TY - JOUR
T1 - Tamoxifen and risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers
T2 - A case-control study
AU - Narod, Steven A.
AU - Brunet, Jean Sébastien
AU - Ghadirian, Parviz
AU - Robson, Mark
AU - Heimdal, Ketil
AU - Neuhausen, Susan L.
AU - Stoppa-Lyonnet, Dominique
AU - Lerman, Caryn
AU - Pasini, Barbara
AU - De Los Rios, Patricia
AU - Weber, Barbara
AU - Lynch, Henry
N1 - Funding Information:
This study was supported by the US National Institutes of Health grants 1R01 CA63682, CA63678, CA57601, CA61231, and CA74415, the National Cancer Institute of Canada Breast Cancer Initiative, the Department of the Army grants DAMD17-94-J-4299, DAMD 17-94-J-4260, and DAMD 17-97-J 4340, the Canadian Genetics Diseases Network, the Canadian Breast Cancer Foundation (Ontario Chapter), the Fonds de La Recherche en Sante du Quebec, the Ontario Cancer Genetics Network, the Women's Cancer Program of the Dana Farber Cancer Institute, the Norwegian Cancer Society, the Italian Association and Foundation for Cancer Research (Special Project: Hereditary Tumours), the Society of Memorial Sloan-Kettering Cancer Center, the Utah Cancer Registry, and the Utah Department of Health. MR is the recipient of an American Cancer Society Physicians Training Award PRTA-38.
PY - 2000/12/2
Y1 - 2000/12/2
N2 - Background: Women with a mutation in BRCA1 or BRCA2 have a high risk of developing breast cancer and of contralateral cancer after the initial diagnosis of breast cancer. Tamoxifen protects against contralateral breast cancer in the general population, but whether it protects against contralateral breast cancer in BRCA1 or BRCA2 mutation carriers is not known. Methods: We compared 209 women with bilateral breast cancer and BRCA1 or BRCA2 mutation (bilateral-disease cases), with 384 women with unilateral disease and BRCA1 or BRCA2 mutation (controls) in a matched case-control study. Age and age at diagnosis of breast cancer (range 24-74 years) were much the same in bilateral-disease cases and controls, and both groups had been followed up for the same time for a second primary breast cancer. History of tamoxifen use for first breast cancer was obtained by interview, or by self-administered questionnaire. Findings: The multivariate odds ratio for contralateral breast cancer associated with tamoxifen use was 0-50 (95% Cl 0.28-0.89). Tamoxifen protected against contralateral breast cancer for carriers of BRCA1 mutations (odds ratio 0.38, 95% Cl 0-19-0-74) and for those with BRCA2 mutations (0.63, 0-20-1-50). In women who used tamoxifen for 2-4 years, the risk of contralateral breast cancer was reduced by 75%. A reduction in risk of contralateral cancer was also seen with oophorectomy (0.42, 0-22-0.83) and with chemotherapy (0 40, 0-26-0.60). Interpretation: Tamoxifen use reduces the risk of contralateral breast cancer in women with pathogenic mutations in the BRCA1 or BRCA2 gene. The protective effect of tamoxifen seems independent of that of oophorectomy.
AB - Background: Women with a mutation in BRCA1 or BRCA2 have a high risk of developing breast cancer and of contralateral cancer after the initial diagnosis of breast cancer. Tamoxifen protects against contralateral breast cancer in the general population, but whether it protects against contralateral breast cancer in BRCA1 or BRCA2 mutation carriers is not known. Methods: We compared 209 women with bilateral breast cancer and BRCA1 or BRCA2 mutation (bilateral-disease cases), with 384 women with unilateral disease and BRCA1 or BRCA2 mutation (controls) in a matched case-control study. Age and age at diagnosis of breast cancer (range 24-74 years) were much the same in bilateral-disease cases and controls, and both groups had been followed up for the same time for a second primary breast cancer. History of tamoxifen use for first breast cancer was obtained by interview, or by self-administered questionnaire. Findings: The multivariate odds ratio for contralateral breast cancer associated with tamoxifen use was 0-50 (95% Cl 0.28-0.89). Tamoxifen protected against contralateral breast cancer for carriers of BRCA1 mutations (odds ratio 0.38, 95% Cl 0-19-0-74) and for those with BRCA2 mutations (0.63, 0-20-1-50). In women who used tamoxifen for 2-4 years, the risk of contralateral breast cancer was reduced by 75%. A reduction in risk of contralateral cancer was also seen with oophorectomy (0.42, 0-22-0.83) and with chemotherapy (0 40, 0-26-0.60). Interpretation: Tamoxifen use reduces the risk of contralateral breast cancer in women with pathogenic mutations in the BRCA1 or BRCA2 gene. The protective effect of tamoxifen seems independent of that of oophorectomy.
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U2 - 10.1016/S0140-6736(00)03258-X
DO - 10.1016/S0140-6736(00)03258-X
M3 - Article
C2 - 11130383
AN - SCOPUS:0034597916
SN - 0140-6736
VL - 356
SP - 1876
EP - 1881
JO - The Lancet
JF - The Lancet
IS - 9245
ER -