“…9 Similarly, CAPRA does not account for the presence of Gleason pattern 5 (GP-5), which even as a tertiary pattern is an established independent adverse prognostic factor in PC. [15][16][17] Although these limitations would not be expected to significantly impact the discriminatory ability of the CAPRA instrument to predict outcomes in surgical cohorts, which generally consist of limited numbers of patients with high-risk GS or GP-5, CAPRA is less likely to accurately discriminate risk in populations treated with EBRT, which typically have a higher prevalence of high-risk GSs. 9,11,13,14,18 The insensitivity of CAPRA to such risk differences between RP and EBRT patients may, therefore, underestimate risk in EBRT patients, and has the potential to confound results of observational studies that use CAPRA for risk adjustment between patients treated with EBRT and RP.…”