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Early PSA level decline is an independent predictor of biochemical and clinical control for salvage postprostatectomy radiotherapy.

Authors :
Blanchard P
Bakkour M
De Crevoisier R
Levy A
Baumert H
Patard JJ
Wibault P
Fizazi K
Bossi A
Source :
Urologic oncology [Urol Oncol] 2015 Mar; Vol. 33 (3), pp. 108.e15-20. Date of Electronic Publication: 2014 Aug 28.
Publication Year :
2015

Abstract

Background: To improve the early detection of responders to salvage external beam radiotherapy (RT) after radical prostatectomy (RP).<br />Methods: Between 2002 and 2007, in a single institution, 136 consecutive patients received salvage RT to a dose of 66 Gy without androgen-deprivation therapy after RP for a rising prostate-specific antigen (PSA) level. PSA measurements were systematically performed before RT (PSART), at the fifth week of RT (PSA5), and in the follow-up at least twice a year (every 6 mo). The PSA level decline during RT was expressed as PSA ratio (PSA5/PSART). Two different definitions of biochemical failure after salvage RT were considered: PSA level>0.4 ng/ml and PSA>PSA nadir post-RT +0.4 ng/ml. Statistical analyses included univariate and multivariate Cox regression models.<br />Results: The median follow-up was 60 months. The 5-year freedom from biochemical and clinical failure rates were 57% (95% CI: 48%-66%) and 92% (95% CI: 87%-97%), respectively. The mean PSA5 was 0.61 ng/ml (range: 0-7) and the mean PSA ratio was 0.67 (0-1.7). A PSA ratio<1 was a significant prognostic factor in multivariate analysis for both definitions of biochemical failure (P = 0.01 for both) and for clinical failure (P = 0.005).<br />Conclusions: For patients undergoing salvage RT after RP for a rising PSA level, the absence of PSA level decline during RT is predictive of biochemical and clinical failure and may be used to rapidly identify poor responders.<br /> (Copyright © 2015 Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1873-2496
Volume :
33
Issue :
3
Database :
MEDLINE
Journal :
Urologic oncology
Publication Type :
Academic Journal
Accession number :
25176583
Full Text :
https://doi.org/10.1016/j.urolonc.2014.07.020