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替莫唑胺联合加速放疗治疗多形性胶质母细胞瘤可延长生存期。

Prolonged survival when temozolomide is added to accelerated radiotherapy for glioblastoma multiforme.

机构信息

Department of Radiation Oncology, University Hospital Würzburg, Würzburg, Germany.

出版信息

Strahlenther Onkol. 2011 Sep;187(9):548-54. doi: 10.1007/s00066-011-2242-6. Epub 2011 Aug 18.

Abstract

BACKGROUND

The goal of this study was to evaluate accelerated radiotherapy with and without temozolomide (TMZ) for glioblastoma multiforme (GBM).

METHODS

This retrospective analysis evaluated 86 patients with histologically proven GBM who were treated with accelerated radiotherapy of 1.8 Gy twice daily to a total dose of 54 Gy within 3 weeks. Median age was 62 years and median Karnofsky index was 90. A total of 41 patients received radiotherapy only from 2002-2005 and 45 patients were treated with TMZ concomitantly and after radiotherapy from 2005-2007.

RESULTS

Median overall survival (OS) was 12.5 months and 2-year OS was 15.4%. Patient characteristics were well balanced between the two groups except for better performance status (p = 0.05) and higher frequency of retreatment for the first recurrence (p = 0.02) in the TMZ group. Age at diagnosis (HR 2.83) and treatment with TMZ (HR 0.60) were correlated with OS in the multivariate analysis: treatment with and without TMZ resulted in median OS of 16 months and 11.3 months, respectively. Hematological toxicity grade > II was observed in 2/45 patients and 5/37 patients during simultaneous radiochemotherapy and adjuvant TMZ.

CONCLUSION

TMZ added to accelerated radiotherapy for GBM resulted in prolonged overall survival with low rates of severe hematological toxicity.

摘要

背景

本研究旨在评估替莫唑胺(TMZ)联合或不联合加速放疗治疗多形性胶质母细胞瘤(GBM)的效果。

方法

本回顾性分析纳入了 86 例经组织学证实的 GBM 患者,他们接受了 1.8 Gy 的加速放疗,每天两次,总剂量为 54 Gy,3 周内完成。中位年龄为 62 岁,中位卡氏功能状态评分(KPS)为 90。2002 年至 2005 年期间,41 例患者仅接受放疗,2005 年至 2007 年期间,45 例患者接受 TMZ 同步放化疗和放疗后治疗。

结果

中位总生存期(OS)为 12.5 个月,2 年 OS 为 15.4%。两组患者的特征基本平衡,除了 TMZ 组的功能状态较好(p = 0.05)和首次复发后的再治疗频率较高(p = 0.02)。多因素分析显示,诊断时年龄(HR 2.83)和 TMZ 治疗(HR 0.60)与 OS 相关:TMZ 联合和不联合加速放疗的中位 OS 分别为 16 个月和 11.3 个月。在同步放化疗和辅助 TMZ 治疗期间,有 2/45 例和 5/37 例患者出现血液学毒性> II 级。

结论

TMZ 联合加速放疗治疗 GBM 可延长总体生存时间,且严重血液学毒性发生率较低。

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