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A Contemporary Prostate Biopsy Risk Calculator Based on Multiple Heterogeneous Cohorts

医学 前列腺癌 前列腺活检 活检 前列腺 置信区间 逻辑回归 直肠检查 前列腺特异性抗原 前列腺切除术 接收机工作特性 肿瘤科 内科学 放射科 癌症
作者
Donna P. Ankerst,J. Straubinger,Katharina Selig,Lourdes Guerrios‐Rivera,Amanda M. De Hoedt,Javier Hernández,Michael A. Liss,Robin J. Leach,Stephen J. Freedland,Michael W. Kattan,Robert K. Nam,Alexander Haese,Francesco Montorsi,Stephen A. Boorjian,Matthew R. Cooperberg,Cédric Poyet,Emily Vertosick,Andrew Vickers
出处
期刊:European Urology [Elsevier BV]
卷期号:74 (2): 197-203 被引量:95
标识
DOI:10.1016/j.eururo.2018.05.003
摘要

Prostate cancer prediction tools provide quantitative guidance for doctor-patient decision-making regarding biopsy. The widely used online Prostate Cancer Prevention Trial Risk Calculator (PCPTRC) utilized data from the 1990s based on six-core biopsies and outdated grading systems. We prospectively gathered data from men undergoing prostate biopsy in multiple diverse North American and European institutions participating in the Prostate Biopsy Collaborative Group (PBCG) in order to build a state-of-the-art risk prediction tool. We obtained data from 15 611 men undergoing 16 369 prostate biopsies during 2006–2017 at eight North American institutions for model-building and three European institutions for validation. We used multinomial logistic regression to estimate the risks of high-grade prostate cancer (Gleason score ≥7) on biopsy based on clinical characteristics, including age, prostate-specific antigen, digital rectal exam, African ancestry, first-degree family history, and prior negative biopsy. We compared the PBCG model to the PCPTRC using internal cross-validation and external validation on the European cohorts. Cross-validation on the North American cohorts (5992 biopsies) yielded the PBCG model area under the receiver operating characteristic curve (AUC) as 75.5% (95% confidence interval: 74.2–76.8), a small improvement over the AUC of 72.3% (70.9–73.7) for the PCPTRC (p < 0.0001). However, calibration and clinical net benefit were far superior for the PBCG model. Using a risk threshold of 10%, clinical use of the PBCG model would lead to the equivalent of 25 fewer biopsies per 1000 patients without missing any high-grade cancers. Results were similar on external validation on 10 377 European biopsies. The PBCG model should be used in place of the PCPTRC for prediction of prostate biopsy outcome. A contemporary risk tool for outcomes on prostate biopsy based on the routine clinical risk factors is now available for informed decision-making.

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