Assessing the Clinical Utility of Published Prostate Cancer Polygenic Risk Scores in a Large Biobank Data Set

被引:0
作者
Vince Jr, Randy A. [1 ]
Sun, Helen [1 ]
Singhal, Udit [2 ]
Schumacher, Fredrick R. [3 ]
Trapl, Erika [3 ]
Rose, Johnie [3 ]
Cullen, Jennifer [3 ]
Zaorsky, Nicholas [4 ]
Shoag, Jonathan [1 ]
Hartman, Holly [3 ]
Jia, Angela Y. [4 ]
Spratt, Daniel E. [4 ]
Fritsche, Lars G. [5 ]
Morgan, Todd M. [2 ]
机构
[1] Case Western Reserve Univ, Univ Hosp Seidman, Dept Urol, Canc Ctr, Cleveland, OH USA
[2] Univ Michigan, Dept Urol, Michigan Med, Ann Arbor, MI USA
[3] Case Western Reserve Univ, Dept Populat & Quantitat Hlth Sci, Cleveland, OH USA
[4] Case Western Reserve Univ, Univ Hosp Seidman, Dept Radiat Oncol, Canc Ctr, Cleveland, OH USA
[5] Univ Michigan, Ctr Stat Genet, Sch Publ Hlth, Dept Biostat, Ann Arbor, MI USA
来源
EUROPEAN UROLOGY ONCOLOGY | 2025年 / 8卷 / 01期
关键词
Prostate cancer; Polygenic risk score; Screening; Risk stratification; GENOME-WIDE ASSOCIATION; SUSCEPTIBILITY; PREDICTION; HERITABILITY; CONSORTIUM; VARIANTS; TRAITS; BREAST;
D O I
10.1016/j.euo.2024.04.017
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background and objective: Polygenic risk scores (PRSs) have been developed to identify men with the highest risk of prostate cancer. Our aim was to compare the performance of 16 PRSs in identifying men at risk of developing prostate cancer and then to evaluate the performance of the top-performing PRSs in differentiating individuals at risk of aggressive prostate cancer. Methods: For this case-control study we downloaded 16 published PRSs from the Polygenic Score Catalog on May 28, 2021 and applied them to Michigan Genomics Initiative (MGI) patients. Cases were matched to the Michigan Urological Surgery Improvement Collaborative (MUSIC) registry to obtain granular clinical and pathological data. MGI prospectively enrolls patients undergoing surgery at the University of Michigan, and MUSIC is a multi-institutional registry that prospectively tracks demographic, treatment, and clinical variables. The predictive performance of each PRS was evaluated using the area under the covariate-adjusted receiver operating characteristic curve (aAUC), and the association between PRS and disease aggressiveness according to prostate biopsy data was measured using logistic regression. Key findings and limitations: We included 18 050 patients in the analysis, of whom 15 310 were control subjects and 2740 were prostate cancer cases. The median age was 66.1 yr (interquartile range 59.9-71.6) for cases and 56.6 yr (interquartile range 42.6-66.7) for control subjects. The PRS performance in predicting the risk of developing prostate cancer according to aAUC ranged from 0.51 (95% confidence interval 0.51-0.53) to 0.67 (95% confidence interval 0.66-0.68). By contrast, there was no association between PRS and disease aggressiveness. Conclusions and clinical implications: Prostate cancer PRSs have modest real-world performance in identifying patients at higher risk of developing prostate cancer; however, they are limited in distinguishing patients with indolent versus aggressive disease. Patient summary: Risk scores using data for multiple genes (called polygenic risk scores) can identify men at higher risk of developing prostate cancer. However, these scores need to be refined to be able to identify men with the highest risk for clinically significant prostate cancer. (c) 2024 European Association of Urology. Published by Elsevier B.V. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
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页码:47 / 55
页数:9
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