Outcome After Conformal Salvage Radiotherapy in Patients With Rising Prostate-Specific Antigen Levels After Radical Prostatectomy
Creators
- 1. Department of Radiation Oncology, Klinikum rechts der Isar der Technischen Universität München, Munich (Germany)
- 2. Department of Radiation Oncology, Universitätsspital Basel, Basel (Switzerland)
- 3. Department of Oncology and Palliative Medicine, Nordland Hospital, Bodø (Norway)
- 4. Faculty of Health Sciences, University of Tromsø, Tromsø (Norway)
Description
Purpose: This study attempts to improve our understanding of the role of salvage radiotherapy (SRT) in patients with prostate-specific antigen (PSA) relapse after radical prostatectomy with regard to biochemical control, rate of distant metastasis, and survival. Methods and Materials: We performed a retrospective analysis of 96 men treated with conformal prostate bed SRT (median, 64.8 Gy) at a single institution (median follow-up, 70 months). The majority had intermediate- or high-risk prostate cancer. Fifty-four percent underwent a resection with positive margins (R1 resection). The median time interval between surgery and SRT was 22 months. Results: After SRT, 66% of patients reached a PSA nadir of less than 0.2 ng/mL. However, the 5-year biochemical no evidence of disease rate was 35%. Seminal vesicle involvement was predictive for a significantly lower biochemical no evidence of disease rate. All patients with a preoperative PSA level greater than 50 ng/mL relapsed biochemically within 2 years. The 5-year distant metastasis rate was 18%, the 5-year prostate cancer–specific survival rate was 90%, and the 5-year overall survival rate was 88%. Significantly more distant metastases developed in patients with a PSA nadir greater than 0.05 ng/mL after SRT, and they had significantly inferior prostate cancer–specific and overall survival rates. Resection status (R1 vs. R0) was not predictive for any of the endpoints. Conclusions: Men with postoperative PSA relapse can undergo salvage treatment by prostate bed radiotherapy, but durable PSA control is maintained only in about one-third of the patients. Despite a high biochemical failure rate after SRT, prostate cancer–specific survival does not decrease rapidly.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.ijrobp.2011.03.003Additional details
Identifiers
- DOI
- 10.1016/j.ijrobp.2011.03.003;
- PII
- S0360-3016(11)00377-4;
Publishing Information
- Journal Title
- International Journal of Radiation Oncology, Biology and Physics
- Journal Volume
- 82
- Journal Issue
- 5
- Journal Page Range
- p. 1930-1937
- ISSN
- 0360-3016
- CODEN
- IOBPD3
INIS
- Country of Publication
- United States
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 44016635
- Subject category
- S62: RADIOLOGY AND NUCLEAR MEDICINE;
- Descriptors DEI
- ANTIGENS; FAILURES; HAZARDS; MEN; METASTASES; NEOPLASMS; PATIENTS; PROSTATE; RADIOTHERAPY; SURGERY
- Descriptors DEC
- ANIMALS; BODY; DISEASES; GLANDS; MALE GENITALS; MALES; MAMMALS; MAN; MEDICINE; NUCLEAR MEDICINE; ORGANS; PRIMATES; RADIOLOGY; THERAPY; VERTEBRATES
Optional Information
- Copyright
- Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.