Two decades of high dose rate brachytherapy with external beam radiotherapy for prostate cancer

被引:19
|
作者
Astrom, Lennart [1 ]
Grusell, Erik [2 ]
Sandin, Fredrik [3 ]
Turesson, Ingela [1 ]
Holmberg, Lars [4 ,5 ]
机构
[1] Uppsala Univ, Sect Clin & Expt Oncol, Dept Immunol Genet & Pathol IGP, Uppsala, Sweden
[2] Uppsala Univ, Sect Med Radiat Sci, IGP, Uppsala, Sweden
[3] Reg Canc Ctr Uppsala Orebro, Uppsala, Sweden
[4] Uppsala Univ, Dept Surg Sci, Uppsala, Sweden
[5] Kings Coll London, Fac Life Sci & Med, London, England
关键词
Prostate cancer; Radiotherapy; Brachytherapy; High dose rate; ANDROGEN SUPPRESSION; RADIATION-THERAPY; RANDOMIZED-TRIAL; BONE METASTASES; RISK-FACTORS; SHORT-TERM; ESCALATION; BOOST; IRRADIATION; FAILURE;
D O I
10.1016/j.radonc.2017.12.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: High-dose-rate brachytherapy (HDR-BT) has optimal prerequisites in radiotherapy of prostate cancer (PC) with a conformal dose distribution and high doses per fraction giving a biological dose escalation. We report the outcome after HDR-BT and external beam radiotherapy (EBRT) after 20 years of experience. Material and methods: The study includes 623 patients, median age of 66 years, treated from 1995 to 2008 and a median follow up of 11 years (range 2-266 months). Androgen deprivation therapy was given to 429 patients (69%). The HDR-BT was given with two 10 Gy fractions and the EBRT with 2 Gy fractions to 50 Gy. Results: The 10-year PC-specific survival was 100%, 92%, 91%, and 75% for low-, intermediate-, high-and very high-risk patients respectively, and the 10-year probability of PSA relapse was 0%, 21%, 33%, and 65% respectively. The 10-year actuarial prevalence for >= grade 2 GU-and GI-toxicities were 28% and 12% respectively and for >= grade 3, 4% and 1% respectively. Urethral stricture was the most frequent GU complication with a 10-year actuarial incidence of 10%. Treatment without dose constraints for the urethra conferred a higher incidence 18%, compared to 5% after 2003 (p < 0.001). Sixteen patients experienced grade 4 GU toxicity, of which 13 were treated before 2003. No grade 4 rectal toxicity was seen. Conclusion: The combination of EBRT and HDR-BT with adequate dose constraints to risk organs provides satisfactory long-term tumour control even in high-risk patients. GI toxicity stabilised but GU toxicity progressed during the 10-year follow up. (C) 2018 Elsevier B. V. All rights reserved.
引用
收藏
页码:81 / 87
页数:7
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