Publication: Prostate-specific antigen level at the time of salvage therapy after radical prostatectomy for prostate cancer and the risk of death
Program
KU-Authors
KU Authors
Co-Authors
Chen, Ming-Hui
Wu, Jing
Huland, Hartwig
Graefen, Markus
Mohamad, Osama
Cowan, Janet E.
Feng, Felix Y.
Carroll, Peter R.
D'Amico, Anthony V.
Advisor
Publication Date
2023
Language
English
Type
Journal Article
Journal Title
Journal ISSN
Volume Title
Abstract
Purpose: Both the performance characteristics of prostate-specific membrane antigen positron emission tomography and insurance approval improves with increasing prostate-specific antigen (PSA) level causing some physicians to delay post-radical prostatectomy salvage radiation therapy (sRT) after PSA failure. Yet, it is unknown for men with at most one high-risk factor (ie, pT3/4 or prostatectomy [p] Gleason score 8-10) whether a PSA level exists above which initiating sRT is associated with increased all-cause mortality (ACM)-risk and was investigated. Methods: Using a multinational database of 25,551 patients with pT2-4N0 or NXM0 prostate cancer, multivariable Cox regression analysis evaluated whether an association with a significant increase in ACM-risk existed when sRT was delivered above a prespecified PSA level beginning at 0.10 ng/mL and in 0.05 increments up to 0.50 ng/mL versus at or below that level. The model was adjusted for age at and year of radical prostatectomy, established prostate cancer prognostic factors, institution, and the time-dependent use of androgen deprivation therapy. Results: After a median follow-up of 6.00 years, patients who received sRT at a PSA level >0.25 ng/mL had a significantly higher ACM-risk (AHR, 1.49; 95% CI, 1.11 to 2.00; P = .008) compared with men who received sRT when the PSA was ≤0.25 mg/mL. This elevated ACM-risk remained significant for all PSA cutpoints up to 0.50 ng/mL but was not significant at PSA cutpoint values below 0.25 ng/mL. Conclusion: Among patients with at most one high-risk factor, initiating sRT above a PSA level of 0.25 ng/mL was associated with increased ACM-risk.
Description
Source:
Journal of Clinical Oncology
Publisher:
American Society of Clinical Oncology
Keywords:
Subject
Neoplasms, Forensic oncology