BRCA1 and BRCA2 mutations and the risk for colorectal cancer

结直肠癌 医学 乳腺癌 肿瘤科 癌症 内科学 卵巢癌 突变 结肠镜检查 人口 大肠腺瘤性息肉病 妇科 遗传学 生物 基因 环境卫生
作者
Victoria Sopik,Catherine M. Phelan,Cezary Cybulski,Steven A. Narod
出处
期刊:Clinical Genetics [Wiley]
卷期号:87 (5): 411-418 被引量:75
标识
DOI:10.1111/cge.12497
摘要

Women who carry a BRCA1 or BRCA2 mutation are at high risk of breast and ovarian cancer, and may be at moderately increased risk of other cancer types. This review examines studies to date that have evaluated the risk of BRCA1 and BRCA2 mutations for colorectal cancer. Accurate knowledge of colorectal cancer risk in BRCA1 /2 carriers is important, because colonoscopy screening can prevent colorectal cancer through the removal of adenomatous polyps. Most studies that have identified an increased risk for colorectal cancer in BRCA1 /2 mutation carriers were in high‐risk cancer families, while studies that found no association were conducted in specific populations and involved the analysis of founder mutations. A recent prospective study of 7015 women with a BRCA1 or BRCA2 mutation identified significant fivefold increased risk of colorectal cancer among BRCA1 mutation carriers younger than 50 years [standardized incidence ratio ( SIR ): 4.8; 95% CI : 2.2–9], but not in women with a BRCA2 mutation or in older women. Based on this evidence, women with BRCA1 mutations should be counseled about their increased risk for early‐onset colorectal cancer, and offered colonoscopy at 3‐ to 5‐year intervals between the ages of 40 and 50 years, and should follow population guidelines thereafter.
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