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家族前列腺癌和乳腺癌病史与多基因风险评分相结合,可识别出 75 岁前死于前列腺癌风险最高的男性。

Family History of Prostate and Breast Cancer Integrated with a Polygenic Risk Score Identifies Men at Highest Risk of Dying from Prostate Cancer before Age 75 Years.

机构信息

Urology Division, Department of Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts.

Department of Epidemiology, Harvard T.H. Chan School of Public Health, Boston, Massachusetts.

出版信息

Clin Cancer Res. 2022 Nov 14;28(22):4926-4933. doi: 10.1158/1078-0432.CCR-22-1723.

Abstract

PURPOSE

Family history of prostate cancer is one of the few universally accepted risk factors for prostate cancer. How much an assessment of inherited polygenic risk for prostate cancer adds to lifetime risk stratification beyond family history is unknown.

EXPERIMENTAL DESIGN

We followed 10,120 men in the Health Professionals Follow-up Study with existing genotype data for risk of prostate cancer and prostate cancer-specific death. We assessed to what extent family history of prostate or breast cancer, combined with a validated polygenic risk score (PRS) including 269 prostate cancer risk variants, identifies men at risk of prostate cancer and prostate cancer death across the age span.

RESULTS

During 20 years of follow-up, 1,915 prostate cancer and 166 fatal prostate cancer events were observed. Men in the top PRS quartile with a family history of prostate or breast cancer had the highest rate of both prostate cancer and prostate cancer-specific death. Compared with men at lowest genetic risk (bottom PRS quartile and no family history), the HR was 6.95 [95% confidence interval (CI), 5.57-8.66] for prostate cancer and 4.84 (95% CI, 2.59-9.03) for prostate cancer death. Men in the two upper PRS quartiles (50%-100%) or with a family history of prostate or breast cancer (61.8% of the population) accounted for 97.5% of prostate cancer deaths by age 75 years.

CONCLUSIONS

Our study shows that prostate cancer risk stratification on the basis of family history and inherited polygenic risk can identify men at highest risk of dying from prostate cancer before age 75 years.

摘要

目的

前列腺癌家族史是少数被广泛认可的前列腺癌风险因素之一。评估前列腺癌遗传多基因风险在多大程度上可以补充家族史对终生风险分层的作用尚不清楚。

实验设计

我们对参加“卫生专业人员随访研究”的 10120 名男性进行了随访,这些男性有前列腺癌风险和前列腺癌特异性死亡的现有基因型数据。我们评估了家族前列腺癌或乳腺癌史,结合包括 269 个前列腺癌风险变异体在内的验证过的多基因风险评分(PRS),在多大程度上可以识别出处于前列腺癌和前列腺癌死亡风险的男性,以及跨越年龄跨度的男性。

结果

在 20 年的随访期间,观察到 1915 例前列腺癌和 166 例致命性前列腺癌事件。有家族前列腺癌或乳腺癌史且PRS 位于四分位最高位的男性,前列腺癌和前列腺癌特异性死亡的发生率最高。与处于最低遗传风险(PRS 最低四分位且无家族史)的男性相比,前列腺癌的 HR 为 6.95(95%CI,5.57-8.66),前列腺癌死亡的 HR 为 4.84(95%CI,2.59-9.03)。在两个PRS 四分位较高(50%-100%)或有家族前列腺癌或乳腺癌史(占人群的 61.8%)的男性中,97.5%的前列腺癌死亡发生在 75 岁之前。

结论

我们的研究表明,基于家族史和遗传多基因风险的前列腺癌风险分层,可以识别出在 75 岁之前死于前列腺癌的风险最高的男性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/082e/9660541/403d29465ce5/4926fig1.jpg

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