Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2006-2-27
pubmed:abstractText
Women with a mutation in BRCA1 or BRCA2 face a lifetime risk of breast cancer of approximately 80%, and following the first diagnosis the 10-year risk of contralateral breast cancer is approximately 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).
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
May
pubmed:issn
0020-7136
pubmed:author
pubmed:copyrightInfo
2005 Wiley-Liss, Inc.
pubmed:issnType
Print
pubmed:day
1
pubmed:volume
118
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2281-4
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed-meshheading:16331614-Adult, pubmed-meshheading:16331614-Antineoplastic Agents, Hormonal, pubmed-meshheading:16331614-Breast Neoplasms, pubmed-meshheading:16331614-Case-Control Studies, pubmed-meshheading:16331614-DNA Mutational Analysis, pubmed-meshheading:16331614-Female, pubmed-meshheading:16331614-Functional Laterality, pubmed-meshheading:16331614-Genes, BRCA1, pubmed-meshheading:16331614-Genes, BRCA2, pubmed-meshheading:16331614-Genetic Predisposition to Disease, pubmed-meshheading:16331614-Humans, pubmed-meshheading:16331614-Middle Aged, pubmed-meshheading:16331614-Neoplasms, Second Primary, pubmed-meshheading:16331614-Odds Ratio, pubmed-meshheading:16331614-Pedigree, pubmed-meshheading:16331614-Premenopause, pubmed-meshheading:16331614-Retrospective Studies, pubmed-meshheading:16331614-Risk Assessment, pubmed-meshheading:16331614-Tamoxifen
pubmed:year
2006
pubmed:articleTitle
Tamoxifen and contralateral breast cancer in BRCA1 and BRCA2 carriers: an update.
pubmed:affiliation
Hereditary Cancer Center, Department of Genetics and Pathology, Pomeranian Medical Academy, Szczecin, Poland.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, Non-P.H.S., Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural