Performance characteristics of prostate-specific antigen in patients undergoing radical prostatectomy - Abstract

OBJECTIVE:To assess the performance characteristics of prostate-specific antigen (PSA) for predicting the volume of total or high-grade cancer in men undergoing radical prostatectomy.

It is known that the performance characteristics of PSA are improved for predicting the presence of high-grade prostate cancer.

METHODS:We identified 1459 patients from the Stanford Radical Prostatectomy Database with clinical Stage T1c (n = 783) and T2 (n = 676) disease who underwent surgery from 1988 to 2003 with detailed morphometric mapping. We generated receiver operating characteristic curves for PSA levels according to the total and high-grade (Gleason score 4 or 5) cancer volume and compared the areas under the curve (AUC) for the various total and high-grade cancer volumes.

RESULTS:For patients with Stage T1c disease, the AUC for the PSA ROC curve increased in a stepwise fashion as both the total cancer volume and the high-grade cancer volume increased. Significant differences between the AUCs for low and high volumes of total and high-grade disease were observed. For T2 disease, the AUCs for predicting high-grade cancer volume were generally greater than the corresponding AUCs for T1c disease, although no incremental increase was observed.

CONCLUSION: In patients with Stage T1c disease, in whom the PSA level was the driving force for biopsy, the PSA performance improved in a stepwise fashion with greater total and high-grade cancer volumes as evidenced by improved ROC. Previous studies have shown that PSA performs better for detecting the presence of high-grade disease. We have shown that PSA performs better in predicting greater volumes of high-grade disease in radical prostatectomy specimens.

Written by:
Liu JJ, Ferrari M, Nolley R, Brooks JD, Presti JC Jr. Are you the author?
Department of Urology, Stanford University School of Medicine, Stanford, California.

Reference: Urology. 2012 Jun;79(6):1336-9.
doi: 10.1016/j.urology.2012.02.036

PubMed Abstract
PMID: 22516358

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