Omuro Antonio M, Delattre Jean-Yves
Curr Opin Neurol. 2007 Dec;20(6):704-7. doi: 10.1097/WCO.0b013e3282f1beef.
In this editorial, we seek to critically analyse currently available options for the treatment of gliomas in order to provide guidance for evidence-based therapeutic decisions.
Several recently reported trials in gliomas have investigated ways of optimizing traditional treatments (i.e. radiotherapy and cytotoxic chemotherapy), as well as novel approaches such as molecularly targeted therapy.
Chemotherapy with temozolomide concomitant with radiotherapy remains a standard of care for glioblastoma, but current efforts are concentrated on confirming phase II results of protracted temozolomide schedules. The role of chemotherapy for grade III and II gliomas lacks phase III evidence but several trials are ongoing. Such trials are stratified by (or designed separately according to) chromosomes 1p/19q codeletion status, and such genetic analysis will thus be essential for therapeutic decisions in the future. The single positive results with targeted therapy remain to date the high response rates with bevacizumab and irinotecan in a phase II trial for recurrent malignant gliomas. Several questions regarding survival benefits and toxicity remain, however. Results of randomized trials of bevacizumab-based combinations are eagerly awaited, and if positive, they will point to antiangiogenesis strategies as the most promising current investigation venue in gliomas.
在这篇社论中,我们旨在批判性地分析目前可用于治疗胶质瘤的方法,以便为基于证据的治疗决策提供指导。
最近在胶质瘤中报道的几项试验研究了优化传统治疗方法(即放疗和细胞毒性化疗)的方式,以及诸如分子靶向治疗等新方法。
替莫唑胺同步放疗仍是胶质母细胞瘤的标准治疗方案,但目前的工作集中在确认延长替莫唑胺给药方案的II期试验结果。化疗对III级和II级胶质瘤的作用缺乏III期证据,但多项试验正在进行。此类试验根据1p/19q染色体缺失状态进行分层(或单独设计),因此这种基因分析对未来的治疗决策至关重要。靶向治疗的唯一阳性结果是贝伐单抗和伊立替康在复发性恶性胶质瘤II期试验中的高缓解率。然而,关于生存获益和毒性仍有几个问题。基于贝伐单抗联合治疗的随机试验结果备受期待,如果结果为阳性,将表明抗血管生成策略是目前胶质瘤研究中最有前景的方向。