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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

  • Timothy R. Rebbeck
  • , Tara Friebel
  • , Theresa Wagner
  • , Henry T. Lynch
  • , Judy E. Garber
  • , Mary B. Daly
  • , Claudine Isaacs
  • , Olufunmilayo I. Olopade
  • , Susan L. Neuhausen
  • , Laura Van't Veer
  • , Rosalind Eeles
  • , D. Gareth Evans
  • , Gail Tomlinson
  • , Ellen Matloff
  • , Steven A. Narod
  • , Andrea Eisen
  • , Susan Domchek
  • , Katrina Armstrong
  • , Barbara L. Weber
  • University of Pennsylvania

Research output: Contribution to journalArticlepeer-review

407 Scopus citations

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 BRCA 1/2 mutation carriers.

Original languageEnglish
Pages (from-to)7804-7810
Number of pages7
JournalJournal of Clinical Oncology
Volume23
Issue number31
DOIs
StatePublished - Nov 1 2005

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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