Identifying Patients at Risk of Early Lethal Prostate Cancer by Integrating Family History, Polygenic Risk Score, Rare Variants in DNA Repair Genes, and Lifestyle Factors.

IF 8.3 1区 医学 Q1 ONCOLOGY
Zhizhu Zhang, Yiwen Zhang, Konrad H Stopsack, Adam S Kibel, Edward L Giovannucci, Kathryn L Penney, Anqi Wang, Joseph Vijai, Philip W Kantoff, Mark M Pomerantz, Kenneth Offit, Lorelei A Mucci, Anna Plym
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Abstract

Background and objective: In men with prostate cancer, one-third of deaths occur before the age of 75 yr. There remains a need to characterize heritable and environmental risk factors for these early deaths. This study aims to improve risk stratification for early lethal outcomes among prostate cancer patients with genetic factors beyond family history and with modifiable factors.

Methods: This study included 966 prostate cancer patients, enriched for high-risk localized disease and with germline genetic data, in two prospective cohorts. Three genetic factors (family history of prostate cancer, polygenic risk score [PRS] in the top 20%, and rare variants in DNA repair genes) and a lifestyle score were examined for their association with early lethal (metastases/prostate cancer death before the age of 75 yr) compared with nonlethal cases using logistic regression and by calculating 10-yr lethal disease risks.

Key findings and limitations: In total, 289 lethal, including 77 early lethal, cases were observed (median age at the end follow-up: 84.3 yr). Early lethal cases had higher percentages of men with a family history (23% vs 15%), a high PRS (47% vs 36%), and rare variants (14% vs 7.8%). Having two or more genetic factors was strongly associated with increased odds of early lethal disease (odds ratio [OR], 3.5; 95% confidence interval [CI], 1.8-7.0) and linked to higher 10-yr lethal disease risks in high-risk localized patients diagnosed before the age of 75 yr. Healthy men with none of the genetic factors had the lowest odds of early lethal disease (OR, 0.3: 95% CI, 0.1-0.7), compared with unhealthy men with any genetic factor. The pattterns were similar for early fatal disease. The study had limited data for more detailed analyses.

Conclusions and clinical implications: The combination of family history with rare variants, a PRS, and lifestyle factors may improve the identification of prostate cancer patients at risk of early lethal and fatal disease.

通过整合家族史、多基因风险评分、DNA修复基因罕见变异和生活方式因素来识别早期致死性前列腺癌患者
背景和目的:在前列腺癌男性患者中,三分之一的死亡发生在75岁之前。仍有必要确定这些早期死亡的遗传和环境风险因素。本研究旨在改善具有家族病史以外遗传因素和可改变因素的前列腺癌患者早期致死结果的风险分层。方法:本研究纳入两组前瞻性队列,966例前列腺癌患者,富集了高风险局部疾病和生殖系遗传数据。通过逻辑回归和计算10年致死疾病风险,研究了三个遗传因素(前列腺癌家族史、前20%的多基因风险评分[PRS]和DNA修复基因的罕见变异)和生活方式评分与非致死病例(75岁前转移/前列腺癌死亡)的相关性。主要发现和局限性:共观察到289例死亡病例,包括77例早期死亡病例(随访结束时中位年龄:84.3岁)。早期致死病例中有家族史的男性比例较高(23%比15%),高PRS(47%比36%)和罕见变异(14%比7.8%)。拥有两种或两种以上的遗传因素与早期致死疾病的几率增加密切相关(优势比[or], 3.5;95%可信区间[CI], 1.8-7.0),并与75岁前诊断的高风险局部患者10年致死疾病风险较高相关。与有任何遗传因素的不健康男性相比,没有任何遗传因素的健康男性患早期致死疾病的几率最低(OR, 0.3: 95% CI, 0.1-0.7)。这种模式与早期致命性疾病相似。这项研究的数据有限,无法进行更详细的分析。结论和临床意义:结合罕见变异家族史、PRS和生活方式因素可以提高前列腺癌患者早期致死和致命疾病风险的识别。
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来源期刊
CiteScore
15.50
自引率
2.40%
发文量
128
审稿时长
20 days
期刊介绍: Journal Name: European Urology Oncology Affiliation: Official Journal of the European Association of Urology Focus: First official publication of the EAU fully devoted to the study of genitourinary malignancies Aims to deliver high-quality research Content: Includes original articles, opinion piece editorials, and invited reviews Covers clinical, basic, and translational research Publication Frequency: Six times a year in electronic format
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