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携带BRCA1或BRCA2基因突变的中国女性患乳腺癌的风险。

Breast cancer risk in Chinese women with BRCA1 or BRCA2 mutations.

作者信息

Yao Lu, Sun Jie, Zhang Juan, He Yingjian, Ouyang Tao, Li Jinfeng, Wang Tianfeng, Fan Zhaoqing, Fan Tie, Lin Benyao, Xie Yuntao

机构信息

Key Laboratory of Carcinogenesis and Translational Research (Ministry of Education/Beijing), Breast Center, Peking University Cancer Hospital & Institute, Beijing, 100142, People's Republic of China.

出版信息

Breast Cancer Res Treat. 2016 Apr;156(3):441-445. doi: 10.1007/s10549-016-3766-3. Epub 2016 Mar 31.

Abstract

BRCA1/2 mutations represent approximately 5 % of unselected Chinese women with breast cancer. However, the breast cancer risk of Chinese women with BRCA1/2 mutations is unknown. Therefore, the aim of this study was to estimate the age-specific cumulative risk of breast cancer in Chinese women who carry a BRCA1 or BRCA2 mutation. Our study included 1816 unselected Chinese women with breast cancer and 5549 female first-degree relatives of these probands. All probands were screened for BRCA1/2 mutation. The age-specific cumulative risks of BRCA1/2 carriers were estimated using the kin-cohort study by comparing the history of breast cancer in first-degree female relatives of BRCA1/2 carriers and non-carriers. Among the 1816 probands, 125 BRCA1/2 pathogenic mutations were identified (70 in the BRCA1 gene and 55 in the BRCA2 gene). The incidence of breast cancer in the first-degree female relatives of BRCA1/2 mutation carriers was significantly higher (3.7-fold and 4.4-fold for BRCA1 and BRCA2 mutation carriers, respectively) than in non-carriers. The estimated cumulative risks of breast cancer by age 70 years were 37.9 % [95 % confidence interval (CI) 24.1-54.4 %] for BRCA1 mutation carriers and 36.5 % (95 % CI 26.7-51.8 %) for BRCA2 mutation carriers, respectively. Our study suggests that the breast cancer risk of Chinese women with BRCA1/2 mutations appears to be relatively high by the age of 70. Therefore, genetic counseling, enhanced surveillance, and individual preventive strategies should be provided for Chinese women who carry a BRCA1/2 mutation.

摘要

BRCA1/2基因突变在未经选择的中国乳腺癌女性中约占5%。然而,携带BRCA1/2基因突变的中国女性患乳腺癌的风险尚不清楚。因此,本研究的目的是估计携带BRCA1或BRCA2基因突变的中国女性特定年龄的乳腺癌累积风险。我们的研究纳入了1816名未经选择的中国乳腺癌女性以及这些先证者的5549名女性一级亲属。对所有先证者进行BRCA1/2基因突变筛查。通过比较BRCA1/2基因携带者和非携带者的女性一级亲属的乳腺癌病史,利用亲属队列研究估计BRCA1/2基因携带者特定年龄的累积风险。在1816名先证者中,鉴定出125个BRCA1/2致病突变(BRCA1基因70个,BRCA2基因55个)。BRCA1/2基因突变携带者的女性一级亲属的乳腺癌发病率显著高于非携带者(BRCA1和BRCA2基因突变携带者分别高3.7倍和4.4倍)。BRCA1基因突变携带者到70岁时估计的乳腺癌累积风险为37.9%[95%置信区间(CI)24.1 - 54.4%],BRCA2基因突变携带者为36.5%(95%CI 26.7 - 51.8%)。我们的研究表明,携带BRCA1/2基因突变的中国女性到70岁时患乳腺癌的风险似乎相对较高。因此,应为携带BRCA1/2基因突变的中国女性提供遗传咨询、加强监测和个体化预防策略。

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