Du Chigang, Ren Junquan, Zhang Rui, Xin Tao, Li Zhongmin, Zhang Zhiti, Xu Xinghua, Pang Qi
Department of Neurosurgery, Provincial Hospital Affiliated to Shandong University, Jinan, Shandong, China (mainland).
Department of Blood Transfusion, Liaocheng People's Hospital, Liaocheng, Shandong, China (mainland).
Med Sci Monit. 2016 Sep 29;22:3486-3492. doi: 10.12659/msm.899224.
BACKGROUND MGMT methylation status can influence the therapeutic effect and prognosis of glioblastoma (GBM). There are conflicting results from studies evaluating the efficacy of bevacizumab (BV) when it is combined with temozolomide (TMZ) and radiotherapy (RT) in patients diagnosed with GBM with different MGMT methylation status. MATERIAL AND METHODS Data were extracted from publications in PubMed, Embase, and The Cochrane Library, with the last search performed March 23, 2016. Data on overall survival (OS), progression-free survival (PFS), and MGMT methylation status were obtained. RESULTS Data from 3 clinical trials for a total of 1443 subjects were used for this meta-analysis. MGMT methylated and unmethylated patients showed improved PFS in the BV group (pooled HRs, 0.769, 95% CIs 0.604-0.978, P=0.032; 0.675, 95%CIs 0.466-0.979, P=0.038). For patients with either type of GBM, BV did not improve the OS based on the pooled HRs 1.132 (95% CIs 0.876-1.462; P=0.345) for methylated and 1.018 (95% CIs 0.879-1.179; P=0.345) for unmethylated. CONCLUSIONS Bevacizumab combined with temozolomide-radiotherapy correlated with improved PFS for treatment of patients with different MGMT methylation status of newly diagnosed GBM. There was insufficient evidence to determine the synergistic effects of combining BV with TMZ and RT on improving survival in patients with different MGMT methylation status.
背景 甲基鸟嘌呤-DNA甲基转移酶(MGMT)甲基化状态可影响胶质母细胞瘤(GBM)的治疗效果和预后。在评估贝伐单抗(BV)联合替莫唑胺(TMZ)及放疗(RT)对不同MGMT甲基化状态的GBM患者疗效的研究中,结果存在矛盾。
材料与方法 数据来自于PubMed、Embase和Cochrane图书馆的出版物,最后一次检索于2016年3月23日进行。获取总生存期(OS)、无进展生存期(PFS)及MGMT甲基化状态的数据。
结果 来自3项临床试验共1443名受试者的数据用于该荟萃分析。MGMT甲基化和未甲基化患者在BV组中PFS均有改善(合并风险比,0.769,95%置信区间0.604 - 0.978,P = 0.032;0.675,95%置信区间0.466 - 0.979,P = 0.038)。对于两种类型的GBM患者,基于合并风险比,甲基化患者的OS未改善,为1.132(95%置信区间0.876 - 1.462;P = 0.345),未甲基化患者为1.018(95%置信区间0.879 - 1.179;P = 0.345)。
结论 贝伐单抗联合替莫唑胺 - 放疗与新诊断GBM不同MGMT甲基化状态患者治疗时PFS改善相关。尚无足够证据确定BV联合TMZ及RT对不同MGMT甲基化状态患者改善生存的协同作用。