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Updated: Feb 28, 2026

A Bioluminescent and Fluorescent Orthotopic Syngeneic Murine Model of Androgen-dependent and Castration-resistant Prostate Cancer
Published on: March 6, 2018
Prostate-specific antigen velocity as a predictor of survival outcomes in patients with prostate cancer: a
Feilun Cui1,2, Yueshi Zhang3, Ziyan Liu3
1Department of Urology, The Fourth Affiliated Hospital of Jiangsu University, Zhenjiang, China.
Background:
Prostate-specific antigen velocity (PSAV) has emerged as a promising biomarker for predicting survival outcomes in prostate cancer patients.
Objectives:
To assess the association between PSAV and both all-cause mortality and prostate cancer-specific mortality (PCSM) in men diagnosed with prostate cancer by conducting a meta-analysis.
Methods:
A comprehensive search of electronic medical databases, including PubMed, Web of Science, and Embase, was conducted to identify relevant studies published up to March 1, 2025. Studies reporting adjusted hazard ratios (HR) with 95% confidence intervals (CI) for survival outcomes in prostate cancer patients, based on categorical analyses of PSAV, were included. Pooled HRs with 95% CI was calculated using random-effects models to account for clinical heterogeneity across studies.
Result:
Eleven studies involving 3,713 prostate cancer patients were identified and analyzed. The meta-analysis revealed that elevated PSAV was associated with a higher risk of both all-cause mortality (HR 1.96; 95% CI 1.33-2.88) and PCSM (HR 5.38; 95% CI 2.76-10.51). In stratified analyses, the pooled HR for all-cause mortality was 1.91 (95% CI 1.43-2.55) among patients with localized prostate cancer, compared to 1.26 (95% CI 0.41-3.84) in those with metastatic disease.
Conclusions:
Elevated PSAV is a significant predictor of all-cause mortality and PCSM in prostate cancer patients. Measuring PSAV has the potential to improve the prediction of survival outcomes in this population. However, further research is needed to standardize PSAV measurement and validate its predictive value across diverse patient groups. Systematic review registration.
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