the risk of breast cancer. The potential association of HT and breast cancer risk is of particular interest to women who carry a mutation in BRCA1 because they face a high lifetime risk of breast cancer and because many of these women take HT after undergoing prophylactic surgical oophorectomy at a young age. We conducted a matched case-control study of 472 postmenopausal women with a BRCA1 mutation to examine whether or not the use of HT is associated with subsequent risk of breast cancer. Breast cancer case patients and control subjects were matched with respect to age, age at menopause, and type of menopause (surgical or natural). Odds ratios (ORs) and 95% confidence intervals (CIs) were estimated with conditional logistic regression. Statistical tests were two-sided. RESULTS:In this group of BRCA1 mutation carriers, the adjusted OR for breast cancer associated with ever use of HT compared with never use was 0.58 (95% CI = 0.35 to 0.96; P = .03). In analyses by type of HT, an inverse association with breast cancer risk was observed with use of estrogen only (OR = 0.51, 95% CI = 0.27 to 0.98; P = .04); the association with use of estrogen plus progesterone was not statistically significant (OR = 0.66, 95% CI = 0.34 to 1.27; P = .21). CONCLUSION:Among postmenopausal women with a BRCA1 mutation, HT use was not associated with increased risk of breast cancer; indeed, in this population, it was associated with a decreased risk. 2008 BRCA GENE Carriers 24) jnci.oxfordjournals.org/content/100/19/1341.full jnci.oxfordjournals.org/content/100/19/1341.short JNCI J Natl Cancer Inst (2008) 100 (19): 1341-1343. JNCI Journal of the National Cancer Institute Advance Access published September 23, 2008 Menopausal Hormone Therapy in BRCA1 Mutation Carriers: Uncertainty and Caution Rowan T. Chlebowski , Ross L. Prentice Affiliations of authors: Los Angeles Biomedical Research Institute at Harbor- UCLA Medical Center, Torrance, CA (RTC); Division of Public Health Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA (RLP). Correspondence to: Rowan T. Chlebowski, MD, PhD, Los Angeles Biomedical Research Institute at Harbor-UCLA Medical Center, 1124 Carson St, Torrance, 2005 25) kksphotos.com/files/HRTAfterOoph.pdf jco.ascopubs.org/content/23/31/7804.long J Clin Oncol. 2005 Nov 1;23(31):7804-10. Epub 2005 Oct 11. Effect of short-term hormone replacement therapy on breast cancer risk reduction after bilateral prophylactic oophorectomy in BRCA1 and BRCA2 mutation carriers: the PROSE Study Group. Rebbeck TR, Friebel T, Wagner T, Lynch HT, Garber JE, Daly MB, Isaacs C, Olopade OI, Neuhausen SL, van 't Veer L, Eeles R, Evans DG, Tomlinson G, Matloff E, Narod SA, Eisen A, Domchek S, Armstrong K, Weber BL; PROSE Study Group. Source Center for Clinical Epidemiology and Biostatistics, The University of Pennsylvania School of Medicine, Philadelphia, 19104, USA. Purpose Bilateral prophylactic oophorectomy (BPO) is widely used for cancer risk reduction in women with BRCA1/2 mutations. Many premenopausal women choose to take hormone replacement therapy (HRT) after undergoing BPO to abrogate immediate symptoms of surgically-induced menopause. Thus, we evaluated whether the breast cancer risk reduction conferred by BPO in BRCA1/2 mutation carriers is altered by use of post-BPO HRT. Methods We identified a prospective cohort of 462 women with disease-associated germline BRCA1/2 mutations at 13 medical centers to evaluate breast cancer risk after BPO with and without HRT. We determined the incidence of breast cancer in 155 women who had undergone BPO and in 307 women who had not undergone BPO on whom we had complete information on HRT use. Postoperative follow-up was 3.6 years. Results Consistent with previous reports, BPO was significantly associated with breast cancer risk reduction overall (hazard ratio [HR] = 0.40; 95%CI, 0.18 to 0.92). Using mutation carriers without BPO or HRT as the referent group, HRT of any type after BPO did not significantly alter the reduction in breast cancer risk associated with BPO (HR = 0.37; 95% CI, 0.14 to 0.96). Conclusion Short-term HRT use does not negate the protective effect of BPO on subsequent breast cancer risk in BRCA1/2 mutation carriers. 2004 26) http://www.ncbi.nlm.nih.gov/pubmed/14981106 J Clin Oncol. 2004 Mar 15;22(6):1045-54. Epub 2004 Feb 23. Hormone replacement therapy and life expectancy after prophylactic oophorectomy in women with BRCA1/2 mutations: a decision analysis. Armstrong K, Schwartz JS, Randall T, Rubin SC, Weber B. Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA 19104-6021, USA. The decision about prophylactic oophorectomy is difficult for many premenopausal women with BRCA1/2 mutations because of concerns and controversy about the use of hormone replacement therapy (HRT) after oophorectomy. PATIENTS AND METHODS:A Markov decision analytic model used the most current epidemiologic data to assess the expected outcomes of prophylactic oophorectomy with or without HRT (to age 50 years or for life) in cohorts of women with BRCA1/2 mutations. Sensitivity analyses were conducted to assess the impact of alternative assumptions about effects of HRT, effects of prophylactic oophorectomy, and risks of cancer associated with BRCA1/2 mutations. RESULTS:In our model, prophylactic oophorectomy lengthened life expectancy in women with BRCA1/2 mutations, irrespective of whether HRT was used after oophorectomy. This gain ranged from 3.34 to 4.65 years, depending on age at oophorectomy. Use of HRT after oophorectomy was associated with relatively small changes in life expectancy (+0.17 to -0.34 years) when HRT was stopped at age 50, but larger decrements in life expectancy if HRT was continued for life (-0.79 to -1.09 years). HRT was associated with a gain in life expectancy of between 0.39 and 0.79 years for mutation carriers undergoing both prophylactic mastectomy and oophorectomy. CONCLUSION:On the basis of the results of this decision analysis, we recommend that women with BRCA1/2 mutations undergo prophylactic oophorectomy after completion of childbearing, decide about short-term HRT after oophorectomy based largely on quality-of-life issues rather than life expectancy, and, if using HRT, consider discontinuing treatment at the time of expected natural menopause, approximately age 50 years. ---------------------- ovarian ablation ovarian ablation 2011 27) www.ncbi.nlm.nih.gov/pubmed/21900112 J Clin Oncol. 2011 Oct 10;29(29):3939-42. Epub 2011 Sep 6. American Society of Clinical Oncology endorsement of the cancer care Ontario practice guideline on adjuvant ovarian ablation in the treatment of premenopausal women with early-stage invasive breast cancer. Griggs JJ, Somerfield MR, Anderson H, Henry NL, Hudis CA, Khatcheressian JL, Partridge AH, Prestrud AA, Davidson NE. 2004 -12 randomized trials of ovarian ablation in premenopausal women with BRCA 28) theoncologist.alphamedpress.org/content/9/5/507.long The Oncologist September 2004 vol. 9 no. 5 507-517 What Is the Role of Ovarian Ablation in the Management of Primary and Metastatic Breast Cancer Today? Tatiana M. Prowell and Nancy E. Davidson, M.D., The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, 1650 Orleans Street, Room 409, Baltimore, Maryland 21231-1000, USA. Telephone: 410-955-8489 a more recent meta-analysis by the Early Breast Cancer Trialists’ Collaborative Group of 12 properly designed randomized trials found significantly greater disease-free and overall survival rates for women under the age of 50, regardless of nodal status, receiving ovarian ablation as a single adjuvant therapy. Ovarian ablation was the original systemic therapy for breast cancer and has been in use for more than a hundred years, producing responses in approximately 30% of unselected women with metastatic breast cancer [1, 2], and in as many as 80% of women with steroid hormone receptor-positive (HR+) breast cancer [3, 4]. More recently, luteinizing hormone releasing hormone (LHRH) analogues, which act on the hypothalamic-pituitary-ovarian axis to suppress circulating estrogens to postmenopausal levels, have largely supplanted surgical and radiation-based approaches because of less morbidity and a lower likelihood of permanent amenorrhea, with the potential for restoration of fertility. Trials of adjuvant ovarian suppression have generally used either 2 [23] or 3 [26] years of treatment with an LHRH analogue, which produces comparable, and possibly even superior, outcomes to those obtained with CMF polychemotherapy in premenopausal HR+ patients. Ovarian ablation has long been established as an effective therapy for premenopausal women with metastatic breast cancer, with response rates ranging from 14%–70% in various studies [27]. Both the presence and degree of HR expression are strongly predictive of response to hormonal manipulation, with responses seen in approximately 60% of women having both ER+ and progesterone-receptor positive (PgR+) tumors, versus 30% in patients with either ER+ or PgR+ status alone [28]. Fewer than 10% of women with receptor negative (ER−/PgR−) disease respond to endocrine therapies [29]. Following the introduction of goserelin, a number of phase II trials of the monthly injections were conducted in premenopausal and perimenopausal women with advanced breast cancer. A meta-analysis of these trials containing more than 200 evaluable patients reported a median survival of 26.5 months, an overall response rate of 36% (44% in ER+ patients), and a median duration of response of 44 weeks [33, 34], which were comparable to the outcomes historically obtained with oophorectomy in similar patient populations. the combination of an LHRH analogue and tamoxifen may be superior to endocrine monotherapy in premenopausal HR+ women with advanced breast cancer and can be considered for first-line therapy. Approximately 25% of breast cancer patients are premenopausal at the time of diagnosis [41]; of these, 60% have HR+ tumors [42]. These women are regarded as potentially appropriate for hormonal manipulation. !!!!!!!!!!!!!!!!!!!!!!!!!!!!!! the EBCTCG meta-analysis [10]. This overview of 12 randomized controlled trials enrolling a total of 2,102 patients reported that women under the age of 50 with early invasive breast cancer who underwent oophorectomy or ovarian irradiation, experienced approximately a 25% relative reduction in the risks of recurrence and mortality at 15 years of follow-up compared with those receiving no adjuvant therapy. In summary, virtually all premenopausal women with early-stage HR+ breast cancer should receive adjuvant endocrine therapy. Combined endocrine therapy appears to be at least as effective as adjuvant CMF chemotherapy in this population. 1996 29) www.ncbi.nlm.nih.gov/pubmed/8898035?dopt=Abstract Lancet. 1996 Nov 2;348(9036):1189-96. Ovarian ablation in early breast cancer: overview of the randomised trials. Early Breast Cancer Trialists' Collaborative Group. [No authors listed] Among women with early breast cancer, the effects of ovarian ablation on recurrence and death have been assessed by several randomised trials that now have long follow-up. In this report, the Early Breast Cancer Trialists' Collaborative Group present their third 5-yearly systematic overview (meta-analysis), now with 15 years' follow-up. METHODS:In 1995, information was sought on each patient in any randomised trial of ovarian ablation or suppression versus control that began before 1990. Data were obtained for 12 of the 13 studies that assessed ovarian ablation by irradiation or surgery, all of which began before 1980, but not for the four studies that assessed ovarian suppression by drugs, all of which began after 1985. Menopausal status was not consistently defined across trials; therefore, the main analyses are limited to women aged under 50 (rather than "premenopausal") when randomised. Oestrogen receptors were measured only in the trials of ablation plus cytotoxic chemotherapy versus the same chemotherapy alone. FINDINGS:Among 2102 women aged under 50 when randomised, most of whom would have been premenopausal at diagnosis, 1130 deaths and an additional 153 recurrences were reported. 15-year survival was highly significantly improved among those allocated ovarian ablation (52.4 vs 46.1%, 6.3 [SD 2.3] fewer deaths per 100 women, logrank 2p = 0.001), as was recurrence-free survival (45.0 vs 39.0%, 2p = 0.0007). The numbers of events were too small for any subgroup analyses to be reliable. The benefit was, however, significant both for those with ("node positive") and for those without ("node negative") axillary spread when diagnosed. In the trials of ablation plus cytotoxic chemotherapy versus the same chemotherapy alone, the benefit appeared smaller (even for women with oestrogen receptors detected on the primary tumour) than in the trials of ablation in the absence of chemotherapy (where the observed survival improvements were about six per 100 node-negative women and 12 per 100 node-positive women). Among 1354 women aged 50 or over when randomised, most of whom would have been perimenopausal or postmenopausal, there was only a nonsignificant improvement in survival and recurrence-free survival. INTERPRETATION:In women aged under 50 with early breast cancer, ablation of functioning ovaries significantly improves long-term survival, at least in the absence of chemotherapy. Further randomised evidence is needed on the additional effects of ovarian ablation in the presence of other adjuvant treatments, and to assess the relevance of hormone-receptor measurements. 30) fds.oup.com/www.oup.com/pdf/13/9780199218141.pdf Goserelin KL Jones 31) www.ncbi.nlm.nih.gov/pubmed/21457974 Int J Gynaecol Obstet. 2011 Jun;113(3):222-4. Epub 2011 Apr 1. Laparoscopic salpingo-oophorectomy for ovarian ablation in women with hormone-sensitive breast cancer. Haldar K, Giamougiannis P, Wilson C, Crawford R. Department of Gynecological Oncology, University Hospital Llandough, Cardiff, UK. To evaluate institutional experiences regarding laparoscopic salpingo-oophorectomy in breast cancer patients and to compare the technique with gonadotropin-releasing hormone (GnRH) analogs among premenopausal women with hormone-sensitive breast cancer. METHODS:Between 2004 and 2009, 103 women with breast cancer underwent laparoscopic salpingo-oophorectomy at Addenbrooke's Hospital, Cambridge, UK. All relevant medical records-including reasons for salpingo-oophorectomy, peri-operative events, and subsequent follow-up-were reviewed. RESULTS:In the study period, 3 (2.9%) women experienced a recurrence of breast cancer but none had primary peritoneal/ovarian cancer within a median follow-up interval of 34 months (range, 0-70 months). No operative complications were noted among these women and all of them went home on the day of their operation. CONCLUSION:Laparoscopic salpingo-oophorectomy seems to be a safe, permanent, and cost-effective method of ovarian ablation compared with the use of GnRH analogs. Salpingo-oophorectomy also considerably reduces the risk of subsequent ovarian/fallopian tube malignancy in this high-risk population. 2007 32) www.ncbi.nlm.nih.gov/pubmed/17713096 Eur J Gynaecol Oncol. 2007;28(4):294-6. Laparoscopic oophorectomy either with or without hysterectomy for early breast cancer. Kucera E, Holub Z, Svobodova G. Department of Obstetrics and Gynecology, Institute of Care for Mother and Child, Prague, Czech Republic. The aim of this study was to assess the surgical results, complications and pathological findings of laparoscopic ovarian ablation either with or without hysterectomy in women with early-stage breast cancer (BC). METHODS:Ninety women in early breast cancer stage who underwent laparoscopic bilateral salpingo-oophorectomy (BSO) either with or without hysterectomy were identified in a retrospective study conducted between January 2000 and December 2006. Tamoxifen antiestrogen therapy was used prior to hysterectomy. RESULTS:Forty-eight consecutive patients underwent laparoscopic hysterectomy with bilateral salpingo-oophorectomy and 42 with ovarian ablation only. The mean operative time for the laparoscopic hysterectomy and bilateral salpingo-oophorectomy or BSO alone was 82 min and 47.8 min, respectively. Blood loss was minimal in both groups (range: 20-250 ml). The rate of postoperative complications was very low (4.4%). One of all ovaries removed by laparoscopy showed ovarian breast carcinoma metastasis. Histopathologic examination revealed concomitant findings of leiomyoma, adenomyosis or endometrial abnormalities in 64.5% of hysterectomy specimens. CONCLUSION:Our experience with ovarian ablation either with or without hysterectomy confirmed that the use of a minimally invasive technique is feasible. We assume that ovarian ablation and hysterectomy is an appropriate treatment for premenopausal women at risk (BRCA positive) or for patients with concomitant benign uterine pathology, treated with tamoxifen in first-line therapy. Removing the uterus allows women to take only estrogens rather than combination HRT. Further investigation into the indications of disease where laparoscopic ablative surgery is appropriate in the management of early breast cancer is needed. 2003 33) www.ncbi.nlm.nih.gov/pubmed/14998564 Surg Oncol. 2003 Dec;12(4):241-50. Ovarian ablation as a treatment for breast cancer. Sainsbury R.University College London W1W 7EJ, UK. Ovarian ablation is an effective treatment for premenopausal women with hormone receptor positive breast cancer. It can be achieved permanently by surgery or radiotherapy and reversibly by LhRH agonists. This paper discusses the evidence that it is an effective adjuvant therapy and defines the place of oophorectomy in the management of such patients. The achievement of an amenhorreic state is important and chemotherapy may well exert some of its effects by causing ovarian suppression. The use of LhRH agonists in managing such patients is discussed. 2006 34) www.ncbi.nlm.nih.gov/pubmed/16940812 Anticancer Drugs. 2006 Sep;17(8):999-1002. Combined ovarian ablation and aromatase inhibition as first-line therapy for hormone receptor-positive metastatic breast cancer in premenopausal women: report of three cases. El-Saghir NS, El-Hajj II, Makarem JA, Otrock ZK. American University of Beirut Medical Center, PO Box 113-6044, Beirut, Lebanon. Aromatase inhibitors have become well established for the treatment of postmenopausal women with hormone receptor-positive metastatic breast cancer and for adjuvant hormonal therapy for primary breast cancer. Benefit of aromatase inhibition has not yet been extended to premenopausal women. Ovarian ablation by oophorectomy, ovarian radiation or hormonal suppression is the initial recommended treatment for hormone receptor-positive metastatic breast cancer in premenopausal women. The addition of tamoxifen improves the benefit of ovarian ablation/ovarian suppression. Addition of aromatase inhibitors to luteinizing hormone-releasing hormone analogs has been reported to significantly decrease circulating estrogens and produce tumor responses in only a very small number of patients over the last 15 years. We treated three premenopausal patients with hormone receptor-positive metastatic breast cancer with combined oophorectomy or ovarian irradiation and anastrozole. One patient remained free of progression for 4 years, while the other two remained free of progression for more than 5 and 3 years, respectively. We also note that monthly zoledronic acid for 4 years produced sclerosis of vertebral body metastasis. We conclude that combined ovarian ablation and aromatase inhibition is a feasible treatment modality that deserves more attention and further investigation for hormone receptor-positive metastatic breast cancer in premenopausal women. Topical Progesterone Does NOT Cause Breast Cancer 35) http://ukpmc.ac.uk/abstract/MED/10403900 Percutaneous progesterone use and risk of breast cancer: results from a French cohort study of premenopausal women with benign breast disease. Plu-Bureau G, Lê MG, Thalabard JC, Sitruk-Ware R, Mauvais-Jarvis P INSERM, Gustave-Roussy Institute, Villejuif, France; Department of Reproductive Endocrinology, Necker Hospital, Paris, France. Cancer Detection and Prevention [1999, 23(4):290-6] Percutaneous progesterone topically applied on the breast has been proposed and widely used in the relief of mastalgia and benign breast disease by numerous gynecologists and general practitioners. However, its chronic use has never been evaluated in relation to breast cancer risk. The association between percutaneous progesterone use and the risk of breast cancer was evaluated in a cohort study of 1150 premenopausal French women with benign breast disease diagnosed in two breast clinics between 1976 and 1979. The follow-up accumulated 12,462 person-years. Percutaneous progesterone had been prescribed to 58% of the women. There was no association between breast cancer risk and the use of percutaneous progesterone (RR = 0.8; 95% confidence interval 0.4-1.6). Although the combined treatment of oral progestogens with percutaneous progesterone significantly decreased the risk of breast cancer (RR = 0.5; 95% confidence interval 0.2-0.9) as compared with nonusers, there was no significant difference in the risk of breast cancer in percutaneous progesterone users versus nonusers among oral progestogen users. Taken together, these results suggest at least an absence of deleterious effects caused by percutaneous progesterone use in women with benign breast disease. 1997 - Women with family history of breast cancer - Reduced Mortality for HRT users 36) www.ncbi.nlm.nih.gov/pubmed/9412302 Ann Intern Med. 1997 Dec 1;127(11):973-80. The role of hormone replacement therapy in the risk for breast cancer and total mortality in women with a family history of breast cancer.Sellers TA, Mink PJ, Cerhan JR, Zheng W, Anderson KE, Kushi LH, Folsom AR.Division of Epidemiology, University of Minnesota, Minneapolis 55454, USA. The risks and benefits of hormone replacement therapy (HRT) are of considerable interest and importance, especially in terms of whether they differ among subsets of women. OBJECTIVE: To determine whether HRT is associated with increased risks for breast cancer and total mortality in women with a family history of breast cancer. DESIGN: Prospective cohort study. SETTING: Population-based sample of midwestern post-menopausal women enrolled in an observational study of risk factors for cancer. PARTICIPANTS: Random sample of 41,837 female Iowa residents 55 to 69 years of age. MEASUREMENTS: Incidence rates of and relative risks for breast cancer (n = 1085) and total mortality (n = 2035) through 8 years of follow-up were calculated by using data from the State Health Registry of Iowa and the National Death Index. RESULTS: A family history of breast cancer was reported by 12.2% of the cohort at risk. Among women with a family history of breast cancer, those who currently used HRT and had done so for at least 5 years developed breast cancer at an age-adjusted annual rate of 61 cases per 10,000 person-years (95% CI, 28 to 94 cases); this rate was not statistically significantly higher than the rate in women who had never used HRT (46 cases per 10,000 person-years [CI, 36 to 55 cases]). Among women with a family history, those who used HRT had a significantly lower risk for total mortality than did women who had never used HRT (relative risk, 0.67 [CI, 0.51 to 0.89]), including total cancer-related mortality (relative risk, 0.75 [CI, 0.50 to 1.12]). The age-adjusted annual mortality rate for women using HRT for at least 5 years was 46 deaths per 10,000 person-years (CI, 19 to 74 deaths); this is roughly half the rate seen in women who had never used HRT (80 deaths per 10,000 person-years [CI, 69 to 92 deaths]). CONCLUSIONS: These data suggest that HRT use in women with a family history of breast cancer is not associated with a significantly increased incidence of breast cancer but is associated with a significantly reduced total mortality rate. ----- 2005 review-Collins - Canada - Progestins Increase Breast Cancer in Post Menopausal Women - Estrogen Alone Does NOT 37) humupd.oxfordjournals.org/content/11/6/545.long www.ncbi.nlm.nih.gov/pubmed/16150813 Hum Reprod Update. 2005 Nov-Dec;11(6):545-60. Epub 2005 Sep 8. Breast cancer risk with postmenopausal hormonal treatment. Collins JA, Blake JM, Crosignani PG. Source Department of Obstetrics and Gynecology, McMaster University, Hamilton, Ontario, Canada. Abstract This review was designed to determine from the best evidence whether there is an association between postmenopausal hormonal treatment and breast cancer risk. Also, if there is an association, does it vary according to duration and cessation of use, type of regimen, type of hormonal product or route of administration; whether there is a differential effect on risk of lobular and ductal cancer; and whether hormone treatment is associated with breast cancers that have better prognostic factors? Data sources for the review included Medline, the Cochrane Database of Systematic Reviews (Cochrane Library, 2005) and reference lists in the identified citations. Eligible citations addressed invasive breast cancer risk among postmenopausal women and involved use of the estrogen products with or without progestin that are used as treatment for menopausal symptoms. Abstracted data were demographic groupings, categories of hormone use, categories of breast cancer, two-by-two tables of exposure and outcome and adjusted odds ratios, relative risks (RRs) or hazard rates. Average estimates of risk were weighted by the inverse variance method, or if heterogeneous, using a random effects model. The average risk of invasive breast cancer with estrogen use was 0.79 [95% confidence interval (95% CI) = 0.61-1.02] in four randomized trials involving 12 643 women. The average breast cancer risk with estrogen-progestin use was 1.24 (95% CI = 1.03-1.50) in four randomized trials involving 19 756 women. The average risks reported in recent epidemiological studies were higher: 1.18 (95% CI = 1.01-1.38) with current use of estrogen alone and 1.70 (95% CI = 1.36-2.17) with current use of estrogen-progestin. The association of breast cancer with current use was stronger than the association with ever use, which includes past use. For past use, the increased breast cancer risk diminished soon after discontinuing hormones and normalized within 5 years. Reasonably adequate data do not show that breast cancer risk varies significantly with different types of estrogen or progestin preparations, lower dosages or different routes of administration, although there is a small difference between sequential and continuous progestin regimens. Epidemiological studies indicate that estrogen-progestin use increases risk of lobular more than ductal breast cancer, but the number of studies and cases of lobular cancer remains limited. Among important prognostic factors, the stage and grade in breast cancers associated with hormone use [corrected] do not differ significantly from those in non-users, but breast cancers in estrogen-progestin users are significantly more likely to be estrogen receptor (ER) positive. In conclusion, valid evidence from randomized controlled trials (RCTs) indicates that breast cancer risk is increased with estrogen-progestin use more than with estrogen alone. Epidemiological evidence involving more than 1.5 million women agrees broadly with the trial findings. Although new studies are unlikely to alter the key findings about overall breast cancer risk, research is needed, however, to determine the role of progestin, evaluate the risk of lobular cancer and delineate effects of hormone use on receptor presence, prognosis and mortality in breast cancer. -------------------------------------- 2005 Review of Literature - Discrepant Findings 2005 Meta-Analysis-Col-Brown Medical school 38) www.ncbi.nlm.nih.gov/pmc/articles/PMC1175064/?tool=pubmed www.ncbi.nlm.nih.gov/pubmed/15987460 breast-cancer-research.com/content/7/4/R535 Breast Cancer Res. 2005;7(4):R535-40. Epub 2005 May 19. Menopausal hormone therapy after breast cancer: a meta-analysis and critical appraisal of the evidence. Col NF, Kim JA, Chlebowski RT. Source Brown Medical School, Providence, Rhode Island, USA. Menopausal hormone therapy (HT) is typically withheld from breast cancer survivors because of concerns about risk for recurrence. Our objectives were to estimate the effects of HT on recurrence in breast cancer survivors and to examine the reliability of these estimates. Methods In a systematic review of the literature we identified all reports of HT use in breast cancer survivors that included comparison groups. Study design features that might affect selection of participants, detection of recurrence, and manuscript publication were assessed. The relative risks for breast cancer recurrence associated with HT were combined with random effects models. Results Two randomized and eight observational studies included 1,316 breast cancer survivors who used HT and 2,839 nonusers. In the observational studies, HT users were younger and more commonly node negative; only two reported balanced restaging for HT and control groups. Randomized trials suggest that HT increased the risk for recurrence (relative risk 3.41, 95% confidence interval 1.59–7.33), whereas observational studies suggest that HT decreased this risk (relative risk 0.64, 95% confidence interval 0.50–0.82). Conclusion: Results from observational studies of HT conducted in breast cancer survivors are discrepant with results from randomized trials. Observational studies of HT use in breast cancer survivors have design limitations that cannot be controlled for using standard statistical methods. Therefore, the randomized clinical trial data provide the only reliable estimates of the effect of HT use on recurrence risks in breast cancer survivors. -------------------------------- 2006 BATUR - Cleveland Clinic - Review of ALL studies- HRT users had decreased recurrence and decreased mortality 39) www.ncbi.nlm.nih.gov/pubmed/16368466 Maturitas. 2006 Jan 20;53(2):123-32. Menopausal hormone therapy (HT) in patients with breast cancer. Batur P, Blixen CE, Moore HC, Thacker HL, Xu M. Department of Internal Medicine, Section of Women's Health Cleveland Clinic Foundation, Crown Centre II, Independence, OH 44131, USA. To assess the effect of menopausal hormone therapy (HT) on reoccurrence, cancer-related mortality, and overall mortality after a diagnosis of breast cancer. METHODS:We performed a quantitative review of all studies reporting experience with menopausal HT for symptomatic use after a diagnosis of breast cancer. Rates of reoccurrence, cancer-related mortality, and overall mortality were calculated in this entire group. A subgroup analysis was performed in studies using a control population to assess the odds ratio of cancer reoccurrence and mortality in hormone users versus non-users. RESULTS: Fifteen studies encompassing 1416 breast cancer survivors using HT were identified. Seven studies included a control group comprised of 1998 patients. Among the 1416 HT users, reoccurrence was noted in 10.0% (95% CI: 8.4-11.6%). Cancer-related mortality occurred at a rate of 2.6% (95% CI: 1.8-3.7%), while overall mortality was 4.5% (95% CI: 3.4-5.8%). "Compared to non-users, patients using HT had a decreased chance of reoccurrence and cancer-related mortality with combined odds ratio of 0.5 (95% CI: 0.2-0.7) and 0.3 (95% CI: 0.0-0.6), respectively." CONCLUSIONS: In our review, menopausal HT use in breast cancer survivors was not associated with increased cancer reoccurrence, cancer-related mortality or total mortality. Despite conflicting opinions on this issue, it is important for primary care physicians to feel comfortable medically managing the increasing number of breast cancer survivors. In the subset of women with severe menopausal symptoms, HT options should be reviewed if non-hormonal methods are ineffective. Future trials should focus on better ways to identify breast cancer survivors who may safely benefit from HT versus those who have a substantial risk of reoccurrence with HT use. ---------------------------- 2009 Reply to Creaseman by Labriola, 40) www.cancernetwork.com/display-cme/article/10165/1486375 2009 - Letter to the Editor Hormone Replacement and Breast Cancer Risk: The Authors Reply By Dan Labriola, ND Kathleen Pratt, ND Patrick Bufi, ND Northwest Natural Health®, A Specialty Care Clinic and Swedish Cancer Institute, Swedish Medical Center Seattle, Washington | November 12, 2009 Our commentary in the July 2009 issue of ONCOLOGY concluded that the current level of evidence for safety and efficacy of “natural” hormone replacement therapy (NHRT) is not conclusive. In terms of safety, the majority of data suggests that NHRTs demonstrate risks similar to those of conventional hormone replacement therapy (HRT). Efficacy trials of NHRTs have produced mixed and sometimes contradictory results. We further suggested that the administration of hormone therapy rely on evidence-based clinical judgment; NHRT advice to women should be based on the same risk/benefit assessment that would be used when considering conventional HRT. Drs. Creasman and DiSaia use this as a segue in their Letter to the Editor to defend the use of HRT for women, taking the position that there is really a lot of fuss about nothing with HRT, and if NHRT is the same, no problem. They argue that for breast cancer survivors, “In view of the present data, we feel it is important for women to know there are choices, and current data would suggest that there is no increased risk of recurrence with HRT.” (MORE: ‘Natural’ Hormone Replacement and Breast Cancer Risk: Evidence for Safety and Efficacy) Debatable Defense Their first defense of HRT is a 2002 citation by Chlebowski et al,[1] but the writers fail to mention the fact that these authors concluded, “Relatively short-term combined estrogen plus progestin use increases incident breast cancers, which are diagnosed at a more advanced stage compared with placebo use, and also substantially increases the percentage of women with abnormal mammograms. These results suggest estrogen plus progestin may stimulate breast cancer growth and hinder breast cancer diagnosis.” They go on to cite other studies including a small (n = 43) 1985 trial by Matelski et al.[2] The writers conclude from this citation that “In the 1970s and early 1980s, several prospective randomized studies compared estrogen with tamoxifen(Drug information on tamoxifen) in such women. The results were similar.” Their conclusion is not shared by the evidence. Even the authors of their citation disagree, concluding that “Initial hormonal therapy with tamoxifen in postmenopausal patients with advanced breast cancer and ERP status positive or unknown is superior to primary estrogen treatment.” The writers also comment on the HABITS trial,[3] which was stopped as a result of increased breast cancer risk in the HRT arm and the Stockholm trial.[4] They conclude “In view of the present data, we feel it is important for women to know there are choices, and current data would suggest that there is no increased risk of recurrence with HRT.” Once again, their conclusions are not consistent with the evidence or other well considered analyses. Further Evidence Prentice et al[5] examined the effects of daily 0.625-mg conjugated equine estrogens (Drug information on estrogens) plus 2.5-mg medroxyprogesterone (Drug information on medroxyprogesterone) acetate in relation to both prior hormone therapy and time from menopause to first use of postmenopausal hormone therapy (“gap time”) in the Women’s Health Initiative (WHI) trial and in a corresponding subset of the WHI observational study on postmenopausal women with a uterus enrolled at 40 US clinical centers during 1993–1998. The authors found that hazard ratios agreed between the two cohorts at a specified gap time and time from hormone therapy. They determined that the “Combined trial and observational study data support an adverse effect on breast cancer risk.” They further concluded, “The WHI clinical trial and observational study each support an adverse effect of daily 0.625-mg conjugated equine estrogen plus 2.5-mg medroxyprogesterone acetate on breast cancer. Women who initiate treatment soon after menopause and continue for many years appear to be at particularly high risk.” As if this weren’t enough, a recent review by Chlebowski et al[6] showed a significant increase in deaths (not incidence) from lung cancer for women receiving estrogen plus progestin compared to placebo controls enrolled in the WHI. Conclusion The writers’ argument in favor of the safety of HRT is not supported by the evidence, including their own references. Our conclusions in the July 2009 ONCOLOGY Commentary remain unchanged—namely that HRT (including NHRT) should be based on a balanced risk/benefit assessment and that high-risk patients including survivors of hormone-driven breast cancer are not appropriate candidates for HRT. As new clinical trials increase our body of knowledge, we will hopefully have more tools and flexibility when making clinical judgments, but at this time we must not lose sight of the principle of “do no harm.” -------------------- Estriol 41) www.ncbi.nlm.nih.gov/pubmed/9577246 Altern Med Rev. 1998 Apr;3(2):101-13. Estriol: safety and efficacy. Head KA. Free FIll Text Abstract While conventional hormone replacement therapy provides certain benefits, it is not without significant risks. Estriol has been found to provide some of the protection without the risks associated with stronger estrogens. Depending upon the situation, estriol may exert either agonistic or antagonistic effects on estrogen. Estriol appears to be effective at controlling symptoms of menopause, including hot flashes, insomnia, vaginal dryness, and frequent urinary tract infections. Results of research on its bone-density-maintaining effects have been contradictory, with the most promising results coming from Japanese studies. Estriol's effect on cardiac risk factors has also been somewhat equivocal; however, unlike conventional estrogen prescriptions, it does not seem to contribute to hypertension. Although estriol appears to be much safer than estrone or estradiol, its continuous use in high doses may have a stimulatory effect on both breast and endometrial tissue. 42) www.ncbi.nlm.nih.gov/pubmed/3119187 Cancer. 1987 Dec 15;60(12):2873-81. Antimammary carcinogenic activity of 17-alpha-ethinyl estriol. Lemon HM.Department of Internal Medicine, University of Nebraska Medical Center, Omaha 68105. Abstract Both initiation and promotion of dimethylbenz(a)anthracene (DMBA)-induced mammary carcinogenesis were inhibited by prophylactic therapy for 1 to 7 months using 17-alpha-ethinyl-estriol in doses as low as 1.0 microgram/d administered to intact virgin female Sprague-Dawley rats at 35 to 65 days of age. Administration of 638-micrograms single or multiple doses 2 to 3 weeks before DMBA induced a 75% to 85% reduction in cancer incidence after 1 year (P less than 0.001). When treatment was begun 2 weeks after DMBA, 1.0 microgram/d infused for 84 days resulted in a 44% reduction in incidence, with higher-dose, more prolonged therapy achieving a 73% reduction, equal to the reduction in carcinoma incidence observed after ovariectomy. Biopsies of nontumorous mammary glands showed a positive correlation between prelactational lobuloalveolar hyperplasia, hormone dose, and reduction in incidence of mammary carcinoma. Similar treatment with 17-alpha-ethinyl-estradiol-17B and diethylstilbestrol did not inhibit the 90% to 100% incidence of carcinoma observed in DMBA-treated control rats, and induced lactational hyperplasia in mammary gland biopsies. Continuous ethinyl estriol infusion subcutaneous (sc) in 2.5 to 7.5 micrograms daily dosage significantly increased uterine weights by as much as 10% to 46% after 2 to 4 weeks. At the time of mammary neoplasm development when rats were necropsied, no significant difference was observed in uterine weights between rats receiving 638 micrograms/mo in a readily soluble pellet implant, and uterine weights of control rats. Ethinyl estriol given seven times monthly in 638-micrograms bolus doses was more inhibitory of mammary carcinogenesis than estriol after a year (P less than 0.1 greater than 0.05). Short-term intermittent administration of ethinyl estriol to young nulliparous women may offer a method of simulating the differentiating effect of pregnancy on mammary tissues, increasing durable resistance to carcinogenesis. 43) www.ncbi.nlm.nih.gov/pubmed/6996403 Acta Endocrinol Suppl (Copenh). 1980;233:17-27. Pathophysiologic considerations in the treatment of menopausal patients with oestrogens; the role of oestriol in the prevention of mammary carcinoma. Lemon HM.At menopause, several abnormalities in oestrogen metabolism have been reported, which may increase the likelihood of cancer development in the breast or uterus following oestrone or oestradiol-17 beta supplementation. Occult hypothyroidism reduces the rate of oestrogen inactivation by C2 hydroxylation, and 15-20% of women have low rates of C16 hydroxylation to oestriol. Reduced sex hormone binding globulin concentration occurs in association with obesity, thereby increasing the biologically active unbound fraction of oestradiol in plasma. Since oestriol undergoes minimal metabolism after absorption, does not bind to sex hormone binding globulin, and has an anti-oestradiol action by decreasing the duration of nuclear binding of oestradiol-receptor proteins, it is less likely to induce proliferative changes in target organs of cancer-prone women than oestrone or oestradiol. Intermittent non-conjugated oestriol treatment has demonstrated the most significant anti-mammary carcinogenic activity of 22 tested compounds as well as anti-uterotropic activity in intact female Sprague Dawley rats fed either of two dissimilar carcinogens (7, 12 dimethylbenz(a) anthracene, procarbazine) and followed for their natural life span. The protective effect was specific for mammary carcinomas only and has been decreased in rats with a 20% increase in growth curves. Clinical experience thus far with oral oestriol therapy of post-menopausal women has indicated little hazard of cancer development. 44) jama.jamanetwork.com/article.aspx?articleid=357461 JAMA. 1978 Jan 2;239(1):29-30. Estriol, the forgotten estrogen? Follingstad AH. 45) www.ncbi.nlm.nih.gov/pubmed/97100 Front Horm Res. 1977;5:155-73. Clinical and experimental aspects of the anti-mammary carinogenic activity of estriol. Lemon HM. Abstract Intermittent implantation of 600--1,300 microgram estriol subcutaneously beginning 48 h before oral administration of 7,12-dimethylbenz(a)anthracene or procarbazine prevents development of 80--90% of carcinomas of the breast occurring during the natural life span of the intact female Sprague-Dawley rat. Some estriol precursors were less inhibitory of breast cancer development among 23 other estrogens and androgens, progestins and glucocorticoids tested. More frequent or lower estriol doses than 100--200 microgram/kg/24 h every 2 months were less inhibitory of breast carcinogenesis. No other types of neoplasms were reduced in incidence by estriol implants, which also reduced uterine weights by 20--25%. Intermittent substitution of estriol for estrone or estradiol in the nuclear receptor complexes of target cells probably accounts for these observations, which resemble the effect of castration in reducing breast cancer incidence. Human studies indicate excellent tolerance for oral estriol doses of 10--200 microgram/kg/24 h, which may correct subnormal estriol/estrone + estradiol urinary quotients associated with elevated risk of breast carcinogenesis in epidemiologic investigations. 46) cancerres.aacrjournals.org/content/35/5/1341 Cancer Res. 1975 May;35(5):1341-53. Estriol prevention of mammary carcinoma induced by 7,12-dimethylbenzanthracene and procarbazine. Lemon HM. Abstract The concentration of estrogenic, androgenic, progestational, and adrenocortical steroid hormones in body fluids of mature intact Sprague-Dawley female rats was increased by s.c. implantation of 5 to 7 mg NaCl pellets containing 1 to 20% steroid 48 hr before administration p.o. of either 7,12-dimethylbenz(a) anthracene or procarbazine. The incidence of rats developing one or more mammary carcinomas in each treated group was compared to that ovserved in simultaneously treated groups receiving only the carcinogen, steroid, or no treatment whatsoever, with weekly observation of all rats until palpably growing tumors were biopsied and proven carcinomatous or until death occurred from other causes determined by autopsy. A total of 105 untreated or steroid-implanted rats followed to death (234 to 256 days median observation) developed no breast carcinomas. Rats fed either of the carcinogens developed initial evidence of breast carcinoma, after 136 to 156 days median observation, in 51 to 57% of 318 total treated rats. Nonbreast carcinomas and sarcomas developed in 5 to 10% of the carcinogen-treated rats. 47) www.ncbi.nlm.nih.gov/pubmed/6773286 Acta Endocrinol Suppl (Copenh). 1980;233:45-50. The significance of oestriol in the management of the post-menopause. Tzingounis VA, Aksu MF, Greenblatt RB. Abstract Oestrogen replacement therapy relieves many post-menopausal symptoms and has been successfully employed clinically for this purpose for more than four decades. Recently the alleged relationship between oestrogens and cancer has stimulated a re-evaluation of an old oestrogen preparation, oestriol (E3). The dosages of E3 employed appear to vary considerably, and the need was felt to establish the dosage on a scientific basis. Accordingly in the study reported here E3 was administered in various dosages (2, 4, 6, and 8 mg/d) to 52 symptomatic post-menopausal women as oestrogen replacement therapy for a six-month period. Assays of follicle-stimulating hormone (FSH), luteinizing hormone (LH), oestrone (E1) and oestradiol (E2) were performed before and during therapy and vaginal cytology, cervical mucus and endometrial studies were performed during the period of administration. The clinical effectiveness of E3 was found to be directly related to dosage. E3 did not induce endometrial proliferation and proved a poor suppressor of FSH and LH. The ability of oestriol to relieve vasomotor instability and to improve vaginal maturation without inducing notable side effects is sufficient reason for it to be included in the management of the post-menopausal syndrome. 48) www.ncbi.nlm.nih.gov/pubmed/6789033 Maturitas. 1981 Mar;3(1):47-53. Oestrogens, gonadotropins and prolactin after intra-vaginal administration of oestriol in post-menopausal women. Keller PJ, Riedmann R, Fischer M, Gerber C. Abstract Serum total oestrone, 17 beta-oestradiol and oestriol concentrations and FSH, LH and prolactin values were measured radioimmunologically in post-menopausal women before and after intra-vaginal application of 0.5 mg oestriol. While oestrone and oestradiol were not altered, there was a 3100% increase in the mean oestriol values within 1 or 2 h; pre-treatment levels were again reached 8 h later. Both gonadotropins were moderately decreased, the serum prolactin values appeared to be slightly elevated. Repeated intra-vaginal application of oestriol resulted in a significant rise of the mean serum oestriol levels while the other oestrogens remained unchanged. The same was true for FSH and LH, a considerable negative feedback was therefore excluded. Again there seemed to be a slight rise of the prolactin secretion. It was concluded that intra-vaginal administration of oestriol is a most suitable local and systemic oestrogen replacement therapy, which is more effective than the oral regimen. ------------------------------------ 2009 creaseman and desaia www.cancernetwork.com/display/article/10165/1486356 Hormone Replacement and Breast Cancer Risk: Reconsidering the Data By William T. Creasman, MD Department of Obstetrics and Gynecology Medical University of South Carolina Charleston, South Carolina Philip J. DiSaia, MD Department of Obstetrics and Gynecology University of California, Irvine Irvine, California | November 12, 2009 In many instances, women are told that HRT is absolutely contraindicated, yet we are unaware of any clinical data to substantiate that statement. In view of the present data, we feel it is important for women to know there are choices, and current data would suggest that there is no increased risk of recurrence with HRT. ------------------------------------------------- 2011 Howell www.ncbi.nlm.nih.gov/pubmed/21253794 Recent Results Cancer Res. 2011;188:115-24. Hormone replacement therapy and breast cancer. Howell A, Evans GD.Genesis Prevention Centre, University Hospital of South Manchester, Manchester, UK. There is evidence that hormone replacement therapy (HRT) may both stimulate and inhibit breast cancers, giving rise to a spectrum of activities, which are frequently hard to understand. Here we summarise the evidence for these paradoxical effects and, given the current data, attempt to give an indication where it may or may not be appropriate to prescribe HRT.It is clear that administration of oestrogen-progestin (E-P) and oestrogen alone (E) HRT is sufficient to stimulate the growth of overt breast tumours in women since withdrawal of HRT results in reduction of proliferation of primary tumours and withdrawal responses in metastatic tumours. E-P, E including tibolone are associated with increased local and distant relapse when given after surgery for breast cancer. For women given HRT who do not have breast cancer the only large randomised trial (WHI) of E-P or E versus placebo has produced some expected and also paradoxical results. E-P increases breast cancer risk as previously shown in observational studies. Risk is increased, particularly in women known to be compliant. Conversely, E either has no effect or reduces breast cancer risk consistent with some but not all observational studies. Two observational studies report a decrease or at least no increase in risk when E-P or E are given after oophorectomy in young women with BRCA1/2 mutations. Early oophorectomy increases death rates from cardiovascular and other conditions and there is evidence that this may be reversed by the use of E post-oophorectomy. HRT may thus reduce the risk of breast cancer and other diseases (e.g., cardiovascular) in young women and increase or decrease them in older women. 2011 Liotta- Cleveland Clinic www.ncbi.nlm.nih.gov/pubmed/21278517 Clin Obstet Gynecol. 2011 Mar;54(1):173-9. Hormone replacement after breast cancer: is it safe? Liotta M, Escobar PF.Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, The Cleveland Clinic, Cleveland, Ohio, USA. The use of hormone therapy for climacteric symptoms in patients with breast cancer has become a significant and important point of discussion due in part to the improved survival from this disease in recent years. "There is a theoretic risk that exogenous hormones will stimulate the growth of microscopic disease and lead to decreased survival and increased recurrence." In addition, 2 large studies have shown that there is an association between hormone therapy and breast cancer risk in women without an earlier history of breast cancer. Other studies suggest that estrogen alone may have a superior safety profile than estrogen and progesterone in combination. "Hormone therapy could be justified for improvement of quality of life when other options have failed and the patient is informed of the risks." 2011 Brennan - Austalia www.miniseminaires.com/wp-content/uploads/DocsDPC/Suivicancerdusein.pdf Maturitas. 2011 Jun;69(2):106-12. Epub 2011 Apr 12. Overview of long term care of breast cancer survivors. Brennan ME, Houssami N. Screening and Test Evaluation Program (STEP), School of Public Health, Sydney Medical School, University of Sydney, Camperdown, Sydney, NSW, Australia. 6.2. Hormone replacement therapy The HABITS study,a randomised trial addressing the efficacy and safely of hormonereplacement therapy after breastcancer treatment, wasstopped aftermedian follow-upof 2years a sit showed asignificantlyhigherriskofbreastcancereventsinwomen randomised totreatmentwithHRT(clinicianchoiceoftherapy) compared tothosenottakingHRT(relativehazard(RH)risk3.5;26 vs 7events).Therewasahigherriskofneweventsinwomenwith hormone receptorpositivecancer(RH4.8),thosenottakingtamox- ifen (RH3.7)andthosetakingHRTbeforebreastcancerdiagnosis (RH 6.9) [71]. Inthistrial,therewasnosignificantdifferencein risk betweencombinedpreparations,oestrogen-onlypreparations and otherpreparations(suchastibolone) [71]. TheStockholmtrial also randomisedsurvivorstotreatmentwithHRTornoHRT;in this studytherewas no increasedriskofrecurrence in women in the HRTarm.Onepossibleexplanationforthisisthe higher pro- portion ofwomentakingoestrogen-onlypreparationsratherthan continuous combinedhormonepreparations,indicatingthatthe oestrogen-only preparationsmaybelesshazardousinthisgroup of women [72]. The LIBERATE randomised trial(over3000women randomised) showedanincreasedriskofrecurrenceinwomentak- ing tibolonevsplaceboforvasomotorsymptoms [73]. Based on these studies,systemic HRT is not recommended in breastcancer survivors. The use of vaginal oestrogens is discussedbelow. 2011 King UK -Premature Menopause- HRT contraindicated for premenopausal ER positive BRCA www.ncbi.nlm.nih.gov/pubmed/21561765 Eur J Cancer. 2011 Jul;47(11):1623-32. Epub 2011 May 9. Hormone replacement therapy and women with premature menopause--a cancer survivorship issue. King J, Wynne CH, Assersohn L, Jones A. Oncology Department, Royal Free Hampstead NHS Trust, Pond Street, London NW3 2PF, United Kingdom. The importance of addressing survivorship issues has been emphasised in recent years. As cancer therapies improve there is a growing population of cancer survivors, which includes many women with premature menopause. Women who are premenopausal at the time of their cancer diagnosis may have specific survivorship issues to be addressed, including infertility, early menopause and sexual dysfunction. These factors can continue have a significant impact on the quality of life of these patients at long term follow up. Data for this Review were identified by searches of MEDLINE, PubMed, and references from relevant articles using the search terms 'HRT', 'women/female cancer/tumour', 'menopause' and 'survivorship'. Abstracts and reports from meetings were excluded. Only papers published in English between 1980 and 2010 were included. The aims of this review are to: • Address the hormonal factors which impact on cancer survivorship for premenopausal women • Review the debate for the role of hormone replacement therapy (HRT) in cancer survivors • Provide information for physicians and patients regarding the management of hormonally driven survivorship issues (for different tumour types), based on current evidence The recommendations for practice are that HRT may be offered for the alleviation of vasomotor symptoms in cancer survivors who undergo premature menopause up to the age of natural menopause (51 years in the UK). "HRT (including vaginal oestrogen preparations) is contraindicated in survivors of oestrogen receptor positive breast cancer and low grade endometrial leiomyosarcoma, where non-HRT alternatives should be considered to alleviate symptoms." ------------------------------------------------- Joseph Ragaz MD Oncologist Dec 2010 WHI DATA re-evaluated www.breastcancerchoices.org/files/ragaz_hrt_aacr_san_antonio_news_release_dec_2010.pdf News Release Dec 9 2010 Estrogen Alone is Effective for Reducing Breast Cancer Risk www.drjosephragaz.com/oncology-news.php Oncology News & Updates: December 16, 2010 Estrogen Alone is Effective for Reducing Breast Cancer Risk Exogenous estrogen (administered as HRT) reduces breast cancer rates. HRT based on estrogen alone helps manage menopausal symptoms. More data are needed to elaborate on estrogen’s role in chemoprevention. SAN ANTONIO - While endogenous estrogen (i.e., estrogen produced by ovaries and by other tissues) does have a well-known carcinogenic impact, hormone replacement therapy (HRT) utilizing estrogen alone (the exogenous estrogen) provides a protective effect in reducing breast cancer risk, according to study results presented at the 33rd Annual CTRC-AACR San Antonio Breast Cancer Symposium, held Dec. 8-12. “Our analysis suggests that, contrary to previous thinking, there is substantial value in bringing HRT with estrogen alone to the guidelines. The data show that for selected women it is not only safe, but potentially beneficial for breast cancer, as well as for many other aspects of women’s health,” said lead researcher Joseph Ragaz, M.D., medical oncologist and clinical professor in the faculty of medicine, School of Population and Public Health at The University of British Columbia, Vancouver, BC, Canada. Dr Ragaz Video www.oncologytube.com/index.php?page=videos§ion=view&vid_id=100845 SABCS 2010: Dr. Joseph Ragaz MD, what will be the impact on future trials from the data pulled from Women's Health Initiative about Estrogen-Only Hormone Therapy? -------------------- --------------------------------------------- 2008 HABITS - Extended Follow Up RCT - increased rate in HRT users -Estradiol hemihydrate and norethisterone: Increased recurrence in BR CA survivors www.ncbi.nlm.nih.gov/pubmed/18364505 J Natl Cancer Inst. 2008 Apr 2;100(7):475-82. Epub 2008 Mar 25. Increased risk of recurrence after hormone replacement therapy in breast cancer survivors. Holmberg L, Iversen OE, Rudenstam CM, Hammar M, Kumpulainen E, Jaskiewicz J, Jassem J, Dobaczewska D, Fjosne HE, Peralta O, Arriagada R, Holmqvist M, Maenpaa J; HABITS Study Group. Collaborators (25) Source Department of Surgical Sciences, Uppsala University, Uppsala, Sweden. BACKGROUND: Hormone replacement therapy (HT) is known to increase the risk of breast cancer in healthy women, but its effect on breast cancer risk in breast cancer survivors is less clear. The randomized HABITS study, which compared HT for menopausal symptoms with best management without hormones among women with previously treated breast cancer, was stopped early due to suspicions of an increased risk of new breast cancer events following HT. We present results after extended follow-up. METHODS: HABITS was a randomized, non-placebo-controlled noninferiority trial that aimed to be at a power of 80% to detect a 36% increase in the hazard ratio (HR) for a new breast cancer event following HT. Cox models were used to estimate relative risks of a breast cancer event, the maximum likelihood method was used to calculate 95% confidence intervals (CIs), and chi(2) tests were used to assess statistical significance, with all P values based on two-sided tests. The absolute risk of a new breast cancer event was estimated with the cumulative incidence function. Most patients who received HT were prescribed continuous combined or sequential estradiol hemihydrate and norethisterone. RESULTS: Of the 447 women randomly assigned, 442 could be followed for a median of 4 years. Thirty-nine of the 221 women in the HT arm and 17 of the 221 women in the control arm experienced a new breast cancer event (HR = 2.4, 95% CI = 1.3 to 4.2). Cumulative incidences at 5 years were 22.2% in the HT arm and 8.0% in the control arm. By the end of follow-up, six women in the HT arm had died of breast cancer and six were alive with distant metastases. In the control arm, five women had died of breast cancer and four had metastatic breast cancer (P = .51, log-rank test). CONCLUSION: After extended follow-up, there was a clinically and statistically significant increased risk of a new breast cancer event in survivors who took HT. 2007 Review-absence of safety data- Antoine- Belgium humrep.oxfordjournals.org/content/22/2/616.long www.ncbi.nlm.nih.gov/pubmed/17050551 Hum Reprod. 2007 Feb;22(2):616-22. Epub 2006 Oct 18. Safety of hormone therapy after breast cancer: a qualitative systematic review. Antoine C, Liebens F, Carly B, Pastijn A, Neusy S, Rozenberg S. Department of Obstetrics and Gynaecology, Free Universities of Brussels , Belgium. This qualitative review systematically analyses the safety of hormone therapy (HT) in breast cancer (BC) patients. METHODS: We systematically searched studies reporting the use of HT in BC patients. We selected 20 studies in which we evaluated the methodology, characteristics of the studied populations and outcomes in terms of mortality and recurrence rates (RRs). RESULTS:Many studies evaluating HT were uncontrolled and retrospective. Ten prospective and two randomized studies were found. These were characterized by heterogeneity in populations, tumour characteristics, prognostic factors and treatments. Two studies reported a reduced RR, and two reported lowered BC mortality rates in HT users. One randomized study reported an increased rate of new BC events in HT users. CONCLUSIONS: There are currently no reassuring data indicating the absence of a harmful effect of HT. Further studies should analyse whether some regimens are safer than others. There is a need for randomized trials assessing the safety of these regimens. In the meantime, patients should be informed about the absence of safety data. ---------------------------------------------------------------- 2007 Observational Study Germany - 1072 patients Better prognosis for those who used HRT before cancer diagnosis http://www.ncbi.nlm.nih.gov/pubmed/17403414 Am J Obstet Gynecol. 2007 Apr;196(4):342.e1-9. Reduced incidence of distant metastases and lower mortality in 1072 patients with breast cancer with a history of hormone replacement therapy. Schuetz F, Diel IJ, Pueschel M, von Holst T, Solomayer EF, Lange S, Sinn P, Bastert G, Sohn C. Breast Unit, University Hospital Heidelberg, Heidelberg, Germany. OBJECTIVE: Substitution of estrogens (hormone replacement therapy [HRT]) is the most common therapy and prophylaxis of postmenopausal complaints. However, in most studies, long-term HRT has been associated with an increased risk for breast cancer, but the influence on a prognosis of breast cancer has been examined rarely. STUDY DESIGN: For further investigation, we analyzed 1072 patients aged 45-70 years at the time of first diagnosis of breast cancer with and without preoperative HRT with regard to the incidence of distant metastases and overall survival. Of these, 279 women were premenopausal (mean, 47.8 +/- 3.2 years); 793 women were postmenopausal (mean, 54.5 +/- 3.5 years); 320 women had received HRT over a minimum of 1 year (mean, 5.5 +/- 4.0 years; group HRT+); and 473 women had not received HRT (group HRT-). The median follow-up time was 73.2 months. RESULTS: Although body mass index, tumor size, and grading of group HRT were significantly higher than in group HRT+, nodal status, S-phase fraction, hormone-receptor status, and local recurrence showed no significant differences. In regard to the incidence of distant metastases, women without HRT have significantly (P < .001) more metastases to bone (68 vs 20 women), lung (47:13 women), and liver (47:13 women). Overall survival was significantly lower in the HRT- group. CONCLUSION: We were able to show that the use of HRT before the diagnosis of breast cancer results in more favorable primary tumors, with a lower incidence of recurrences and a better overall survival rate. This might be due to normalized bone metabolism by the use of HRT, which may lower the conditions of tumor cell seeding. 2006-BRCA survivors request HRT for QOL www.ncbi.nlm.nih.gov/pubmed/16144734 Eur J Obstet Gynecol Reprod Biol. 2006 Feb 1;124(2):250-3. Epub 2005 Sep 6. The thoughts of breast cancer survivors regarding the need for starting hormone replacement therapy. Trinh XB, Peeters F, Tjalma WA. Department of Gynaecology and Gynaecologic Oncology, University Hospital Antwerp, Edegem, Belgium. Abstract There is not only a need for scientific data regarding the risk of recurrence of breast cancer by starting hormone replacement therapy (HRT) but also regarding the patients' needs for HRT. OBJECTIVES:To examine the severity of climacteric complaints in breast cancer patients and to examine if they are willing to take HRT. METHODS:In November 2003, a questionnaire was sent to 469 breast cancer survivors. The survey examined on a scale base the severity of climacteric complaints and the patient's opinion on starting HRT. RESULTS:More than 76% of the patients complained that they experience or had experienced hot flushes or night sweating. More than half (53%) of this group found the inconvenience severe to extreme, affecting the patient's quality of life. A majority (80.5%) patients who had already taken HRT, found that it improved their quality of life substantially. When the results of observational studies were explained regarding HRT in breast cancer survivors, a majority said they would take or would consider taking HRT (57.9%). CONCLUSION:While physicians are more reserved in prescribing HRT in breast cancer survivors, a combination of severe symptomatic climacteric complaints and the willingness of the patient to be treated should at least result in a "consideration" of prescribing HRT. -------------------------------------------------------------------------------- www.ncbi.nlm.nih.gov/pmc/articles/PMC1175078/?tool=pubmed www.ncbi.nlm.nih.gov/pmc/articles/PMC1175078/ Breast Cancer Res. 2005; 7(4): 168–170. Menopausal hormone therapy after breast cancer Graham A Colditz ----------------------------------------- 2004 Israel Guidelines Changed Because of HABIT -NO Longer Recommended www.ncbi.nlm.nih.gov/pubmed/15521355 Harefuah. 2004 Oct;143(10):753-6, 764. [Hormone replacement therapy in breast cancer survivors: the Israeli Society for Clinical Oncology and Radiotherapy policy letter]. [Article in Hebrew] Siegelmann-Danieli N, Ron I, Kaufman B, Uzieli B, Karminsky N, Inbar M; Israeli Society for Clinical Oncology and Radiotherapy. Geisinger Medical Center, Danville, PA, USA. The Israeli Society for Clinical Oncology and Radiotherapy appointed experts in breast cancer therapy to assess the Society's policy regarding hormone replacement therapy (HRT) in breast cancer survivors with menopausal symptoms. The first policy letter was published in November 2002, and referred to available literature at that time which included retrospective data alone. The professional literature suggested no increased risk in breast cancer recurrence or cancer specific mortality, and no effect on overall survival with the use of HRT for a limited period (up to 3 years). This data served as the rationale for international prospective studies. Former committee recommendations and precautions are detailed in the original publication. In February 2004, the interim analysis of a prospective trial, the HABIT (Hormonal replacement therapy after breast cancer--is it safe?) was published. In that trial, breast cancer survivors with menopausal symptoms were randomized to HRT (estrogens with or without progestins) or no therapy for 2 years. A total of 434 women were recruited from centers in Scandinavia who participated with the International Breast Cancer and the European Organization for Research and Treatment groups. Analysis was restricted to 345 women with at least one follow up report; median follow-up period was 2.1 years. The relative risk for breast cancer event was 3.5 (95% C.I. 1.5-8.1) in HRT users as compared with the non-HRT group and the HABIT trial was terminated. Study limitations are discussed. Thereby, at this time HRT can no longer be considered safe in breast cancer survivors. Physicians treating breast cancer survivors for severe menopausal symptoms should present study results and alternative non-hormonal treatment options to allow patients optimized consented treatment decisions. 2004 Canada OB Gyne Guidelines www.sogc.org/guidelines/public/142E-CPG-January2004.pdf USE OF HORMONAL REPLACEMENT THERAPY AFTER TREATMENT OF BREAST CANCER This guideline has been reviewed by the Breast Disease Committee and approved by the Executive and Council of the Society of Obstetricians and Gynaecologists of Canada. CONCLUSIONS The opinion that estrogens and estrogen treatment are deleterious for breast cancer needs to be refocused. Knowing the current data, a proper risk-benefit assessment of HRT use in women with risk factors for breast cancer or in women diagnosed with a breast cancer needs to be presented. We need to wait for the prospective, randomized clinical trials that are presently ongoing to have a definitive conclusion. RECOMMENDATIONS 1. HRT after treatment of breast cancer has not been demonstrated to have an adverse impact on recurrence and mortality. (II-2 2. HRT is an option in postmenopausal women with previously treated breast cancer. (II-2 3. Prospective, randomized clinical trial results are needed. (III-A) 2003 - Observational Study 230 patients France-same relapse rate as case controls http://www.ncbi.nlm.nih.gov/pubmed/14563605 Gynecol Obstet Fertil. 2003 Jul-Aug;31(7-8):614-9. [Hormone replacement therapy in breast cancer patients: a study of 230 patients, with a case- control study] [Article in French] Gorins A, Espie M, Bedairia N, Perret F, Tournant B, Novak H, Lucchi-Angelier E, Marty M. Centre des maladies du sein, hopital Saint-Louis, 1, avenue Claude-Vellefaux, 7574, Paris, France. OBJECTIVES: After recalling the classical contra-indication of hormone replacement therapy (HRT) concerning patients with a personal history of breast cancer (BC), and arguments that may be opposed, the authors report the present results of a prospective study undertaken in the Center of Breast Diseases in Saint-Louis hospital in Paris since February 1992. PATIENTS AND METHODS: By April 2001, 230 patients had been included. A free interval of 2 years at least since the treatment of the primary BC has been observed. The reasons for prescribing HRT were vasomotor troubles (flushes, nightly sweats) or a dyspareunia, which were severe and not controlled by non-hormonal treatments. There was also an indication of a major osteoporotic or cardiovascular danger. In fact, many of these patients had a premature, artificial, chemo-induced menopause. The HRT most often used was an estro-progestin association (estradiol + a progestin compound) given either continuously or with a 5-d interruption each month. The mean duration of treatment was 2.5 years. RESULTS: Results, concerning the improvement of menopause troubles, were remarkable in the great majority of troubles. HRT had to be stopped in 39 cases, reading as follows: 17 cases for relapses (seven local, six in the contro-lateral breast and four metastases (7%)). Also, 22 patients (9%) interrupted their HRT for serious side-effects. A case-control study did not show any significant difference between with and without HRT patients concerning the overall survival without relapse. DISCUSSION AND CONCLUSIONS: Quality of life of patients was often substantially improved, and a deleterious effect on the cancer disease was not found. Our results are in agreement with the literature from other countries. However, one must be cautious. In such circumstances, HRT must be prescribed with the informed consent of the patients and delivered in appropriate hospital and university centers. It is wished that large randomised prospective studies may be undertaken. 2002 Pritchard- Canada- HRT recommendation in Breast Cancer Survivors www.ncbi.nlm.nih.gov/pubmed/17308160 CMAJ. 2002 April 16; 166(8): 1017–1022. Clinical practice guidelines for the care and treatment of breast cancer: 14. The role of hormone replacement therapy in women with a previous diagnosis of breast cancer. Kathleen I. Pritchard, Humaira Khan, Mark Levine, and The Steering Committee on Clinical Practice Guidelines for the Care and Treatment of Breast Cancer To provide information and recommendations to women with a previous diagnosis of breast cancer and their physicians regarding hormone replacement therapy (HRT). Outcomes Control of menopausal symptoms, quality of life, prevention of osteoporosis, prevention of cardiovascular disease, risk of recurrence of breast cancer, risk of death from breast cancer. Evidence Systematic review of English-language literature published from January 1990 to July 2001 retrieved from MEDLINE and CANCERLIT. Recommendations Routine use of HRT (either estrogen alone or estrogen plus progesterone) is not recommended for women who have had breast cancer. Randomized controlled trials are required to guide recommendations for this group of women. Women who have had breast cancer are at risk of recurrence and contralateral breast cancer. The potential effect of HRT on these outcomes in women with breast cancer has not been determined in methodologically sound studies. However, in animal and in vitro studies, the development and growth of breast cancer is known to be estrogen dependent. Given the demonstrated increased risk of breast cancer associated with HRT in women without a diagnosis of breast cancer, it is possible that the risk of recurrence and contralateral breast cancer associated with HRT in women with breast cancer could be of a similar magnitude. · Postmenopausal women with a previous diagnosis of breast cancer who request HRT should be encouraged to consider alternatives to HRT. If menopausal symptoms are particularly troublesome and do not respond to alternative approaches, a well-informed woman may choose to use HRT to control these symptoms after discussing the risks with her physician. In these circumstances, both the dose and the duration of treatment should be minimized. theoncologist.alphamedpress.org/content/6/4/353.full Oncologist. 2001;6(4):353-62. Hormone replacement in women with a history of breast cancer. Pritchard KI.Toronto-Sunnybrook Regional Cancer Centre and The University of Toronto, Toronto, Ontario, Canada. kathy.pritchard@tsrcc.on.ca ------------------------------------------- =============================== www.breastcancerchoices.org/files/ImprovedSurvon_HRT.pdf The American Society of Breast Surgeons - Improved breast cancer survival among hormone replacement therapy users is durable after 5 years of additional follow-up Dara Christante, M.D., SuEllen Pommier, Ph.D., Jennifer Garreau, M.D., Patrick Muller, B.S., Brett LaFleur, B.S., Rodney Pommier, M.D.* Division of Surgical Oncology, Department of Surgery, Portland, OR, USA '''''''''''''''''' 2001 J Nat Cancer Inst O'Meara Free Full Text: http://jnci.oxfordjournals.org/content/93/10/754.long http://www.ncbi.nlm.nih.gov/pubmed/11353785 J Natl Cancer Inst. 2001 May 16;93(10):754-62. Hormone replacement therapy after a diagnosis of breast cancer in relation to recurrence and mortality. O'Meara ES, Rossing MA, Daling JR, Elmore JG, Barlow WE, Weiss NS. Source Fred Hutchinson Cancer Research Center and Department of Epidemiology, University of Washington, Seattle, USA. Hormone replacement therapy (HRT) is typically avoided for women with a history of breast cancer because of concerns that estrogen will stimulate recurrence. In this study, we sought to evaluate the impact of HRT on recurrence and mortality after a diagnosis of breast cancer. METHODS: Data were assembled from 2755 women aged 35-74 years who were diagnosed with incident invasive breast cancer while they were enrolled in a large health maintenance organization from 1977 through 1994. Pharmacy data identified 174 users of HRT after diagnosis. Each HRT user was matched to four randomly selected nonusers of HRT with similar age, disease stage, and year of diagnosis. Women in the analysis were recurrence free at HRT initiation or the equivalent time since diagnosis. Rates of recurrence and death through 1996 were calculated. Adjusted relative risks were estimated by use of the Cox regression model. All statistical tests were two-sided. RESULTS: The rate of breast cancer recurrence was 17 per 1000 person-years in women who used HRT after diagnosis and 30 per 1000 person-years in nonusers (adjusted relative risk for users compared with nonusers = 0.50; 95% confidence interval [CI] = 0.30 to 0.85). Breast cancer mortality rates were five per 1000 person-years in HRT users and 15 per 1000 person-years in nonusers (adjusted relative risk = 0.34; 95% CI = 0.13 to 0.91). Total mortality rates were 16 per 1000 person-years in HRT users and 30 per 1000 person-years in nonusers (adjusted relative risk = 0.48; 95% CI = 0.29 to 0.78). The relatively low rates of recurrence and death were observed in women who used any type of HRT (oral only = 41% of HRT users; vaginal only = 43%; both oral and vaginal = 16%). No trend toward lower relative risks was observed with increased dose. CONCLUSION: We observed lower risks of recurrence and mortality in women who used HRT after breast cancer diagnosis than in women who did not. Although residual confounding may exist, the results suggest that HRT after breast cancer has no adverse impact on recurrence and mortality. Unopposed estrogens only - 50% less recurrence compared to never users. www.menopausemgmt.com/issues/10-04/News%20Briefs.pdf O’Meara ES, Rossing MA, Daling JR, et al. J Natl Cancer Inst 2001;93:754-61) Hormone replacement therapy after a diagnosis of breast cancer in relation to recurrence and mortality. HRT After Breast Cancer: Recurrence and Mortality Findings from a data analysis suggest that hormone replacement therapy (HRT) in women previously diagnosed with invasive breast cancer does not appear to increase the risk of recurrence or mortality, and might even have a protective effect. --------------------------------------------------------- 2001 Review of the Literature 4.2% recurrence for HRT users, 5.4 % recurrence for non-HRT users jco.ascopubs.org/content/19/8/2357.abstract J Clin Oncol. 2001 Apr 15;19(8):2357-63. Hormone replacement therapy after breast cancer: a systematic review and quantitative assessment of risk. Col NF, Hirota LK, Orr RK, Erban JK, Wong JB, Lau J. Division of General Medicine and Decision Systems Group, Brigham and Women's Hospital and Harvard Medical School, Chestnut Hill, MA 02467, USA. PURPOSE: Hormone replacement therapy (HRT) is typically withheld from women with breast cancer because of concern that it might increase the risk of recurrence. The purpose of this study was to quantify the risk of recurrent breast cancer associated with HRT among breast cancer survivors. METHODS: We performed a systematic literature review through May 1999, calculating the relative risk (RR) of breast cancer recurrence in each study by comparing the number of recurrences in the HRT group to those in the control group. In studies that did not contain a control group, we constructed one by estimating the expected number of recurrences based on data from the Early Breast Cancer Trialists' Collaborative Group, adjusting for nodal status and disease-free interval. RRs across all studies were combined using random-effects models. RESULTS: Of the 11 eligible studies, four had control groups and included 214 breast cancer survivors who began HRT after a mean disease-free interval of 52 months. Over a mean follow-up of 30 months, 17 of 214 HRT users experienced recurrence (4.2% per year), compared with 66 of 623 controls (5.4% per year). HRT did not seem to affect breast cancer recurrence risk (RR = 0.64, 95% confidence interval [CI], 0.36 to 1.15). Including all 11 studies in the analyses (669 HRT users), using estimated control groups for the seven uncontrolled trials, the combined RR was 0.82 (95% CI, 0.58 to 1.15). CONCLUSION: Although our analyses suggest that HRT has no significant effect on breast cancer recurrence, these findings were based on observational data subject to a variety of biases. Dr Donnica www.drdonnica.com/news/00003202.htm 5-24-01 - HRT After Breast Cancer Does Not Increase Risk Of Cancer Recurrence Or Mortality There has been lots of conflicting news about the relationship between hormone replacement therapy and breast cancer. The latest study to address this issue comes from the Journal of the National Cancer Institute (5/16/01). The study found that for women who have already had breast cancer, hormone replacement therapy did NOT increase their risk of breast cancer recurrence. In fact, the study found that HRT might even lower the chances of a breast cancer recurrence in those women and lower their risk of death from breast cancer if it does recur. In addition, this study showed that HRT use after a diagnosis of breast cancer reduced the relative risk of death from all causes. Investigators at the University of Washington in Seattle evaluated data from 2,755 women, aged 35 to 74, who had been diagnosed with invasive breast cancer between 1977 and 1994. Of these women, there were 174 who elected to use hormone replacement therapy after their diagnosis. Each of those HRT users was matched to 4 randomly selected nonusers with similar age, disease stage, and year of diagnosis. After following these women for approximately 4 years, rates of breast cancer recurrence and death from all causes was calculated. The results show that the rate of breast cancer recurrence was 17 per 1000 person-years in women who used HRT after their diagnosis of breast cancer, and nearly twice as high (30 per 1000 person-years) in women who did not use HRT after their diagnosis. Breast cancer mortality rates were 5 per 1000 person-years in HRT users and three times higher (15 per 1000 person-years) in nonusers. Mortality rates from all causes were nearly twice as high in the women who did not use HRT (16 per 1000 person-years in HRT users versus 30 per 1000 person-years in nonusers). What do these numbers mean in plain English? After following these women for nearly 4 years, investigators found that the rate of cancer recurrence in women who used HRT after having been diagnosed with invasive breast cancer was approximately HALF of what it was in nonusers after adjustment for confounding factors. When they evaluated causes of death in these women, the researchers found that the risk of death from breast cancer was three times greater in the women who did NOT use HRT than in the women who did. When death from ALL causes was evaluated, the women who did not take HRT had TWICE the risk of death compared to the women who took HRT. The results did not vary based upon the length of time that the women took HRT or whether they used the vaginal or pill form of HRT. The results of this study argue against any causal influence of HRT on breast cancer recurrence and mortality. It may also influence the recommendations that women are given about resuming HRT after breast cancer diagnosis. --------------------------------------------------------- 1999 - Informed consent- HRT may increase recurrence rate of BR CA http://jco.ascopubs.org/content/17/1/130.full.pdf http://www.ncbi.nlm.nih.gov/pubmed/10458226 Elements of Informed Consent for Hormone Replacement Therapy in Patients With Diagnosed Breast Cancer By Rowan T. Chlebowski and Anne McTiernan J Clin Oncol. 1999 Jan;17(1):130-42. University of California Los Angeles School of Medicine, Harbor-UCLA, Medical Center, Torrance 90509, USA. "HRT use is associated with not only the risk of developing a new breast cancer (the end point used in most observational studies describing breast cancer ‘‘risk’’), but also the additional and more proximate risk of stimulating growth and clinical expression of pre-existing breast cancer metastatic foci." An approach to providing informed consent to breast cancer survivors considering hormone replacement therapy (HRT) is offered. METHODS: Current information on HRT, breast cancer, and chronic disease prevention is reviewed in the context of risks faced by women with resected breast cancer. RESULTS: Breast cancer patients, unwilling to trade symptom reduction for even a small increase in recurrence risk, are at substantially increased risk of death from breast cancer relative to other causes. Observational studies suggest that long-term HRT increases breast cancer development. The influence of HRT on the growth of established breast cancer has not been determined; however, estrogen reduction (oophorectomy) significantly reduces recurrence in premenopausal women, and current evidence cannot exclude a risk that HRT increases recurrence to the same degree. The following issues are of particular relevance to breast cancer survivors: HRT reduces mammographic sensitivity, increases thromboembolic events, and increases endometrial cancer risk. Although benefit for HRT is commonly inferred from observational studies, randomized trials of HRT on all-cause mortality have not been completed. For coronary heart disease prevention, an array of strategies independent of HRT are available, with some (tamoxifen, selective estrogen receptor modifiers [SERMs], diet, and exercise) likely to favorably influence breast cancer risk; for osteoporosis prevention, an array of strategies also are available, with some (bisphosphonates, tamoxifen, SERMs, and exercise) likely to favorably influence breast cancer risk. CONCLUSION: Current data preclude the generation of evidence-based guidelines for HRT use in breast cancer survivors, and clinical trials in this setting should be supported. However, given available therapeutic alternatives for menopausal symptom management and chronic disease prevention, breast cancer survivors should be offered HRT only with caution and with their full participation in the decision-making process. ---------------------------------------------- 1999 - 21 Breast Cancer Survivors Treated with HRT -Slovenia Estradiol and Progestagens Eur J Surg Oncol. 1999 Apr;25(2):146-51. A case-control study of hormone replacement therapy after primary surgical breast cancer treatment. Ursic-Vrscaj M, Bebar S. Institute of Oncology, Department of Gynecological Oncology, Ljubljana, Slovenia. In order to make a detailed analysis, we selected a group of 21 patients with the diagnosis of invasive breast cancer who had HRT after primary surgical treatment. Each patient from the selected group was compared with two patients from the control group with the diagnosis of invasive breast cancer who did not have HRT after primary surgical treatment. The control cases were matched to selected HRT patients with regard to age at time of the diagnosis, year of diagnosis, diameter of the tumour, metastatic spread in the axillary lymph nodes, and disease-free interval until applying HRT. The same criteria were applied in all analyses. The data were analysed by odds ratio (OR) calculation with a confidence interval of 95%, taking into account residual malignancy and death due to breast cancer in both groups (including carcinoma in the contralateral breast). RESULTS: HRT was applied in 21 patients treated for breast cancer. In 33% of them, radical mastectomy revealed metastases in the axillary lymph nodes. Hormone receptors could not be found in 57% of patients. In the majority of patients the tumour measured 17.6mm in diameter. HRT was started on average 62 months (range 1-180 months) after diagnosis, and lasted an average of 28 months (range3 72 months). All 21 patients used oestradiol as HRT, i.e. a non-conjugated oestrogen. Combined hormonal therapy (oestrogens + progestagens) was given to 95% of patients with median age of 47 years (range 41-59 years) at the beginning of HRT. Relapse was observed in four patients (19%) of the HRT group; of these, one had a carcinoma of the contralateral breast. In the control group, relapse was observed in five patients (11%); one of these five patients had a carcinoma of the contralateral breast. In the HRT group, there were no deaths among the patients with confirmed relapse, while one patient died in the control group. The estimated risk (OR= 1.74, 95%S CI 0.34-8.88) of relapse of breast cancer was calculated by comparing data from HRT users, who had received HRT for 28 months (range 3-72 months) on average, with data from the control group. The estimated risk of breast cancer relapse in HRT users who had been receiving HRT for less than 24 months was 0.65 (OR = 0.65, 95% CI 0.02-7.85). CONCLUSION: Despite the inherent limitations of retrospective data and the need for prospective randomized trials to assess the possible influence of HRT on progression after breast cancer treatment, the present observations suggest that HRT treatment for less than 24 months does not appear to have a pronounced adverse effect on cancer outcome. Nevertheless, until appropriate clinical trials determine that HRT is safe, caution is needed. ------------------------------------------ 1998 Observational study- No increase in breast cancer recurrence after HRT oral or transdermal estrogen and a progestin www.ncbi.nlm.nih.gov/pubmed/11907916 Climacteric. 1998 Jun;1(2):137-42. A cohort study of hormone replacement therapy given to women previously treated for breast cancer. by Dew J, Eden J, Beller E, Magarey C, Schwartz P, Crea P, Wren B. Women's Health Institute, Royal Hospital for Women, Barker Street, Randwick, NSW 2031, Australia. Women who have been previously treated for breast cancer are usually advised to avoid hormone therapy for fear of increasing their risk of tumor recurrence. However, for some women, menopausal symptoms are so severe that their quality of life is poor. Because ethic committees are reticent to permit a double-blind randomized trial, we performed a cohort study of hormone therapy after breast cancer. METHODS: The study group comprised 1472 women with breast cancer. A total of 167 subjects had used an oral or transdermal estrogen after their treatment for breast cancer. Amongst these estrogen users, 152 (91%) had also used a progestin. In total, 106 other women had used a progestin alone as a treatment for menopausal flushes and not as a treatment for breast cancer. Cox regression analysis was performed using estrogen as a time-dependent covariate with disease-free interval as the outcome. RESULTS: The uncorrected hazard ratio for the estrogen-progestin users was 0.67 (95% confidence interval (CI) 0.38-1.16) and for the progestin alone users was 0.85 (95% CI 0.44-1.65). CONCLUSIONS: This study was unable to demonstrate a significant increase in risk of breast cancer recurrence for women who used HRT and suggests that the time is now appropriate for a randomized prospective trial of hormone therapy after breast cancer. ------------------------------------------------------------------------- 1996 www.moffitt.org/CCJRoot/v3n2/article1.html Cancer Control Journal Vol 3, No. 2 March/April 1996 Hormone Replacement Therapy in the Gynecologic and Breast Cancer Patient Philip J. DiSaia, MD ======================================== 1993 Am J Surg. 1993 Mar;165(3):372-5. Hormone replacement therapy in previously treated breast cancer patients. Wile AG, Opfell RW, Margileth DA. Department of Surgery, UC Irvine 92668. We report our experience with 25 women previously treated for breast cancer who subsequently received hormone replacement therapy (HRT) for the relief of menopausal symptoms and the prevention of postmenopausal cardiovascular disease and osteoporosis. Two patients had in situ disease, 13 had stage I disease, 7 had stage II disease, 1 had stage III disease, and 2 had invasive cancer of undetermined stage. Seventeen patients (group I) began HRT less than 24 months after primary breast cancer therapy, and 8 patients (group II) began HRT more than 24 months after breast cancer therapy. The HRT-free interval for group I patients averaged 7.9 months and for group II patients averaged 64.5 months. The average period of observation while receiving HRT for the entire group was 35.2 months (range: 24 to 82 months). Three of 25 patients have had a recurrence, all in group I. One patient developed local recurrence after breast conservation treatment, and her condition was salvaged by further wide excision. Two patients developed recurrence after mastectomy, and one patient ultimately died of systemic disease. The overall survival rate for the entire group was 96%. Overall survival of high-risk group I patients, with a mean follow-up of 30.4 months, was 94%. We recognize that this report of HRT in a small group of patients does not have the power to demonstrate an adverse effect of HRT on breast cancer. However, the lack of an obvious adverse effect of HRT in this group of breast cancer patients and the known beneficial effect of HRT on postmenopausal cardiovascular disease and osteoporosis warrant formal prospective trials of HRT in such patients. ----------------------------------------------- 2009 survey among OB GYNEs - Greece www.ncbi.nlm.nih.gov/pubmed/19317264 Eur J Gynaecol Oncol. 2009;30(1):82-4. Hormone therapy for postmenopausal breast cancer survivors: a survey among obstetrician-gynaecologists. Vavilis D, Zafrakas M, Goulis DG, Pantazis K, Agorastos T, Bontis JN. Source Department of Obstetrics and Gynaecology, Papageorgiou Hospital, Aristotle University of Thessaloniki, Greece. To investigate the attitude of Greek obstetrician-gynaecologists towards prescription of hormone therapy to postmenopausal breast cancer survivors. METHODS:An anonymous questionnaire was sent to members of the Hellenic Society of Obstetrics and Gynaecology with a hypothetical case and a series of relevant questions. RESULTS:Three hundred valid answers were received. Hormone therapy would be prescribed to a breast cancer survivor by only 8%; 80% of these would prefer tibolone. In contrast, 92% would not prescribe hormone therapy; 97% would do so due to the risk of disease recurrence; 70% would not prescribe any alternative therapy, 21% would prescribe CNS-active compounds and 7% SERMs. CONCLUSIONS:The vast majority of Greek obstetrician-gynaecologists would not prescribe hormone therapy for menopausal symptoms in breast cancer survivors due to the theoretical risk of disease recurrence. Among those who would not prescribe hormone therapy, 21% would opt to CNS-active compounds. 2006 www.ncbi.nlm.nih.gov/pubmed/16143444 Eur J Obstet Gynecol Reprod Biol. 2006 Feb 1;124(2):207-11. Epub 2005 Sep 6. The thoughts of physicians regarding the need to start hormone replacement therapy in breast cancer survivors. Trinh XB, Van Hal G, Weyler J, Tjalma WA. Department of Gynaecology and Gynaecologic Oncology, University Hospital Antwerp, Wilrijkstraat 10, 2650 Edegem, Belgium. To investigate how physicians felt about HRT use in breast cancer survivors a half year after the WHI trial. METHODS:In December 2002, a questionnaire was conducted in Flanders (Belgium). The survey contained a presentation of a 35-year-old breast cancer survivor who presented with climacteric symptoms after treatment with tamoxifen. RESULTS:With a response rate of 33.65%, a majority of the physicians did not prescribe classical oral HRT (5.40%) in this patient. Physicians prefer to prescribe tibolone (30.68%) or other alternative treatment (50.00%). The main reason was the fear for increased recurrence of breast cancer. Furthermore the WHI oestrogen plus progestin trial and its attention in the media, a half year prior to the survey, influenced one-third of the physician's prescribing attitude. CONCLUSIONS:Two-thirds of the physicians did not change prescribing attitude after the WHI oestrogen plus progestin trial. HRT is a well proven effective treatment in breast cancer survivors with severe climacteric complaints, but a majority of physicians is not convinced of its safety in breast cancer survivors. Therefore, a majority of physicians do not find the need to prescribe HRT in breast cancer survivors. ================================================= www.ncbi.nlm.nih.gov/pubmed/21278517 Clin Obstet Gynecol. 2011 Mar;54(1):173-9. Hormone replacement after breast cancer: is it safe? Liotta M, Escobar PF.Division of Gynecologic Oncology, Department of Obstetrics and Gynecology, The Cleveland Clinic, Cleveland, Ohio, USA. The use of hormone therapy for climacteric symptoms in patients with breast cancer has become a significant and important point of discussion due in part to the improved survival from this disease in recent years. There is a theoretic risk that exogenous hormones will stimulate the growth of microscopic disease and lead to decreased survival and increased recurrence. In addition, 2 large studies have shown that there is an association between hormone therapy and breast cancer risk in women without an earlier history of breast cancer. Other studies suggest that estrogen alone may have a superior safety profile than estrogen and progesterone in combination. Hormone therapy could be justified for improvement of quality of life when other options have failed and the patient is informed of the risks. 2011 HRT in Premature Menopause www.ncbi.nlm.nih.gov/pubmed/21561765 Eur J Cancer. 2011 Jul;47(11):1623-32. Epub 2011 May 9. Hormone replacement therapy and women with premature menopause--a cancer survivorship issue. King J, Wynne CH, Assersohn L, Jones A. Oncology Department, Royal Free Hampstead NHS Trust, Pond Street, London NW3 2PF, United Kingdom. judyking@doctors.org.uk Abstract The importance of addressing survivorship issues has been emphasised in recent years. As cancer therapies improve there is a growing population of cancer survivors, which includes many women with premature menopause. Women who are premenopausal at the time of their cancer diagnosis may have specific survivorship issues to be addressed, including infertility, early menopause and sexual dysfunction. These factors can continue have a significant impact on the quality of life of these patients at long term follow up. Data for this Review were identified by searches of MEDLINE, PubMed, and references from relevant articles using the search terms 'HRT', 'women/female cancer/tumour', 'menopause' and 'survivorship'. Abstracts and reports from meetings were excluded. Only papers published in English between 1980 and 2010 were included. The aims of this review are to: • Address the hormonal factors which impact on cancer survivorship for premenopausal women • Review the debate for the role of hormone replacement therapy (HRT) in cancer survivors • Provide information for physicians and patients regarding the management of hormonally driven survivorship issues (for different tumour types), based on current evidence The recommendations for practice are that HRT may be offered for the alleviation of vasomotor symptoms in cancer survivors who undergo premature menopause up to the age of natural menopause (51 years in the UK). HRT (including vaginal oestrogen preparations) is contraindicated in survivors of oestrogen receptor positive breast cancer and low grade endometrial leiomyosarcoma, where non-HRT alternatives should be considered to alleviate symptoms. Oncologist. 2001;6(4):353-62. Hormone replacement in women with a history of breast cancer. Pritchard KI. Source Toronto-Sunnybrook Regional Cancer Centre and The University of Toronto, Toronto, Ontario, Canada. kathy.pritchard@tsrcc.on.ca ________________________________________ 2000 DiSaia Am J Clin Oncol. 2000 Dec;23(6):541-5. Breast cancer survival and hormone replacement therapy: a cohort analysis. DiSaia PJ, Brewster WR, Ziogas A, Anton-Culver H. Department of Obstetrics and Gynecology, University of California Irvine Medical Center, The Chao Family Comprehensive Cancer Center, 92868, USA. Controversy exists regarding the safety of hormone replacement therapy (HRT) after a diagnosis of breast cancer. The objective of this study is to perform a matched cohort analysis to evaluate the impact of HRT on mortality in breast cancer survivors. Patients with breast cancer who received HRT after diagnosis of breast cancer were identified. Control subjects were identified from the regional cancer registry. Matching criteria included age at diagnosis, stage of breast cancer, and year of diagnosis. Controls were selected only if they were alive at the time of initiation of HRT of the matched case. Only subjects not included in a previously reported matched analysis were selected. One hundred twenty-five cases were matched with 362 controls. Ninety-eight percent (123/125) of the cases received systemic estrogen; 90/125 (72%) also received a progestational agent. The median interval between diagnosis of breast cancer and initiation of HRT was 46 months (range 0-401 months). The median duration of HRT was 22 months (range 1-357 months). The risk of death was lower among the HRT survivors; odds ratio 0.28 (95% confidence interval 0.11-0.71). This analysis does not suggest that HRT after the treatment of breast cancer is associated with an adverse outcome. _____________________________ ___________________________ Oncology. 2001;60(3):199-206. Hormone replacement therapy after treatment of breast cancer: effects on postmenopausal symptoms, bone mineral density and recurrence rates. Beckmann MW, Jap D, Djahansouzi S, Nestle-Kramling C, Kuschel B, Dall P, Brumm C, Bender HG. Department of Obstetrics and Gynecology, Friedrich Alexander University, Erlangen, Germany. PURPOSE: Breast cancer (BC) is the most frequent female carcinoma and the major cause of death in women aged 35--50 years. The total number of patients surviving BC and especially the morbidity rate of patients below the age of 55 years has increased significantly in the last several years. As a consequence, the number of BC patients suffering from the long-term effects of estrogen deficiency due to adjuvant treatment is increasing. At present, hormone replacement therapy (HRT) following BC treatment is applied individually and mainly depends on the severity of postmenopausal symptoms (PMS) experienced by these patients. PATIENTS AND METHODS: In a retrospective study (total n = 185 BC patients, 64 with and 121 without HRT), the effect of HRT during or after adjuvant therapy [chemotherapy and/ or (anti-) hormonotherapy] has been investigated. The surveillance period was up to 60 months. Evaluated were HRT effects on (1) PMS measured by a comprehensive life quality questionnaire, (2) bone mineral density (BMD) measured by osteodensitometry and (3) morbidity as well as mortality rates. RESULTS: Both groups did not differ with regard to tumor stage, lymph node involvement, metastasis, grading, and steroid hormone receptor status. A reduction in PMS was significant in women taking HRT (p < 0.001), especially in the subgroup of women < or =50 years (p < 0.0001). For both age groups, the median reduction in BMD (z-score) was less in women receiving HRT (< or =50 years: without HRT -1.99 vs. with HRT -0.95, p < 0.05; >50 years: without HRT -2.29 vs. with HRT -1.19, p < 0.01). There were no statistically significant differences regarding morbidity and mortality (p = 0.29). CONCLUSION: In this study of BC patients, the use of HRT shows positive effects on PMS and BMD. There was no significant influence on morbidity or mortality. However, a reevaluation of HRT in the routine management of BC patients should await the results of prospective randomized trials. Copyright 2001 S. Karger AG, Basel ___________________________ J Clin Oncol. 1999 May;17(5):1482-7. Estrogen replacement therapy after localized breast cancer: clinical outcome of 319 women followed prospectively. Vassilopoulou-Sellin R, Asmar L, Hortobagyi GN, Klein MJ, McNeese M, Singletary SE, Theriault RL. Department of Breast and Gynecologic Medical Oncology, M.D. Anderson Cancer Center, University of Texas, Houston 77030, USA. PURPOSE: To determine whether estrogen replacement therapy (ERT) alters the development of new or recurrent breast cancer in women previously treated for localized breast cancer. PATIENTS AND METHODS: Potential participants (n = 319) in a trial of ERT after breast cancer were observed prospectively for at least 2 years whether they enrolled onto the randomized trial or not. Of 319 women, 39 were given estrogen and 280 were not given hormones. Tumor size, number of lymph nodes, estrogen receptors, menopausal status at diagnosis, and disease-free interval at the initiation of the observation period were comparable for the trial participants (n = 62) versus nonparticipants (n = 257) and for women on ERT (n = 39) versus controls (n = 280). Cancer events were ascertained for both groups. RESULTS: Patient and disease characteristics were comparable for the trial participants versus nonparticipants, as well as for the women on ERT versus the controls. One patient in the ERT group developed a new lobular estrogen receptor-positive breast cancer 72 months after the diagnosis of a ductal estrogen receptor-negative breast cancer and 27 months after initiation of ERT. In the control group, there were 20 cancer events: 14 patients developed new or recurrent breast cancer at a median time of 139.5 months after diagnosis and six patients developed other cancers at a median time of 122 months. CONCLUSION: ERT does not seem to increase breast cancer events in this subset of patients previously treated for localized breast cancer. Results of randomized trials are needed before any changes in current standards of care can be proposed. ___________________________ Am J Obstet Gynecol. 1996 May;174(5):1494-8. Hormone replacement therapy in breast cancer survivors: a cohort study. DiSaia PJ, Grosen EA, Kurosaki T, Gildea M, Cowan B, Anton-Culver H. Department of Obstetrics and Gynecology, University of California, Irvine Medical Center, Orange, CA 92668, USA. OBJECTIVE: Our purpose was to measure any adverse effect (if one exists) of hormone replacement therapy administered to breast cancer survivors. STUDY DESIGN: Forty-one patients from a group of 77 patients who received hormone replacement therapy after therapy for breast cancer were matched with 82 comparison patients not receiving hormone replacement therapy. Both groups were taken from the same population on the basis of cancer registry of the Cancer Surveillance Program of Orange County and were compared with regard to survival results. RESULTS: An analysis of survival time and disease-free time revealed no statistically significant difference between the two groups. CONCLUSIONS: No obvious adverse effect of hormone replacement therapy could be shown in this pilot study. A case is made for a prospective randomized trial. __________________________ ___________________________ Am J Obstet Gynecol. 2002 Aug;187(2):289-94; discussion 294-5. Estrogen replacement therapy in patients with early breast cancer . Natrajan PK, Gambrell RD Jr. Reproductive Endocrinologists, Augusta, GA 30910, USA. OBJECTIVE: Most physicians believe that estrogen replacement therapy is contraindicated once a patient is diagnosed with breast cancer. Recently, several studies have shown that estrogen replacement therapy may be safely used in patients with early breast cancer that has been treated successfully. These women can have severe menopausal symptoms and are at risk for osteoporosis. We reviewed the current status of women in our practice with breast cancer who received estrogen replacement therapy, who did not receive hormone replacement therapy, and who did not receive estrogenic hormone replacement therapy. STUDY DESIGN: The study group consisted of 123 women (mean age, 65.4 +/- 8.85 years) who were diagnosed with breast cancer in our practice, including 69 patients who received estrogen replacement therapy for < or = 32 years after diagnosis. The comparative groups were 22 women who used nonestrogenic hormones for < or = 18 years and 32 women who used no hormones for < or = 12 years. The group who did not receive estrogenic hormone replacement therapy received androgens with or without progestogens (such as megestrol acetate). Of the 63 living hormone users, 56 women are still being treated in our clinic, as are 15 of the 22 subjects who receive nonestrogenic hormone replacement therapy. Follow-up was done through the tumor registry at University Hospital; those patients whose tumor records were not current were contacted by telephone. RESULTS: There were 18 deaths in the 123 patients: 6 patients who received estrogen replacement therapy (8.69%), 2 patients who received nonestrogenic hormone replacement therapy (9.09%), and 10 patients who received no hormone replacement therapy (31.25%). Of the 18 deaths, 9 deaths were from breast cancer (mortality rate, 7.3%); 3 deaths were from lung cancer; 1 death was from endometrial cancer; 1 death was from myocardial infarction; 1 death was from renal failure; and 3 deaths were from cerebrovascular accidents. The 9 deaths from breast cancer included one patient who received nonestrogenic hormone replacement therapy (mortality rate, 4.5%), 6 patients who received no hormone replacement therapy (mortality rate, 11.3%), and 2 patients who received estrogen replacement therapy (mortality rate, 4.28%). The 9 non- breast cancer deaths included 4 patients who received estrogen replacement therapy (endometrial cancer [1 death], lung cancer [1 death], cerebrovascular accident [1 death], and renal failure [1 death]), 1 patient who did not receive estrogenic hormone replacement therapy group (myocardial infarction), and 4 patients who used no hormones (lung cancer, 2 deaths; stroke, 2 deaths). Carcinoma developed in one patient in the estrogen replacement therapy group in the contralateral breast after 4 years of hormone replacement therapy; she is living and well 2.5 years later with no evidence of disease. Metastatic breast cancer developed in one patient after 8 years of hormone replacement therapy; she is living with disease. CONCLUSION: Estrogen replacement therapy apparently does not increase either the risk of recurrence or of death in patients with early breast cancer. These patients may be offered estrogen replacement therapy after a full explanation of the benefits, risks, and controversies. ___________________________ Rev Med Liege. 2003 Feb;58(2):77-82. Hormone replacement therapy after breast cancer. Yes...or no? [Article in French] Foidart JM, Desreux J, Lifrange E, Colin C. Departement de Gynecologie-Obstetrique-Senologie, CHU de Liege. Clinical and experimental studies indicate that combined unique conjugated estrogens and medroxyprogesterone acetate moderately increase the risk of breast cancer in postmenopausal women. Classically, hormone replacement therapy is contra-indicated in women with a past history of breast cancer due to the fear of recurrence. However, these postmenopausal patients complain about hot flushes and adjuvant hormonal therapies (such as aromatase inhibitors, SERMs and Tamoxifen...) aggravate their symptoms. "Observational studies and their meta-analyses do not show a deleterious effect but rather a beneficial impact of hormone replacement therapy among women with a past history of breast cancer." We summarise all these studies and their biological, clinical and epidemiological interpretations. We conclude that short term hormone replacement therapy is safe among those women requesting a replacement therapy after complete information. It is however advisable to conclude definitely only when prospective randomised trials with estradiol or tibolone (a promising alternative) will be available. Such ongoing studies will allow to conclude definitely the possible benefits and risks of hormone replacement therapy among patients with a past history of breast cancer. __________________________ Int J Gynaecol Obstet. 1999 Jan;64(1):59-63. Estrogen replacement therapy in breast cancer survivors. Guidozzi F. Department of Obstetrics and Gynaecology, Johannesburg Hospital, University of the Witwatersrand Medical School, South Africa. OBJECTIVE: To determine whether estrogen replacement therapy (ERT) adversely affected outcome of breast cancer survivors. METHOD: A prospective descriptive study of all breast cancer survivors who requested ERT because of intractable menopausal symptoms. All patients presented voluntarily as gynecological outpatients and were all given oral continuous opposed ERT: 20 premarin and medroxyprogesterone and four tibolone. RESULTS: Twenty-four patients who had previously been treated for breast cancer 8-91 months prior to their initiating ERT have been observed for 24-44 months. There were 15 patients with stage 1, eight with stage 2 and one with stage 4 breast cancer. The mean age of the patients at commencement of ERT was 48 years (range 42-61). Two patients had a biopsy of a suspicious breast nodule: both of which were benign. There have not been any recurrences to date. CONCLUSION: Breast cancer survivors did not have their outcome adversely affected by ERT during an observation period of 24-44 months ------------------------- Gynecol Endocrinol. 2002 Dec;16(6):469-78. Hormone replacement therapy in women with a history of breast cancer. Ylikorkala O, Metsa-Heikkila M. Department of Obstetrics and Gynecology, Helsinki University Central Hospital, Helsinki, Finland. Health care professionals in modern Western societies will meet an increasing number of women surviving breast cancer. How the menopause of these women should be treated is still an open question. Use of hormone replacement therapy (HRT) may, at least in theory, increase the risk for recurrence of cancer, but its categoric refusal is a double-edged sword because it also denies these women all the indisputable health benefits HRT provides. This refusal is not, however, supported by the observational data available so far on this question, because HRT has not increased the risk for breast cancer recurrence. In fact, it is well established that HRT abolishes hot flushes and improves significantly these patients' quality of life. At present, we have no effective nonhormonal alternatives for the control of vasomotor symptoms, and the efficacy of phytoestrogens in the treatment of menopausal symptoms is unproven. Selective estrogen receptor modulators (SERMs) which protect against osteoporosis and perhaps also against breast cancer, and which may have beneficial effects on the cardiovascular system, aggravate hot flushes and are therefore not useful, at least in the first postmenopausal years. In some countries, progestins are often prescribed for the control of such patients' vasomotor symptoms, but their safety has never been assessed in clinical trials, and in theory they can be harmful. Randomized clinical trials (RCT) on the use of HRT in breast cancer survivors are underway, but their completion will take years, and even these may be open to criticism. Tibolone may appear to be an appealing alternative for HRT, but it should also be studied with RCTs in this indication. At present, a patient with a history of breast cancer must be given balanced information as to the possible benefits and risks of HRT, and she herself must make the decision whether or not to start HRT. Int J Fertil Womens Med. 1999 Jun-Aug;44(4):186-92. An experience with estrogen replacement therapy in breast cancer survivors. Brewster WR, DiSaia PJ, Grosen EA, McGonigle KF, Kuykendall JL, Creasman WT. Division of Gynecologic Oncology, University of California Irvine Medical Center, Orange 92868, USA. OBJECTIVE: To evaluate the outcome of breast cancer patients who elected estrogen replacement therapy (ERT). STUDY DESIGN: Breast cancer survivors who elected ERT received the preferred regimen of conjugated estrogen 0.625 mg/day with medroxyprogesterone acetate 2.5 mg/day. RESULTS: 145 patients received ERT for at least 3 months. Thirteen recurrences (9%) were identified; 10 are alive with disease, 3 are de zzzzzzzzzzzzzzzzzzzzzzzzzz Am J Obstet Gynecol. 1996 May;174(5):1494-8. Hormone replacement therapy in breast cancer survivors: a cohort study. DiSaia PJ, Grosen EA, Kurosaki T, Gildea M, Cowan B, Anton-Culver H. Department of Obstetrics and Gynecology, University of California, Irvine Medical Center, Orange, CA 92668, USA. OBJECTIVE: Our purpose was to measure any adverse effect (if one exists) of hormone replacement therapy administered to breast cancer survivors. STUDY DESIGN: Forty-one patients from a group of 77 patients who received hormone replacement therapy after therapy for breast cancer were matched with 82 comparison patients not receiving hormone replacement therapy. Both groups were taken from the same population on the basis of cancer registry of the Cancer Surveillance Program of Orange County and were compared with regard to survival results. RESULTS: An analysis of survival time and disease-free time revealed no statistically significant difference between the two groups. CONCLUSIONS: No obvious adverse effect of hormone replacement therapy could be shown in this pilot study. A case is made for a prospective randomized trial. __________________________ ___________________________ Am J Obstet Gynecol. 2002 Aug;187(2):289-94; discussion 294-5. Estrogen replacement therapy in patients with early breast cancer . Natrajan PK, Gambrell RD Jr. Reproductive Endocrinologists, Augusta, GA 30910, USA. OBJECTIVE: Most physicians believe that estrogen replacement therapy is contraindicated once a patient is diagnosed with breast cancer. Recently, several studies have shown that estrogen replacement therapy may be safely used in patients with early breast cancer that has been treated successfully. These women can have severe menopausal symptoms and are at risk for osteoporosis. We reviewed the current status of women in our practice with breast cancer who received estrogen replacement therapy, who did not receive hormone replacement therapy, and who did not receive estrogenic hormone replacement therapy. STUDY DESIGN: The study group consisted of 123 women (mean age, 65.4 +/- 8.85 years) who were diagnosed with breast cancer in our practice, including 69 patients who received estrogen replacement therapy for < or = 32 years after diagnosis. The comparative groups were 22 women who used nonestrogenic hormones for < or = 18 years and 32 women who used no hormones for < or = 12 years. The group who did not receive estrogenic hormone replacement therapy received androgens with or without progestogens (such as megestrol acetate). Of the 63 living hormone users, 56 women are still being treated in our clinic, as are 15 of the 22 subjects who receive nonestrogenic hormone replacement therapy. Follow-up was done through the tumor registry at University Hospital; those patients whose tumor records were not current were contacted by telephone. RESULTS: There were 18 deaths in the 123 patients: 6 patients who received estrogen replacement therapy (8.69%), 2 patients who received nonestrogenic hormone replacement therapy (9.09%), and 10 patients who received no hormone replacement therapy (31.25%). Of the 18 deaths, 9 deaths were from breast cancer (mortality rate, 7.3%); 3 deaths were from lung cancer; 1 death was from endometrial cancer; 1 death was from myocardial infarction; 1 death was from renal failure; and 3 deaths were from cerebrovascular accidents. The 9 deaths from breast cancer included one patient who received nonestrogenic hormone replacement therapy (mortality rate, 4.5%), 6 patients who received no hormone replacement therapy (mortality rate, 11.3%), and 2 patients who received estrogen replacement therapy (mortality rate, 4.28%). The 9 non- breast cancer deaths included 4 patients who received estrogen replacement therapy (endometrial cancer [1 death], lung cancer [1 death], cerebrovascular accident [1 death], and renal failure [1 death]), 1 patient who did not receive estrogenic hormone replacement therapy group (myocardial infarction), and 4 patients who used no hormones (lung cancer, 2 deaths; stroke, 2 deaths). Carcinoma developed in one patient in the estrogen replacement therapy group in the contralateral breast after 4 years of hormone replacement therapy; she is living and well 2.5 years later with no evidence of disease. Metastatic breast cancer developed in one patient after 8 years of hormone replacement therapy; she is living with disease. CONCLUSION: Estrogen replacement therapy apparently does not increase either the risk of recurrence or of death in patients with early breast cancer. These patients may be offered estrogen replacement therapy after a full explanation of the benefits, risks, and controversies. ___________________________ Rev Med Liege. 2003 Feb;58(2):77-82. Hormone replacement therapy after breast cancer. Yes...or no? [Article in French] Foidart JM, Desreux J, Lifrange E, Colin C. Departement de Gynecologie-Obstetrique-Senologie, CHU de Liege. Clinical and experimental studies indicate that combined unique conjugated estrogens and medroxyprogesterone acetate moderately increase the risk of breast cancer in postmenopausal women. Classically, hormone replacement therapy is contra-indicated in women with a past history of breast cancer due to the fear of recurrence. However, these postmenopausal patients complain about hot flushes and adjuvant hormonal therapies (such as aromatase inhibitors, SERMs and Tamoxifen...) aggravate their symptoms. "Observational studies and their meta-analyses do not show a deleterious effect but rather a beneficial impact of hormone replacement therapy among women with a past history of breast cancer." We summarise all these studies and their biological, clinical and epidemiological interpretations. We conclude that short term hormone replacement therapy is safe among those women requesting a replacement therapy after complete information. It is however advisable to conclude definitely only when prospective randomised trials with estradiol or tibolone (a promising alternative) will be available. Such ongoing studies will allow to conclude definitely the possible benefits and risks of hormone replacement therapy among patients with a past history of breast cancer. __________________________ Int J Gynaecol Obstet. 1999 Jan;64(1):59-63. Estrogen replacement therapy in breast cancer survivors. Guidozzi F. Department of Obstetrics and Gynaecology, Johannesburg Hospital, University of the Witwatersrand Medical School, South Africa. OBJECTIVE: To determine whether estrogen replacement therapy (ERT) adversely affected outcome of breast cancer survivors. METHOD: A prospective descriptive study of all breast cancer survivors who requested ERT because of intractable menopausal symptoms. All patients presented voluntarily as gynecological outpatients and were all given oral continuous opposed ERT: 20 premarin and medroxyprogesterone and four tibolone. RESULTS: Twenty-four patients who had previously been treated for breast cancer 8-91 months prior to their initiating ERT have been observed for 24-44 months. There were 15 patients with stage 1, eight with stage 2 and one with stage 4 breast cancer. The mean age of the patients at commencement of ERT was 48 years (range 42-61). Two patients had a biopsy of a suspicious breast nodule: both of which were benign. There have not been any recurrences to date. CONCLUSION: Breast cancer survivors did not have their outcome adversely affected by ERT during an observation period of 24-44 months ------------------------- Gynecol Endocrinol. 2002 Dec;16(6):469-78. Hormone replacement therapy in women with a history of breast cancer. Ylikorkala O, Metsa-Heikkila M. Department of Obstetrics and Gynecology, Helsinki University Central Hospital, Helsinki, Finland. Health care professionals in modern Western societies will meet an increasing number of women surviving breast cancer. How the menopause of these women should be treated is still an open question. Use of hormone replacement therapy (HRT) may, at least in theory, increase the risk for recurrence of cancer, but its categoric refusal is a double-edged sword because it also denies these women all the indisputable health benefits HRT provides. This refusal is not, however, supported by the observational data available so far on this question, because HRT has not increased the risk for breast cancer recurrence. In fact, it is well established that HRT abolishes hot flushes and improves significantly these patients' quality of life. At present, we have no effective nonhormonal alternatives for the control of vasomotor symptoms, and the efficacy of phytoestrogens in the treatment of menopausal symptoms is unproven. Selective estrogen receptor modulators (SERMs) which protect against osteoporosis and perhaps also against breast cancer, and which may have beneficial effects on the cardiovascular system, aggravate hot flushes and are therefore not useful, at least in the first postmenopausal years. In some countries, progestins are often prescribed for the control of such patients' vasomotor symptoms, but their safety has never been assessed in clinical trials, and in theory they can be harmful. Randomized clinical trials (RCT) on the use of HRT in breast cancer survivors are underway, but their completion will take years, and even these may be open to criticism. Tibolone may appear to be an appealing alternative for HRT, but it should also be studied with RCTs in this indication. At present, a patient with a history of breast cancer must be given balanced information as to the possible benefits and risks of HRT, and she herself must make the decision whether or not to start HRT. Int J Fertil Womens Med. 1999 Jun-Aug;44(4):186-92. An experience with estrogen replacement therapy in breast cancer survivors. Brewster WR, DiSaia PJ, Grosen EA, McGonigle KF, Kuykendall JL, Creasman WT. Division of Gynecologic Oncology, University of California Irvine Medical Center, Orange 92868, USA. OBJECTIVE: To evaluate the outcome of breast cancer patients who elected estrogen replacement therapy (ERT). STUDY DESIGN: Breast cancer survivors who elected ERT received the preferred regimen of conjugated estrogen 0.625 mg/day with medroxyprogesterone acetate 2.5 mg/day. RESULTS: 145 patients received ERT for at least 3 months. Thirteen recurrences (9%) were identified; 10 are alive with disease, 3 are dead of disease. The median interval between diagnosis and commencement of ERT was 41 months. Forty-one percent of the study group initiated ERT within 3 years of their breast cancer diagnosis. The median duration of follow-up on ERT was 30 months. CONCLUSION: The concern that ERT might activate growth in occult metastatic sites and promote a rash of recurrences was not confirmed. It is unreasonable to categorically deny all breast cancer survivors ERT. J Reprod Med. 2004 Jul;49(7):510-26. Hormone therapy for women after breast cancer: a review Levgur M. Department of Obstetrics and Gynecology, Maimonides Medical Center, Brooklyn, NY 11219, USA Even though it is accepted that women with breast cancer should not receive estrogen therapy, doubts have been expressed as to the validity of this policy. In recent years opposition to this practice has been voiced more adamantly. The results of the Women's Health Initiative (WHI) study, published in July 2002,question the safety margin of estrogen therapy (ET) or hormone therapy (HT) in menopause. Whether this concern is applicable to breast cancer survivors is unclear as these women were not addressed bythe study. In light of the uncertainties raised by the study and particularly the ongoing controversy about breast cancer patients, a review of the literature published prior to March 2003 was undertaken. The information gathered on the topic comes from 10 uncontrolled studies and 11 case-controlled studies, 8retrospective and 3 prospective, carried out over the past decade. The experience encompasses 1,558 breast cancer survivors treated with ET or HT. Overall, the recurrence rate accrued from the uncontrolled studies is 7.3% (53 of 728). The average rate culminating from 11 case-controlled studies is 10.7% (99 of 830) (2.6-15.4%) in treated patients vs. 20.3% (739 of 3,640) (2.3-29.5%) in their untreated counterparts. This review revealed no increase in recurrent disease among treated patients but is not conclusive as some studies that have been flawed by biases and confounders. The fact that only 2 studies were case controlled and prospective as well as randomized, and considering concerns raised by the WHI study, it seems that many more such trials will be necessary before this controversial issue will be settled ---------------------------------------------------- Ann Surg Oncol. 2001 Dec;8(10):828-32. Estrogen replacement therapy after breast cancer: a 12-year follow-up. Peters GN, Fodera T, Sabol J, Jones S, Euhus D. The Center for Breast Care, The University of Texas Southwestern Medical Center at Dallas, 75390-9161, USA. BACKGROUND: In the United States, estrogen replacement therapy (ERT) is discouraged in breast cancer survivors because of concerns that hormones may reactivate the disease. Because ERT can improve quality of life and decrease morbidity from osteoporosis and cardiovascular disease, however, this policy is increasingly being challenged. METHODS: From February to August 1995, 607 breast cancer survivors were interviewed concerning ERT usage. Sixty-four patients indicated they received some form of ERT after their breast cancer diagnosis. Medical records for these patients were analyzed for disease stage, surgical treatment, adjuvant treatment, estrogen and progesterone receptor status, date of initiation of ERT, type of ERT, recurrence, and final outcome. Patients receiving ERT were followed prospectively. RESULTS: Eight patients were excluded because they had used only vaginal cream ERT. The remaining 56 received ERT as conjugated estrogens, an estradiol patch, estropipate, or birth control pills. The median follow-up from diagnosis was 12.8 years (range, 4.7-38.9 years). The median time on ERT since diagnosis was 6.4 years (range, 1.0-20.9 years); 38% of the patients initiated ERT within 2 years of diagnosis. Estrogen receptors were positive in 28 (74%) of the 38 cases with available information. Pathological disease stage at time of diagnosis and treatment was 0 in 15 cases (27%), I in 27 (48%), and II in 14 (25%). Twenty-six patients (47%) received adjuvant chemotherapy or hormonal therapy. One local recurrence and one contralateral breast cancer occurred during the follow-up period (13.5 and 9.6 years, respectively), with no regional or distant recurrences, for a 15-year actuarial disease-free survival rate of 92.5%. There were no breast cancer deaths. CONCLUSIONS: Use of ERT in a cohort of breast cancer survivors with tumors of generally good prognosis was not associated with increased breast cancer events compared with non-ERT users, even over a long follow-up period. Anticancer Res. 1998 May-Jun;18(3C):2253-5. Hormone replacement therapy in women with breast cancer. Braendle W. Division of Gynecological Endocrinology and Reproductive Medicine, University Hospital, Hamburg-Eppendorf, Germany. The influence of estrogens on the growth of mammary carcinoma cell lines has been confirmed by many studies. Therefore, past or recent history of breast cancer is principally seen as a contraindication for estrogen or estrogen/progestin replacement therapy. The recently made possible early diagnosis of mammary carcinomas in many cases has resulted in a better prognosis, and means that following treatment women are living for a long time postmenopausally. Therefore, hormone replacement therapy is demanded by many patients. Recent studies with a limited number of patients, however, have shown no adverse effects of an estrogen or an estrogen-progestin replacement therapy after treatment of a mammary carcinoma. In some studies even a positive effect has been found in recurrence free survival. However, a final decision upon estrogen or estrogen/progestin replacement therapy in postmenopausal women with a history of breast cancer, cannot be made until the results of prospective clinical trials are finalized. ------------------------------------------------------- Menopause. 2003 Jul-Aug;10(4):277-85. Estrogen replacement therapy in breast cancer survivors: a matched- controlled series. Decker DA, Pettinga JE, VanderVelde N, Huang RR, Kestin L, Burdakin JH. Department of Medicine, William Beaumont Hospital, Royal Oak-Troy, MI 48073, USA OBJECTIVE: We prospectively administered estrogen replacement therapy (ERT) to control estrogen deficiency symptoms in breast cancer survivors as part of our clinical practice. We report the consequences of ERT compared with a historical matched-control group. DESIGN: Two hundred seventy-seven disease-free survivors received ERT. Controls were matched for exact stage, a recurrence-free period similar to the period to ERT initiation in the ERT group, approximate age, and duration of follow-up. The mean time from breast cancer diagnosis to initiation of ERT was 3.61 (+/- 0.25) years, with a median of 1.88 years. The mean duration of ERT was 3.7 (+/- 3.01) years, with a median of 3.05 years. RESULTS: Hot flashes were relieved in 206 of 223 women (92%), dyspareunia/vaginal dryness in 149 of 167 women (89%), and reactive depression/anxiety/mood change in 111 of 126 women (88%). Univariate analysis demonstrated no statistical differences between the groups for age, stage, pathology at diagnosis, progesterone receptor status, local therapy, breast at risk, prior chemotherapy, and duration of follow-up. The ERT group was more likely to be estrogen receptor negative (P = 0.01), to have received prior ERT (P < 0.001), and to have received no adjuvant tamoxifen (P < 0.001). There was no significant difference between the ERT and control groups in ipsilateral primary/recurrence (5/155 v 5/143; P = 0.85), contralateral breast cancers (10/258 v 9/260; P = 0.99), or systemic metastasis (8/277 v 15/277; P = 0.13). Noncause-specific deaths in the control group numbered 15 (of 277), and in the ERT group, 7 (of 277) (P = 0.03). Overall survival favored the ERT group (P = 0.02). CONCLUSIONS: In these selected patients, ERT relieved estrogen deficiency symptoms and did not increase the rate or time to an ipsilateral recurrence/new primary, contralateral new primary, local-regional recurrence, or systemic metastases. - Jeffrey Dach MD 7450 Griffin Road, Suite 190 Davie, Fl 33314 954-792-4663 www.jeffreydach.com www.drdach.com www.naturalmedicine101.com www.bioidenticalhormones101.com www.truemedmd.com Click Here for: Dr Dach's Online Store for Pure Encapsulations Supplements Click Here for: Dr Dach's Online Store for Nature's Sunshine Supplements Web Site and Discussion Board Links: jdach1.typepad.com/blog/ disc.yourwebapps.com/Indices/244124.html disc.yourwebapps.com/Indices/244066.html disc.yourwebapps.com/Indices/244067.html disc.yourwebapps.com/Indices/244161.html disc.yourwebapps.com/Indices/244163.html additional links: http://www.health-forums.com/alt-support-cancer-breast/bone-scan-v-pet-scan-18715.html#post150479 Re: bone scan v. PET scanhttp://www.health-forums.com/alt-support-cancer-breast/bone-scan-v-pet-scan-18715.html#post151685 http://www.health-forums.com/misc-fitness-weights/jarvik-heart-lipitor-jeffrey-dach-6671.html Jarvik Heart and Lipitor by jeffrey dachLipitor Ad Campaign with Jarvik Heart by jeffrey dach http://www.health-forums.com/alt-support-anxiety-panic/depression-anxiety-panic-attacks-6317.html Depression, Anxiety and Panic AttacksNatural Medicine 101 the book by jeffrey dach md Natural Medicine 101 the book by jeffrey dach md A new book Natural Medicine 101 http://www.health-forums.com/alt-support-cancer-breast/bone-scan-v-pet-scan-18715.html#post150479 Re: bone scan v. PET scanhttp://www.health-forums.com/alt-support-cancer-breast/bone-scan-v-pet-scan-18715.html#post151685 http://www.health-forums.com/misc-fitness-weights/jarvik-heart-lipitor-jeffrey-dach-6671.html Jarvik Heart and Lipitor by jeffrey dachLipitor Ad Campaign with Jarvik Heart by jeffrey dach http://www.health-forums.com/alt-support-anxiety-panic/depression-anxiety-panic-attacks-6317.html Depression, Anxiety and Panic AttacksNatural Medicine 101 the book by jeffrey dach md Natural Medicine 101 the book by jeffrey dach md Disclaimer click here: www.drdach.com/wst_page20.html The reader is advised to discuss the comments on these pages with his/her personal physicians and to only act upon the advice of his/her personal physician. Also note that concerning an answer which appears as an electronically posted question, I am NOT creating a physician -- patient relationship. Although identities will remain confidential as much as possible, as I can not control the media, I can not take responsibility for any breaches of confidentiality that may occur. Link to this article Copyright (c) 2012-2014 Jeffrey Dach MD All Rights Reserved. This article may be reproduced on the internet without permission, provided there is a link to this page and proper credit is given. FAIR USE NOTICE: This site contains copyrighted material the use of which has not always been specifically authorized by the copyright owner. We are making such material available in our efforts to advance understanding of issues of significance. We believe this constitutes a 'fair use' of any such copyrighted material as provided for in section 107 of the US Copyright Law. In accordance with Title 17 U.S.C. Section 107, the material on this site is distributed without profit to those who have expressed a prior interest in receiving the included information for research and educational purposes. |
