Modifying radical radiotherapy in high grade gliomas; Shortening the treatment time through acceleration

Citation
M. Brada et al., Modifying radical radiotherapy in high grade gliomas; Shortening the treatment time through acceleration, INT J RAD O, 43(2), 1999, pp. 287-292
Citations number
19
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Onconogenesis & Cancer Research
Journal title
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS
ISSN journal
03603016 → ACNP
Volume
43
Issue
2
Year of publication
1999
Pages
287 - 292
Database
ISI
SICI code
0360-3016(19990115)43:2<287:MRRIHG>2.0.ZU;2-K
Abstract
Purpose: To evaluate the efficacy and toxicity of accelerated radiotherapy in patients with primary high grade glioma, where acceleration is used as a means of delivering a shortened course of radical radiotherapy. Patients and methods: Two-hundred and eleven patients with primary high gra de glioma were treated at the Royal Marsden NHS Trust between 1987 and 1997 with accelerated radiotherapy (55 Gy in 34 fractions twice daily), to plan ning target volume (PTV) defined as enhancing tumour and a 3 cm margin. All had histologically confirmed high grade glioma (53 anaplastic astrocytoma, 137 glioblastoma multiforme, 4 gliosarcoma, 5 gemistocytic astrocytoma, 12 high grade astrocytoma not otherwise specified). The mean Karnofsky perfor mance status (KPS) was 90 and median age was 54 years (range 19-77). Results: Of 211 patients entered, 201 were able to complete radiotherapy; 3 9 patients (19%) had deterioration in KPS during radiotherapy and this was transient in 11. Median survival of 211 patients was 10 months with 1 year, 2 year, and 3 year survival probabilities of 38%, 14%, and 8% respectively . Age and extent of excision were independent prognostic factors for surviv al. Previous comparison to matched cohort receiving 60 Gy in 30 daily fract ions did not demonstrate significant survival difference. Conclusion: Accelerated radiotherapy is a feasible treatment approach for p atients with high grade glioma. The survival and functional outcome are com parable to conventional radiotherapy and the treatment is without serious a cute toxicity. While acceleration of conventional dose irradiation could be tested in randomised studies, it is unlikely this approach would result in a clinically meaningful survival benefit. Accelerated radiotherapy therefo re remains one of the ways of delivering radical irradiation in patients wi th high grade glioma. However, it adds complexity to what is a palliative t reatment regimen and the rationale and advisability should be re-examined, particularly in terms of impact on quality of life, true patient preference , and health economic considerations. (C) 1999 Elsevier Science Inc.