Image-guided dose-escalated intensity-modulated radiation therapy for prostate cancer: treating to doses beyond 78 Gy

被引:28
|
作者
Eade, Thomas N. [1 ]
Guo, Linxin [1 ]
Forde, Elizabeth [1 ]
Vaux, Ken [2 ]
Vass, Justin [2 ]
Hunt, Peter [1 ]
Kneebone, Andrew [1 ]
机构
[1] Royal N Shore Hosp, Dept Radiat Oncol, Sydney, NSW 2065, Australia
[2] Royal N Shore Hosp, Dept Urol, Sydney, NSW 2065, Australia
关键词
prostate cancer; radiotherapy; IMRT; dose escalation; EXTERNAL-BEAM RADIOTHERAPY; CONFORMAL RADIOTHERAPY; ACUTE TOXICITY; LOW-RISK; TRIAL; DOSIMETRY;
D O I
10.1111/j.1464-410X.2011.10668.x
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Study Type Therapy (case series) Level of Evidence 4 What's known on the subject? and What does the study add? High doses of radiotherapy correspond to higher cure rates. Most radiation centers in the UK and Australia limit prescription doses to 7478 Gy and do not use IGRT and IMRT for all patients. The combination of IGRT and IMRT can limit the rectum and bladder to low doses allowing doses above 78 Gy to be delivered, including pelvic lymph node treatment, with low side effects. This paper provides a detailed guide of planning technique and expected toxicity to enable implementation of similar dose escalated prostate programmes in other radiotherapy centres. OBJECTIVE To determine the short-term side-effects of dose-escalated image-guided intensity-modulated radiation therapy (IG-IMRT) for the definitive treatment of prostate cancer. PATIENTS AND METHODS Eligible patients were treated at doses >78 Gy and with definitive intent. Patients from a prospective database with International Prostate Symptom Score (IPSS) and Common Terminology Criteria for Adverse Events, version 3.0 (CTCAE) toxicity were recorded weekly during treatment and at follow-up. RESULTS In all, 101 patients were included, with doses ranging from 78.3 to 84 Gy (median = 79.3). The median (range) age was 71 (4683) years; 60% received concurrent androgen deprivation and 35% had pelvic lymph node treatment. The median (range) IPSS at baseline, on treatment and at first follow-up were 7 (035), 15 (134) and 6 (030), respectively. The percentages of patients with grade 2 or higher toxicity during treatment, at 3 months and at 2 years were, respectively, 6.9%, 1% and 2% for gastrointestinal symptoms and 39%, 6.9% and 3% for genitourinary symptoms. There was no significant difference in gastrointestinal toxicity during treatment (P= 0.860) or at 3 months (P= 0.334) between patients with and without lymph node treatment. CONCLUSION Doses >78 Gy delivered using daily image guidance and IMRT are well tolerated, and by 3 months short-term side-effects have normalized for the majority of patients.
引用
收藏
页码:1655 / 1660
页数:6
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