4.2 Article

Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations

期刊

FAMILIAL CANCER
卷 11, 期 2, 页码 235-242

出版社

SPRINGER
DOI: 10.1007/s10689-011-9506-2

关键词

BRCA1; BRCA2; Pancreatic cancer; Prostate cancer; Oesophageal cancer; Uveal melanoma

资金

  1. Genesis Breast Cancer Prevention Appeal
  2. NIHR Manchester Biomedical Research Centre
  3. National Institute for Health Research [DHCS/06/06/013] Funding Source: researchfish
  4. National Institutes of Health Research (NIHR) [DHCS/06/06/013] Funding Source: National Institutes of Health Research (NIHR)

向作者/读者索取更多资源

The risks of cancers other than breast and ovarian amongst BRCA1 and BRCA2 mutation carriers are based on relatively few family based studies with the risk of specific cancers tested in population based samples of cancers from founder populations. We assessed risks of other cancers in 268 BRCA1 families and 222 BRCA2 families using a person years at risk analysis from 1975 to 2005. Cancer confirmations were overall higher than in previous family based studies at 64%. There was no overall increase in risk for BRCA1 carriers although oesophagus had a significant increased RR of 2.9 (95% CI 1.1-6.0) and stomach at 2.4 (95% CI 1.2-4.3), these were based mainly on unconfirmed cases. For BRCA2 increased risks for cancers of the pancreas (RR 4.1, 95% CI 1.9-7.8) and prostate (RR 6.3, 95% CI 4.3-9.0) and uveal melanoma (RR 99.4, 95% CI 11.1-359.8) were confirmed. Possible new associations with oesophagus (RR 4.1, 95% CI 1.9-7.8) and stomach (RR 2.7, 95% CI 1.3-4.8) were detected but these findings should be treated with caution due to lower confirmation rates. In contrast to previous research a higher risk of prostate cancer was found in males with mutations in the BRCA2 OCCR region. The present study strengthens the known links between BRCA2 and pancreatic and prostate cancer, but throws further doubt onto any association with BRCA1. New associations with upper gastro-intestinal malignancy need to be treated with caution and confirmed by large prospective studies.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.2
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据