High dose brachytherapy (real time) in patients with intermediate-or high-risk prostate cancer: technical description and preliminary experience
Autor: | J. M. Garcia, José Manuel González Sancho, Ángeles de la Rua Calderón, Germán Juan Rijo, Ramón Abascal García, Pedro Gómez, Inmaculada Romo Fonseca, Reinerio Rodríguez-Fernández, José Fernández García, M. Suárez |
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Rok vydání: | 2005 |
Předmět: |
Male
Cancer Research Antineoplastic Agents Hormonal medicine.medical_treatment Brachytherapy Disease-Free Survival law.invention Prostate cancer Postoperative Complications Randomized controlled trial law Prostate medicine Humans Stage (cooking) business.industry Prostatic Neoplasms Cancer Radiotherapy Dosage General Medicine medicine.disease Radiation therapy Treatment Outcome medicine.anatomical_structure Oncology Prostate surgery Nuclear medicine business Follow-Up Studies |
Zdroj: | Clinical and Translational Oncology. 7:389-397 |
ISSN: | 1699-3055 1699-048X |
DOI: | 10.1007/bf02716584 |
Popis: | It has been well documented that the outcome of prostate cancer treatment depends on the dose administered. Hence, techniques have been developed that allow high-dose administration without increasing the complications, e.g. external radiotherapy combined with high-dose radiation (HDR) brachytherapy. In this article we analyse the technique and protocol of real-time HDR brachytherapy together with the preliminary results that support its use. Materials and methods. Between June 1998 and December 2004, 100 patients with adenoma of the prostate were treated with 46 Gy of external irradiation to the pelvis and 2 HDR brachytherapy fractions (each of 1150 cGy) at the end of weeks 1 and 3 of a 5-week radiotherapy course. The 1997 American Joint Commission on Cancer (AJCC) system was used to establish disease stage. Patients with intermediate-risk (PSA 10-20 ng/ml or Gleason = 7 or T2c) and high-risk (two intermediate risk factors or PSA20 ng/ml or Gleason7 orT2c) without metastases were eligible for the brachytherapy. Biochemical failure was defined according to the American Society for Therapeutic Radiology and Oncology (ASTRO) consensus panel statement. SPSS statistical package was used to quantify survival (Kaplan-Meier method). Toxicity was scored according to RTOG guidelines.The mean age of patients was 67 years (range 49-78). Clinical stage was T2a in 22% of the patients, 26% T2b and 52% T3. Initial PSA was = 10 ng/ml in 22% of the patients and10 ng/ml in 78%. Median follow-up was 28 months (range: 12-79). The 5-year overall survival and actuarial biochemical control were 99% and 87% respectively. No chronic severe complications were noted.The good results of local control, disease-free survival and few complications that the external radiotherapy combined with HDR brachytherapy have shown suggest that the method should be considered as first-choice in the treatment of prostate tumours of high- and intermediate-risk. |
Databáze: | OpenAIRE |
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