Ontada, Irving, TX 75039, USA.
Bristol Myers Squibb, Lawrenceville, NJ 08648, USA.
CNS Oncol. 2021 Sep 1;10(3):CNS76. doi: 10.2217/cns-2021-0007. Epub 2021 Aug 11.
Investigate real-world outcomes and healthcare utilization of patients with glioblastoma multiforme (GBM) related to O-methylguanine DNA methyltransferase (MGMT) promoter testing and methylation. US Oncology Network data were analyzed for patients receiving first-line (1L) treatment for GBM. Most patients received 1L radiation with temozolomide. Unadjusted median overall survival (OS) was higher in tested versus untested (median:18.1 vs 11.8 months) and in methylated versus unmethylated (median: 25.5 vs 12.4 months). Untested status, unmethylated MGMT and older age were associated with reduced OS and longer 1L treatment with increased OS. Similar findings were observed for progression-free survival. Utilization was similar between cohorts. In community oncology practices, MGMT methylation and testing were predictive of better survival in GBM.
调查与 O-甲基鸟嘌呤 DNA 甲基转移酶(MGMT)启动子检测和甲基化相关的多形性胶质母细胞瘤(GBM)患者的真实世界结局和医疗保健利用情况。对接受一线(1L)GBM 治疗的患者的美国肿瘤学网络数据进行了分析。大多数患者接受了替莫唑胺联合放疗。未经调整的中位总生存期(OS)在经过检测的患者中高于未经检测的患者(中位:18.1 个月 vs 11.8 个月),在甲基化患者中高于非甲基化患者(中位:25.5 个月 vs 12.4 个月)。未经检测、非甲基化 MGMT 和年龄较大与 OS 降低以及 1L 治疗时间延长相关,而 OS 延长。无进展生存期也观察到类似的结果。两个队列的利用率相似。在社区肿瘤学实践中,MGMT 甲基化和检测可预测 GBM 的生存改善。