Hypofractionated radiotherapy for poor prognosis malignant glioma: matched pair survival analysis with MRC controls

被引:46
作者
McAleese, JJ
Stenning, SP
Ashley, S
Traish, D
Hines, F
Sardell, S
Guerrero, D
Brada, M
机构
[1] Inst Canc Res, Neurooncol Unit, Sutton SM2 5PT, Surrey, England
[2] Royal Marsden NHS Trust, Sutton SM2 5PT, Surrey, England
[3] Inst Canc Res, Acad Unit Radiotherapy & Oncol, Sutton SM2 5PT, Surrey, England
[4] MRC, Clin Trials Unit, London, England
基金
英国医学研究理事会;
关键词
radiotherapy; high grade glioma; palliation;
D O I
10.1016/S0167-8140(03)00077-X
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To assess the survival benefit of palliative hypofractionated radiotherapy in patients with poor prognosis high grade glioma by a matched comparison to conventionally treated controls. Method: Ninety-two elderly and/or disabled patients with high grade glioma with poor prognostic features received palliative partial brain radiotherapy to a dose of 30 Gy in six fractions over 2 weeks. Patients were matched for WHO histological grade, performance status and age from a cohort of patients treated with conventionally fractionated radiotherapy to a dose of 60 Gy in 30 fractions in an Medical Research Council (MRC) BR05 trial. Results: Patients treated with hypofractionated radiotherapy had a median survival of 5 months with a 1-year survival rate of 12% from diagnosis. The median survival of case-matched controls was estimated to be 2.5-4.5 months longer. Following hypofractionated radiotherapy, Barthel score was improved or remained stable in 68% of patients. Conclusion: Hypofractionated partial brain radiotherapy is a well-tolerated regimen with palliative benefit. Comparison with matched controls suggests lesser survival benefit than would be obtained with radical radiotherapy. However, this is compensated by lower intensity and duration of irradiation induced side effects. It is postulated that there may not be a significant difference in good quality survival or,quality adjusted survival' between the two regimens and this requires testing in prospective trials. (C) 2003 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:177 / 182
页数:6
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