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  • Prospective Multi-Instituti...
    NAM, Robert K; KATTAN, Michael W; BELL, David; STANIMIROVIC, Aleksandra; VENKATESWARAN, Vasundara; DIAMANDIS, Eleftherios P; CHANGHONG YU; LOBLAW, D. Andrew; NAROD, Steven A; CHIN, Joseph L; TRACHTENBERG, John; SINGAL, Rajiv; RENDON, Ricardo; KLOTZ, Laurence H; SUGAR, Linda; SHERMAN, Christopher; IZAWA, Jonathan

    Journal of clinical oncology, 08/2011, Letnik: 29, Številka: 22
    Journal Article

    Prostate cancer risk calculators incorporate many factors to evaluate an individual's risk for prostate cancer. We validated two common North American-based, prostate cancer risk calculators. We conducted a prospective, multi-institutional study of 2,130 patients who underwent a prostate biopsy for prostate cancer detection from five centers. We evaluated the performance of the Sunnybrook nomogram-based prostate cancer risk calculator (SRC) and the Prostate Cancer Prevention Trial (PCPT) -based risk calculator (PRC) to predict the presence of any cancer and high-grade cancer. We examined discrimination, calibration, and decision curve analysis techniques to evaluate the prediction models. Of the 2,130 patients, 867 men (40.7%) were found to have cancer, and 1,263 (59.3%) did not have cancer. Of the patients with cancer, 403 (46.5%) had a Gleason score of 7 or more. The area under the concentration-time curve (AUC) for the SRC was 0.67 (95% CI, 0.65 to 0.69); the AUC for the PRC was 0.61 (95% CI, 0.59 to 0.64). The AUC was higher for predicting aggressive disease from the SRC (0.72; 95% CI, 0.70 to 0.75) compared with that from the PRC (0.67; 95% CI, 0.64 to 0.70). Decision curve analyses showed that the SRC performed better than the PRC for risk thresholds of more than 30% for any cancer and more than 15% for aggressive cancer. The SRC performed better than the PRC, but neither one added clinical benefit for risk thresholds of less than 30%. Further research is needed to improve the AUCs of the risk calculators, particularly for higher-grade cancer.