Radiochemotherapy in patients with primary glioblastoma comparing two temozolomide dose regimens

被引:35
作者
Combs, Stephanie E. [1 ]
Wagner, Johanna
Bischof, Marc
Welzel, Thomas
Edler, Lutz [2 ]
Rausch, Renate [2 ]
Wagner, Florian
Bois, Angelika Zabel-Du
Debus, Juergen
Schulz-Ertner, Daniela
机构
[1] Univ Heidelberg, Neuroradiat Oncol Res Grp, Dept Radiat Oncol, D-69120 Heidelberg, Germany
[2] German Canc Res Ctr, Dept Biostat, D-6900 Heidelberg, Germany
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2008年 / 71卷 / 04期
关键词
glioblastoma; radiochemotherapy; temozolomide; outcome; toxicity;
D O I
10.1016/j.ijrobp.2007.11.064
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To evaluate toxicity and outcomes in patients with primary glioblastoma (GB) treated with postoperative radiochemotherapy (RCHT) with temozolomide (TMZ) comparing two dose regimens. Methods and Materials: A total of 160 patients with histologically confirmed GB were treated with postoperative RCHT with TMZ. Of the patients, 66 were female and 94 were male, with a median age of 60 years. After the primary diagnosis, a biopsy had been performed in 42 patients; a subtotal and total resection was conducted in 66 and 52 patients. Postoperative radiotherapy was applied with a median dose of 60 Gy with a median fractionation of 5 x 2Gy/week. Concomitant TMZ was prescribed at 50 mg/m(2) in 123 patients (Group A) and at 75 mg/m(2) in 37 patients (Group B). Patients were followed in 3-months intervals, with a median follow-up of 13 months. Results: Overall survival (OS) rates in Group A vs. Group B were 67% and 79% at 1 year and 43% vs. 49% at 2 years, respectively (p = 0.69). Progression-free survival was 49% vs. 54% at 1 year and 22% vs. 29% at 2 years (p = 0.31). Hematologic toxicity was not statistically significant over the 6-week RCHT period except for a significant decrease in platelets during Week 6 (p = 0.01) in Group B. Conclusions: Overall survival seems to be comparable in both groups, although longer follow-up and a larger group of patients are needed to corroborate these results. Lower dosing of TMZ also is associated with a more beneficial toxicity profile. (C) 2008 Elsevier Inc.
引用
收藏
页码:999 / 1005
页数:7
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