Phase II trial of radiation dose escalation with conformal external beam radiotherapy and high-dose-rate brachytherapy combined with long-term androgen suppression in unfavorable prostate cancer: feasibility report

Autor: Pilar Romero, Mauricio Cambeiro, Raquel Ciérvide, Mercedes Teijeira, Carlos Galán, M. Moreno, José Javier Aristu, Jeanette Valero, Javier Zudaire, Rafael Martínez-Monge
Rok vydání: 2008
Předmět:
Zdroj: International journal of radiation oncology, biology, physics. 76(2)
ISSN: 1879-355X
Popis: Purpose To determine the feasibility of combined long-term luteinizing hormone-releasing hormone agonist–based androgen suppressive therapy (AST) and dose escalation with high-dose-rate (HDR) brachytherapy for high-risk (HRPC) or very-high-risk prostate cancer (VHRPC). Methods and Materials Between January 2001 and October 2006, 134 patients (median age, 70 years) with either National Comprehensive Cancer Network criteria–defined HRPC ( n = 47, 35.1%) or VHRPC ( n = 87, 64.9%) were prospectively enrolled in this Phase II trial. Tumor characteristics included a median pretreatment prostate-specific antigen level of 14.6 ng/mL, a median clinical stage of T2c, and a median Gleason score of 7. Three-dimensional conformal radiotherapy (54 Gy in 30 fractions) was followed by HDR brachytherapy (19 Gy in 4 b.i.d. treatments). Androgen suppressive therapy started 0–3 months before three-dimensional conformal radiotherapy and continued for 2 years. Results One implant was repositioned with a new procedure (0.7%). Five patients (3.7%) discontinued AST at a median of 13 months (range, 6–18 months) because of disease progression ( n = 1), hot flashes ( n = 2), fatigue ( n = 1), and impotence ( n = 1). After a median follow-up of 37.4 months (range, 24–90 months), the highest Radiation Therapy Oncology Group–defined late urinary toxicities were Grade 0 in 47.8%, Grade 1 in 38.1%, Grade 2 in 7.5%, and Grade 3 in 6.7% of patients. Maximal late gastrointestinal toxicities were Grade 0 in 73.1%, Grade 1 in 16.4%, Grade 2 in 7.5%, and Grade 3 in 2.9% of patients. There were no Grade 4 or 5 events. Conclusions Intermediate-term results show that dose escalation with HDR brachytherapy combined with long-term AST is feasible and has a toxicity profile similar to that reported by previous HDR brachytherapy studies.
Databáze: OpenAIRE