Tamoxifen and Risk of Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers

被引:141
作者
Phillips, Kelly-Anne [1 ,2 ]
Milne, Roger L. [2 ,4 ]
Rookus, Matti A. [6 ]
Daly, Mary B. [9 ]
Antoniou, Antonis C. [10 ]
Peock, Susan [10 ]
Frost, Debra [10 ]
Easton, Douglas F. [10 ]
Ellis, Steve [10 ]
Friedlander, Michael L. [3 ]
Buys, Saundra S. [11 ]
Andrieu, Nadine [12 ,13 ,16 ]
Nogues, Catherine [17 ]
Stoppa-Lyonnet, Dominique [12 ,14 ,15 ]
Bonadona, Valerie [18 ,19 ,20 ]
Pujol, Pascal [21 ,22 ]
McLachlan, Sue Anne [1 ,2 ]
John, Esther M. [23 ,24 ]
Hooning, Maartje J. [7 ]
Seynaeve, Caroline [7 ]
Tollenaar, Rob A. E. M. [8 ]
Goldgar, David E. [11 ]
Terry, Mary Beth [25 ]
Caldes, Trinidad [5 ]
Weideman, Prue C. [1 ]
Andrulis, Irene L. [26 ]
Singer, Christian F. [29 ]
Birch, Kate [1 ]
Simard, Jacques [27 ,28 ]
Southey, Melissa C. [2 ]
Olsson, Hakan L. [30 ]
Jakubowska, Anna [31 ]
Olah, Edith [32 ]
Gerdes, Anne-Marie [33 ,34 ]
Foretova, Lenka [35 ]
Hopper, John L. [2 ]
机构
[1] Peter MacCallum Canc Ctr, Melbourne, Vic 8006, Australia
[2] Univ Melbourne, Melbourne, Vic, Australia
[3] Prince Wales Hosp, Randwick, NSW 2031, Australia
[4] Spanish Natl Canc Res Ctr, Madrid, Spain
[5] Hosp Clin San Carlos, Inst Invest Sanitaria San Carlos, Madrid, Spain
[6] Netherlands Canc Inst, Amsterdam, Netherlands
[7] Erasmus Univ, Med Ctr, Daniel den Hoed Canc Ctr, Rotterdam, Netherlands
[8] Leiden Univ, Med Ctr, Leiden, Netherlands
[9] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[10] Univ Cambridge, Cambridge, England
[11] Univ Utah, Huntsman Canc Inst, Salt Lake City, UT 84112 USA
[12] Inst Curie, Paris, France
[13] INSERM, U900, Paris, France
[14] INSERM, U830, Paris, France
[15] Univ Paris 05, Paris, France
[16] Mines ParisTech, Fontainebleau, France
[17] Hop Rene Huguenin, Inst Curie, St Cloud, France
[18] Univ Lyon 1, F-69365 Lyon, France
[19] CNRS, Unite Mixte Rech 5558, Lyon, France
[20] Ctr Leon Berard, Lyon, France
[21] Ctr Hosp Univ Arnaud de Villeneuve, Montpellier, France
[22] Inst Natl Sante & Rech Med 896, Ctr Rech Cancerol Marseille Val dAurelle, Montpellier, France
[23] Canc Prevent Inst Calif, Fremont, CA USA
[24] Stanford Univ, Sch Med, Stanford, CA 94305 USA
[25] Columbia Univ, New York, NY USA
[26] Univ Toronto, Toronto, ON, Canada
[27] Ctr Hosp Univ Quebec, Quebec City, PQ, Canada
[28] Univ Laval, Quebec City, PQ, Canada
[29] Med Univ Vienna, Vienna, Austria
[30] Lund Univ, Lund, Sweden
[31] Pomeranian Med Univ, Szczecin, Poland
[32] Natl Inst Oncol, Budapest, Hungary
[33] Rigshosp, DK-2100 Copenhagen, Denmark
[34] Univ Copenhagen, Copenhagen, Denmark
[35] Masaryk Mem Canc Inst, Brno, Czech Republic
基金
加拿大健康研究院; 美国国家卫生研究院; 英国医学研究理事会;
关键词
ESTROGEN-RECEPTOR-BETA; SURGICAL ADJUVANT BREAST; OVARIAN-CANCER; PREVENTION TRIAL; SALPINGO-OOPHORECTOMY; ENDOMETRIAL CANCER; REDUCING SURGERY; FOLLOW-UP; WOMEN; SURVEILLANCE;
D O I
10.1200/JCO.2012.47.8313
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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.
引用
收藏
页码:3091 / 3099
页数:9
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