Tamoxifen and contralateral breast cancer in BRCA1 and BRCA2 carriers:: an update

被引:182
作者
Gronwald, J
Tung, N
Foulkes, WD
Offit, K
Gershoni, R
Daly, M
Kim-Sing, C
Olsson, H
Ainsworth, P
Eisen, A
Saal, H
Friedman, E
Olopade, O
Osborne, M
Weitzel, J
Lynch, H
Ghadirian, P
Lubinski, J
Sun, P
Narod, SA
机构
[1] Univ Toronto, Ctr Res Womens Hlth, Toronto, ON M5G 1N8, Canada
[2] Pomeranian Med acad, Hereditary Canc Ctr, Dept Genet & Pathol, Szczecin, Poland
[3] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[4] Montreal Gen Hosp, Div Med Genet, Montreal, PQ H3G 1A4, Canada
[5] Mem Sloan Kettering Canc Ctr, Dept Human Genet & Med, New York, NY 10021 USA
[6] Rambam Med Ctr, Haifa, Israel
[7] Fox Chase Canc Ctr, Cheltenham, PA USA
[8] Vancouver Ctr BC Canc Agcy, Vancouver, BC, Canada
[9] Univ Lund Hosp, Dept Oncol, Jubileum Inst, S-22185 Lund, Sweden
[10] London Hlth Sci Ctr, London, ON, Canada
[11] Sunnybrook & Womens Coll, Hlth Sci Ctr, Dept Med Oncol, Toronto, ON, Canada
[12] Childrens Hosp, Med Ctr, Cincinnati, OH 45229 USA
[13] Chaim Sheba Med Ctr, Oncogenet Unit, IL-52621 Tel Hashomer, Israel
[14] Univ Chicago, Ctr Clin Canc Genet, Chicago, IL 60637 USA
[15] Strang Canc Prevent Ctr, New York, NY USA
[16] City Hope Natl Med Ctr, Duarte, CA 91010 USA
[17] Creighton Univ, Sch Med, Dept Prevent Med & Publ Hlth, Omaha, NE 68178 USA
[18] Univ Montreal, Epidemiol Res Unit, CHUM, Montreal, PQ, Canada
关键词
breast cancer; tamoxifen; oophorectomy; BRCA1; BRCA2;
D O I
10.1002/ijc.21536
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Women with a mutation in BRCA1 or BRCA2 face a lifetime risk of breast cancer of similar to 80%, and following the first diagnosis the 10-year risk of contralateral breast cancer is similar to 30%. It has been shown that both tamoxifen and oophorectomy prevent contralateral breast cancer, but it is not clear whether there is a benefit in giving tamoxifen to women who have previously undergone an oophorectomy. Furthermore, the relative degree of protection in BRCA1 and BRCA2 carriers has not been well evaluated. We studied 285 women with bilateral breast cancer and a BRCA1 or BRCA2 mutation, and 751 control women with unilateral breast cancer and a BRCA1 or BRCA2 mutation in a matched case-control study. Control women were of similar age and had a similar age of diagnosis of breast cancer and had been followed for as long as the case for a second primary breast cancer. The history of tamoxifen use for treating the first breast cancer was compared between bilateral and unilateral cases. The multivariate odds ratio for contralateral breast cancer associated with tamoxifen use was 0.50 for carriers of BRCA1 mutations (95% CI, 0.304.85) and was 0.42 for carriers of BRCA2 mutations (95% CI, 0.17-1.02). The protective effect of tamoxifen was not seen among women who had undergone an oophorectomy (OR = 0.83; 95% CI, 0.242.89) but this subgroup was small. In contrast, a strong protective effect of tamoxifen was apparent among women who were premenopausal or who had undergone natural menopause (OR = 0.44; 95% CI, 0.27-0.65). (c) 2005 Wiley-Liss, Inc.
引用
收藏
页码:2281 / 2284
页数:4
相关论文
共 20 条
[1]  
EISEN A, IN PRESS J CLIN ONCO
[2]  
Eisinger F, 1999, CANCER-AM CANCER SOC, V85, P2291, DOI 10.1002/(SICI)1097-0142(19990515)85:10<2291::AID-CNCR26>3.0.CO
[3]  
2-9
[4]   A RANDOMIZED CLINICAL-TRIAL EVALUATING TAMOXIFEN IN THE TREATMENT OF PATIENTS WITH NODE-NEGATIVE BREAST-CANCER WHO HAVE ESTROGEN-RECEPTOR POSITIVE TUMORS [J].
FISHER, B ;
COSTANTINO, J ;
REDMOND, C ;
POISSON, R ;
BOWMAN, D ;
COUTURE, J ;
DIMITROV, NV ;
WOLMARK, N ;
WICKERHAM, DL ;
FISHER, ER ;
MARGOLESE, R ;
ROBIDOUX, A ;
SHIBATA, H ;
TERZ, J ;
PATERSON, AHG ;
FELDMAN, MI ;
FARRAR, W ;
EVANS, J ;
LICKLEY, HL ;
KETNER, M .
NEW ENGLAND JOURNAL OF MEDICINE, 1989, 320 (08) :479-484
[5]   Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families [J].
Ford, D ;
Easton, DF ;
Stratton, M ;
Narod, S ;
Goldgar, D ;
Devilee, P ;
Bishop, DT ;
Weber, B ;
Lenoir, G ;
Chang-Claude, J ;
Sobol, H ;
Teare, MD ;
Struewing, J ;
Arason, A ;
Scherneck, S ;
Peto, J ;
Rebbeck, TR ;
Tonin, P ;
Neuhausen, S ;
Barkardottir, R ;
Eyfjord, J ;
Lynch, H ;
Ponder, BAJ ;
Gayther, SA ;
Birch, JM ;
Lindblom, A ;
Stoppa-Lyonnet, D ;
Bignon, Y ;
Borg, A ;
Hamann, U ;
Haites, N ;
Scott, RJ ;
Maugard, CM ;
Vasen, H .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (03) :676-689
[6]   Tumour biological features of BRCA1-induced breast and ovarian cancer [J].
Johannsson, OT ;
Idvall, I ;
Anderson, C ;
Borg, A ;
Barkardottir, RB ;
Egilsson, V ;
Olsson, H .
EUROPEAN JOURNAL OF CANCER, 1997, 33 (03) :362-371
[7]  
Karp SE, 1997, CANCER-AM CANCER SOC, V80, P435, DOI 10.1002/(SICI)1097-0142(19970801)80:3<435::AID-CNCR11>3.0.CO
[8]  
2-Y
[9]   Tamoxifen and breast cancer incidence among women with inherited mutations in BRCA1 and BRCA2 -: National Surgical Adjuvant Breast and Bowel Project (NSABP-P1) Breast Cancer Prevention Trial [J].
King, MC ;
Wieand, S ;
Hale, K ;
Lee, M ;
Walsh, T ;
Owens, K ;
Tait, J ;
Ford, L ;
Dunn, BK ;
Costantino, J ;
Wickerham, L ;
Wolmark, N ;
Fisher, B .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (18) :2251-2256
[10]  
Lakhani SR, 1997, LANCET, V349, P1505