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BRCA1 或 BRCA2 基因突变女性的癌症家族史和癌症风险。

Family history of cancer and cancer risks in women with BRCA1 or BRCA2 mutations.

机构信息

Women's College Research Institute, Toronto, ON, Canada.

出版信息

J Natl Cancer Inst. 2010 Dec 15;102(24):1874-8. doi: 10.1093/jnci/djq443. Epub 2010 Nov 23.

Abstract

Women who carry a deleterious mutation in BRCA1 or BRCA2 have high lifetime risks of breast and ovarian cancers. However, the influence of a family history of these cancers on these risks in women with BRCA mutations is unclear. We calculated cancer incidence rates for a multinational cohort comprising 3011 women with BRCA1 or BRCA2 mutations who were followed up for a mean of 3.9 years, during which time 243 incident breast or ovarian cancers were recorded. The 10-year cumulative risks of breast cancer were 18.1% (95% confidence interval [CI] = 13.3% to 22.8%) for women with a BRCA1 mutation and 15.2% (95% CI = 9.1% to 21.2%) for women with a BRCA2 mutation. Among women with a BRCA1 mutation, the risk of breast cancer increased by 1.2-fold for each first-degree relative with breast cancer before age 50 years (hazard ratio [HR] = 1.21; 95% confidence interval [CI] = 0.94 to 1.57) and the risk of ovarian cancer increased by 1.6 fold for each first- or second-degree relative with ovarian cancer (HR = 1.61; 95% CI = 1.21 to 2.14). Among women with a BRCA2 mutation, the risk of breast cancer increased by 1.7-fold for each first-degree relative younger than 50 years with breast cancer (HR = 1.67; 95% CI = 1.04 to 2.07).

摘要

携带有害 BRCA1 或 BRCA2 突变的女性具有较高的乳腺癌和卵巢癌终生风险。然而,BRCA 突变女性中家族史对这些风险的影响尚不清楚。我们计算了一个由 3011 名携带 BRCA1 或 BRCA2 突变的女性组成的跨国队列的癌症发病率,这些女性平均随访 3.9 年,在此期间记录了 243 例乳腺癌或卵巢癌的发病情况。BRCA1 突变女性的 10 年乳腺癌累积风险为 18.1%(95%置信区间[CI] = 13.3%至 22.8%),BRCA2 突变女性为 15.2%(95%CI = 9.1%至 21.2%)。在 BRCA1 突变女性中,每有一位 50 岁前患有乳腺癌的一级亲属,乳腺癌风险增加 1.2 倍(风险比[HR] = 1.21;95%置信区间[CI] = 0.94 至 1.57),每有一位一级或二级亲属患有卵巢癌,卵巢癌风险增加 1.6 倍(HR = 1.61;95%CI = 1.21 至 2.14)。在 BRCA2 突变女性中,每有一位 50 岁前患有乳腺癌的一级亲属,乳腺癌风险增加 1.7 倍(HR = 1.67;95%CI = 1.04 至 2.07)。

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