A contemporary prostate biopsy risk calculator based on multiple heterogeneous cohorts Journal Article


Authors: Ankerst, D. P.; Straubinger, J.; Selig, K.; Guerrios, L.; De Hoedt, A.; Hernandez, J.; Liss, M. A.; Leach, R. J.; Freedland, S. J.; Kattan, M. W.; Nam, R.; Haese, A.; Montorsi, F.; Boorjian, S. A.; Cooperberg, M. R.; Poyet, C.; Vertosick, E.; Vickers, A. J.
Article Title: A contemporary prostate biopsy risk calculator based on multiple heterogeneous cohorts
Abstract: A North American multicohort-based risk tool for predicting prostate cancer outcomes on biopsy has been developed and outperformed a leading North American risk tool in validation. It is now available online for patients and their providers. Background: 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Prostate Cancer Prevention Trial Risk Calculator (PCPTRC) utilized data from the 1990s based on six-core biopsies and outdated grading systems. Objective: 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. Design, setting, and participants: 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. Outcome measurements and statistical analysis: 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. Results and limitations: 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. Conclusions: The PBCG model should be used in place of the PCPTRC for prediction of prostate biopsy outcome. Patient summary: A contemporary risk tool for outcomes on prostate biopsy based on the routine clinical risk factors is now available for informed decision-making. © 2018 European Association of Urology
Keywords: adult; aged; major clinical study; clinical feature; cancer grading; prostate specific antigen; prediction; risk assessment; prostate cancer; gleason score; prostate-specific antigen; family history; prostate biopsy; digital rectal examination; african; clinical assessment tool; risk prediction; ancestry group; human; male; priority journal; article; digital rectal exam; high-grade disease; prostate biopsy risk calculator
Journal Title: European Urology
Volume: 74
Issue: 2
ISSN: 0302-2838
Publisher: Elsevier Science, Inc.  
Date Published: 2018-08-01
Start Page: 197
End Page: 203
Language: English
DOI: 10.1016/j.eururo.2018.05.003
PROVIDER: scopus
PUBMED: 29778349
PMCID: PMC6082177
DOI/URL:
Notes: Article -- Export Date: 1 August 2018 -- Source: Scopus
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  1. Andrew J Vickers
    880 Vickers
  2. Emily Vertosick
    134 Vertosick