Corresponding Author: Wolfgang Wick, MD, Department of Neurooncology, National Center for Tumor Diseases and Neurology Clinic, University Clinic Heidelberg and German Cancer Research Centre, Im Neuenheimer Feld 400, 69120-Heidelberg, Germany.
Neuro Oncol. 2013 Oct;15(10):1405-12. doi: 10.1093/neuonc/not100. Epub 2013 Aug 1.
This study's primary objective was evaluation of the progression-free survival rate at 6 months (PFS-6) in patients with newly diagnosed glioblastoma without O(6)-methylguanine-DNA-methyltransferase (MGMT) promoter hypermethylation postsurgically treated with enzastaurin before and concomitantly with radiation therapy, followed by enzastaurin maintenance therapy. PFS-6 of at least 55% was set to be relevant compared with the data of the EORTC 26981/22981 NCIC CE.3 trial.
Adult patients with a life expectancy of at least 12 weeks who were newly diagnosed with a histologically proven supratentorial glioblastoma without MGMT promoter hypermethylation were eligible. Patients were treated with enzastaurin prior to, concomitantly with, and after standard partial brain radiotherapy. Here we report on a multicenter, open-label, uncontrolled phase II study of patients with newly diagnosed glioblastoma without MGMT promoter hypermethylation treated with enzastaurin and radiation therapy within 4 study periods.
PFS-6 was 53.6% (95% confidence interval [CI]: 39.8-65.6). The median overall survival was 15.0 months (95% CI: 11.9-17.9) for all patients, 3.9 months (95% CI: 0.8-9.0) for patients with biopsy, 15.4 months (95% CI: 10.1-17.9) for patients with partial resection, and 18.9 months (95% CI: 13.9-28.5) for patients with complete resection. The safety profile in this study was as expected from previous trials, and the therapy was well tolerated.
PFS-6 missed the primary planned outcome of 55%. The secondary exploratory analysis according to resection status of the different subgroups of patients with biopsies, partial resection, and complete resection demonstrates the strong prognostic influence of resection on overall survival.
本研究的主要目的是评估新诊断的胶质母细胞瘤患者在术后未进行 O(6)-甲基鸟嘌呤-DNA-甲基转移酶(MGMT)启动子超甲基化、接受恩扎司琼术前、同步和放疗后进行治疗的无进展生存期(PFS-6),然后进行恩扎司琼维持治疗。与 EORTC 26981/22981 NCIC CE.3 试验的数据相比,PFS-6 至少为 55%被认为是相关的。
符合条件的患者为预期寿命至少 12 周的新诊断为组织学证实的幕上胶质母细胞瘤且无 MGMT 启动子超甲基化的成年患者。患者在标准部分脑放疗前、同步和之后接受恩扎司琼治疗。在此,我们报告了一项多中心、开放性、非对照的 II 期研究,研究对象为在 4 个研究期内接受恩扎司琼和放疗治疗的无 MGMT 启动子超甲基化新诊断的胶质母细胞瘤患者。
PFS-6 为 53.6%(95%置信区间 [CI]:39.8-65.6)。所有患者的中位总生存期为 15.0 个月(95%CI:11.9-17.9),活检患者为 3.9 个月(95%CI:0.8-9.0),部分切除患者为 15.4 个月(95%CI:10.1-17.9),完全切除患者为 18.9 个月(95%CI:13.9-28.5)。该研究的安全性特征与之前的试验预期一致,且治疗耐受性良好。
PFS-6 未达到 55%的主要计划结局。根据活检、部分切除和完全切除患者的不同亚组的切除状态进行的二次探索性分析表明,切除对总生存期有强烈的预后影响。