Published November 27, 2013 | Version v1
Journal article

Dose-escalated salvage radiotherapy after radical prostatectomy in high risk prostate cancer patients without hormone therapy: outcome, prognostic factors and late toxicity

  • 1. Department of Radiation Oncology, University Medical Center Mannheim, University of Heidelberg, Mannheim (Germany)
  • 2. Department of Radiation Oncology and Nuclear Medicine (NEMROCK), Faculty of Medicine, Cairo University, Cairo (Egypt)
  • 3. Department of Urology, University Medical Center Mannheim, University of Heidelberg, Mannheim (Germany)

Description

Evaluation of dose escalated salvage radiotherapy (SRT) in patients after radical prostatectomy (RP) who had never received antihormonal therapy. To investigate prognostic factors of the outcome of SRT and to analyze which patient subsets benefit most from dose escalation. Between 2002 and 2008, 76 patients were treated in three different dose-groups: an earlier cohort treated with 66 Gy irrespective of pre-RT-characteristics and two later cohorts treated with 70 Gy or 75 Gy depending on pre-RT-characteristics. Biochemical-relapse-free-survival (bRFS), clinical-relapse-free-survival (cRFS) and late toxicity were evaluated. Four-year bRFS and cRFS were 62.5% and 85%. Gleason score <8, positive surgical resection margin (PSRM) and low PSA (≤0.5 ng/ml) before SRT resulted in higher bRFS. Analysis of the whole group showed no clear dose-outcome relationship. Patients with PSRM, however, had improved bRFS when escalating >66 Gy. While > 70 Gy did not improve the overall results, 4-year bRFS for patients with manifest local recurrence in the high-dose group was still comparable to those without manifest local recurrences. No grade 4 and minimal grade 3 gastrointestinal and urinary toxicity were observed. Dose-escalated SRT achieves high biochemical control. The data strongly support the application of at least 70 Gy rather than 66 Gy. They do not prove positive effects of doses >70 Gy but do not disprove them as these doses were only applied to an unfavorable patients selection

Availability note (English)

Available from http://dx.doi.org/10.1186/1748-717X-8-276; Available from http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4222032

Additional details

Publishing Information

Journal Title
Radiation Oncology (Online)
Journal Volume
8
Journal Page Range
p. 276
ISSN
1748-717X

INIS

Country of Publication
United Kingdom
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
47066145
Subject category
S62: RADIOLOGY AND NUCLEAR MEDICINE;
Descriptors DEI
GY RANGE 10-100; PATIENTS; RADIATION DOSES; RADICALS; RADIOTHERAPY; TOXICITY
Descriptors DEC
ABSORBED DOSE RANGE; DOSES; GY RANGE; MEDICINE; NUCLEAR MEDICINE; RADIATION DOSE RANGES; RADIOLOGY; THERAPY

Optional Information

Copyright
Copyright (c) 2013 Shelan et al.
Notes
PMCID: PMC4222032; PUBLISHER-ID: 1748-717X-8-276; PMID: 24279376; OAI: oai:pubmedcentral.nih.gov:4222032; licensee BioMed Central Ltd.