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Impact of preoperative risk on metastatic progression and cancer-specific mortality in patients with adverse pathology at radical prostatectomy.

Authors :
Boehm K
Leyh-Bannurah SR
Rosenbaum C
Brandi LS
Budäus L
Graefen M
Huland H
Haferkamp A
Tilki D
Source :
BJU international [BJU Int] 2017 Nov; Vol. 120 (5), pp. 666-672. Date of Electronic Publication: 2017 May 29.
Publication Year :
2017

Abstract

Objective: To evaluate the impact of preoperative risk category on metastatic disease and prostate cancer-specific mortality (CSM) in patients with prostate cancer (PCa) with adverse pathology at radical prostatectomy (RP).<br />Patients and Methods: The records of 6 943 patients who underwent RP at a European tertiary centre were analysed. Biochemical recurrence (BCR), metastatic disease and CSM were assessed for patients with adverse pathology at RP, and stratified according to preoperative low- vs intermediate-/high-risk PCa groups. Kaplan-Meier, cumulative incidence, Cox regression and competing risk regression analyses were performed.<br />Results: In patients with extracapsular extension, the metastatic disease rate was 1.6% vs 8% (P < 0.001) and the CSM rate was 2% vs 5% (P = 0.041) for low vs intermediate-/high-risk patients, respectively, at 10 years. In patients with pathological Gleason score ≥3+4, the metastatic disease rate was 3.0% vs 12% (P < 0.001) and the CSM rate was 3% vs 8%, respectively (P < 0.001). In patients with positive surgical margins (PSMs), the metastatic disease rate was 2.9% vs 15% (P < 0.001) and the CSM rate was 4% vs 10%, respectively (P = 0.0001). Low-risk status was a predictive factor for metastatic disease in patients with pathological Gleason score ≥3+4 (hazard ratio [HR] 0.51), pathological Gleason score ≥4+3 (HR 0.41) and PSMs (HR 0.46) and was a predictive factor for CSM risk in patients with pathological Gleason score ≥3+4 (HR 0.62).<br />Conclusions: Patients with low-risk PCa were at significantly lower risk of metastatic disease and CSM than their intermediate-/high-risk counterparts, when adverse pathological features were identified at RP. This should be emphasized in the decision-making process after RP.<br /> (© 2017 The Authors BJU International © 2017 BJU International Published by John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1464-410X
Volume :
120
Issue :
5
Database :
MEDLINE
Journal :
BJU international
Publication Type :
Academic Journal
Accession number :
28437038
Full Text :
https://doi.org/10.1111/bju.13887