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

Author:

Rebbeck Timothy R.1,Friebel Tara1,Wagner Theresa1,Lynch Henry T.1,Garber Judy E.1,Daly Mary B.1,Isaacs Claudine1,Olopade Olufunmilayo I.1,Neuhausen Susan L.1,van ′t Veer Laura1,Eeles Rosalind1,Evans D. Gareth1,Tomlinson Gail1,Matloff Ellen1,Narod Steven A.1,Eisen Andrea1,Domchek Susan1,Armstrong Katrina1,Weber Barbara L.1

Affiliation:

1. From the Center for Clinical Epidemiology and Biostatistics, Abramson Cancer Center, and Abramson Family Research Institute, The University of Pennsylvania School of Medicine, Philadelphia, PA; Women's College Hospital, Sunnybrook Regional Cancer Centre, Toronto, ON; Medical University of Vienna, Austria; Creighton University, Omaha, NE; Dana-Farber Cancer Institute, Boston, MA; Fox Chase Cancer Center, Philadelphia, PA; Lombardi Cancer Center, Georgetown University, Washington, DC; University of Chicago...

Abstract

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.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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