Prognostic and therapeutic factors of gliosarcoma from a multi-institutional series

被引:0
|
作者
J. Castelli
L. Feuvret
Q. C. Haoming
J. Biau
E. Jouglar
A. Berger
G. Truc
F. Llamas Gutierrez
X. Morandi
P. J. Le Reste
F. Thillays
D. Loussouarn
E. Nouhaud
G. Crehange
D. Antoni
E. Vauleon
R. de Crevoisier
G. Noel
机构
[1] Centre Eugene Marquis,Department of Radiotherapy
[2] La Pitié – Salpétrière,Department of Radiotherapy
[3] University of Rochester Medical Center,Radiation Oncology Department
[4] Centre Jean Perrin,Radiotherapy Department
[5] Institut de cancérologie de l’Ouest,Radiotherapy Department
[6] CHU de Poitiers,Department of Radiotherapy
[7] Centre Georges François Leclerc,Radiotherapy Department
[8] CHU de Rennes,Department of Pathology
[9] CHU de Rennes,Department of Neurosurgery
[10] CHU de Nantes,Department of Pathology
[11] Centre Eugene Marquis,Department of Oncology
[12] Centre Paul Strauss,Department of Radiotherapy
来源
Journal of Neuro-Oncology | 2016年 / 129卷
关键词
Gliosarcoma; Radiotherapy; Temozolomide;
D O I
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中图分类号
学科分类号
摘要
The aims of this multicentre retrospective study were to identify prognostic or therapeutic factors impacting on overall survival in patients with gliosarcoma. The analysis included all patients treated for gliosarcoma between 1998 and 2014 in seven French academic centres. Seventy-five patients with a median age of 60 years (range from 23 to 79 years) were treated with a combination of surgery (n = 66), radiotherapy (adjuvant for 64 patients and exclusive for 8 patients) and temozolomide based chemotherapy (n = 58). Median follow-up was 12 months (range from 2 to 71 months). Two-year overall survival (OS) and disease free survival rates were 12 % (95 % CI 4–20 %) and 2 % (95 % CI 0–6 %), respectively. The median OS was 13 months. Treatment at recurrence consisted of chemotherapy (n = 38) (bevazicumab for 18 patients, repeat temozolomide for 10 patients), salvage surgery (n = 8) and radiochemotherapy (n = 1). In univariate analysis, younger age, higher total dose of radiotherapy, longer time to recurrence and treatment at recurrence significantly increased OS. In multivariate analysis, high total dose of radiotherapy (HR = 0.97, p = 0.007) and treatment at recurrence (HR = 0.28, p < 0.001) were favourable prognostic factors of OS. Radiotherapy at a minimum dose of 54 Gy and salvage treatment increased OS of gliosarcoma. Unlike glioblastoma, in our analysis, TMZ based chemotherapy was not associated with an improvement in OS compared to patients who received radiation therapy only.
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页码:85 / 92
页数:7
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