Tamoxifen and Risk of Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
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Published:2013-09-01
Issue:25
Volume:31
Page:3091-3099
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ISSN:0732-183X
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Container-title:Journal of Clinical Oncology
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language:en
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Short-container-title:JCO
Author:
Phillips Kelly-Anne1, Milne Roger L.1, Rookus Matti A.1, Daly Mary B.1, Antoniou Antonis C.1, Peock Susan1, Frost Debra1, Easton Douglas F.1, Ellis Steve1, Friedlander Michael L.1, Buys Saundra S.1, Andrieu Nadine1, Noguès Catherine1, Stoppa-Lyonnet Dominique1, Bonadona Valérie1, Pujol Pascal1, McLachlan Sue Anne1, John Esther M.1, Hooning Maartje J.1, Seynaeve Caroline1, Tollenaar Rob A.E.M.1, Goldgar David E.1, Terry Mary Beth1, Caldes Trinidad1, Weideman Prue C.1, Andrulis Irene L.1, Singer Christian F.1, Birch Kate1, Simard Jacques1, Southey Melissa C.1, Olsson Håkan L.1, Jakubowska Anna1, Olah Edith1, Gerdes Anne-Marie1, Foretova Lenka1, Hopper John L.1
Affiliation:
1. Kelly-Anne Phillips, Sue Anne McLachlan, Prue C. Weideman, and Kate Birch, Peter MacCallum Cancer Centre; Kelly-Anne Phillips, Roger L. Milne, Sue Anne McLachlan, Melissa C. Southey, and John L. Hopper, University of Melbourne; Sue Anne McLachlan, St Vincent's Hospital, Melbourne, Victoria; Michael L. Friedlander, Prince of Wales Hospital, Randwick, New South Wales, Australia; Roger L. Milne, Spanish National Cancer Research Centre; Trinidad Caldes, Hospital Clinico San Carlos, Instituto de Investigación...
Abstract
Purpose To determine whether adjuvant tamoxifen treatment for breast cancer (BC) is associated with reduced contralateral breast cancer (CBC) risk for BRCA1 and/or BRCA2 mutation carriers. Methods Analysis of pooled observational cohort data, self-reported at enrollment and at follow-up from the International BRCA1, and BRCA2 Carrier Cohort Study, Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer, and Breast Cancer Family Registry. Eligible women were BRCA1 and BRCA2 mutation carriers diagnosed with unilateral BC since 1970 and no other invasive cancer or tamoxifen use before first BC. Hazard ratios (HRs) for CBC associated with tamoxifen use were estimated using Cox regression, adjusting for year and age of diagnosis, country, and bilateral oophorectomy and censoring at contralateral mastectomy, death, or loss to follow-up. Results Of 1,583 BRCA1 and 881 BRCA2 mutation carriers, 383 (24%) and 454 (52%), respectively, took tamoxifen after first BC diagnosis. There were 520 CBCs over 20,104 person-years of observation. The adjusted HR estimates were 0.38 (95% CI, 0.27 to 0.55) and 0.33 (95% CI, 0.22 to 0.50) for BRCA1 and BRCA2 mutation carriers, respectively. After left truncating at recruitment to the cohort, adjusted HR estimates were 0.58 (95% CI, 0.29 to 1.13) and 0.48 (95% CI, 0.22 to 1.05) based on 657 BRCA1 and 426 BRCA2 mutation carriers with 100 CBCs over 4,392 person-years of prospective follow-up. HRs did not differ by estrogen receptor status of the first BC (missing for 56% of cases). Conclusion This study provides evidence that tamoxifen use is associated with a reduction in CBC risk for BRCA1 and BRCA2 mutation carriers. Further follow-up of these cohorts will provide increased statistical power for future prospective analyses.
Publisher
American Society of Clinical Oncology (ASCO)
Subject
Cancer Research,Oncology
Cited by
147 articles.
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