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Int. J. Radiat. Oncol. Biol. Phys. · Jul 2012
High-dose adjuvant radiotherapy after radical prostatectomy with or without androgen deprivation therapy.
- Piet Ost, Cesare Cozzarini, Gert De Meerleer, Claudio Fiorino, Bruno De Potter, Alberto Briganti, Evi V T Nagler, Francesco Montorsi, Valérie Fonteyne, and Nadia Di Muzio.
- Department of Radiotherapy, Ghent University Hospital, Ghent, Belgium. piet.ost@ugent.be
- Int. J. Radiat. Oncol. Biol. Phys. 2012 Jul 1; 83 (3): 960-5.
PurposeTo retrospectively evaluate the outcome and toxicity in patients receiving high-dose (>69 Gy) adjuvant radiotherapy (HD-ART) and the impact of androgen deprivation therapy (ADT).Methods And MaterialsBetween 1999 and 2008, 225 node-negative patients were referred for HD-ART with or without ADT to two large academic institutions. Indications for HD-ART were extracapsular extension, seminal vesicle invasion (SVI), and/or positive surgical margins at radical prostatectomy (RP). A dose of at least 69.1 Gy was prescribed to the prostate bed and seminal vesicle bed. The ADT consisted of a luteinizing hormone-releasing hormone analog. The duration and indication of ADT was left at the discretion of the treating physician. The effect of HD-ART and ADT on biochemical (bRFS) and clinical (cRFS) relapse-free survival was examined through univariate and multivariate analysis, with correction for known patient- and treatment-related variables. Interaction terms were introduced to evaluate effect modification.ResultsAfter a median follow-up time of 5 years, the 7-year bRFS and cRFS were 84% and 88%, respectively. On multivariate analysis, the addition of ADT was independently associated with an improved bRFS (hazard ratio [HR] 0.4, p = 0.02) and cRFS (HR 0.2, p = 0.008). Higher Gleason scores and SVI were associated with decreased bRFS and cRFS. A lymphadenectomy at the time of RP independently improved cRFS (HR 0.09, p = 0.009). The 7-year probability of late Grade 2-3 toxicity was 29% and 5% for genitourinary (GU) and gastrointestinal (GI) symptoms, respectively. The absolute incidence of Grade 3 toxicity was <1% and 10% for GI and GU symptoms, respectively. The study is limited by its retrospective design and the lack of a standardized use of ADT.ConclusionsThis retrospective study shows significantly improved bRFS and cRFS rates with the addition of ADT to HD-ART, with low Grade 3 gastrointestinal toxicity and 10% Grade 3 genitourinary toxicity.Copyright © 2012 Elsevier Inc. All rights reserved.
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