Tamoxifen and contralateral breast cancer in BRCA1 and BRCA2 carriers: An update Journal Article


Authors: Gronwald, J.; Tung, N.; Foulkes, W. D.; 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, S. A.; Hereditary Breast Cancer Clinical Study Group
Article Title: Tamoxifen and contralateral breast cancer in BRCA1 and BRCA2 carriers: An update
Abstract: Women with a mutation in BRCA1 or BRCA2 face a lifetime risk of breast cancer of ∼80%, and following the first diagnosis the 10-year risk of contralateral breast cancer is ∼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, 0.30-0.85) 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, 0.24-2.89) 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). © 2005 Wiley-Liss, Inc.
Keywords: adult; controlled study; treatment outcome; middle aged; retrospective studies; gene mutation; major clinical study; case-control studies; review; cancer risk; cancer patient; genetic predisposition to disease; cancer prevention; breast cancer; ovariectomy; odds ratio; breast neoplasms; brca1 protein; brca2 protein; heterozygote; risk assessment; pedigree; oncogene; genes, brca1; genes, brca2; tamoxifen; neoplasms, second primary; dna mutational analysis; antineoplastic agents, hormonal; second cancer; premenopause; functional laterality; menopause; brca1; brca2; oral contraceptive agent; drug use; oophorectomy; brca2 gene
Journal Title: International Journal of Cancer
Volume: 118
Issue: 9
ISSN: 0020-7136
Publisher: John Wiley & Sons  
Date Published: 2006-05-01
Start Page: 2281
End Page: 2284
Language: English
DOI: 10.1002/ijc.21536
PUBMED: 16331614
PROVIDER: scopus
DOI/URL:
Notes: - "Export Date: 4 June 2012" - "Source: Scopus"
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  1. Kenneth Offit
    790 Offit