Zhao Hailong, Wang Shuying, Song Chengwei, Zha Yunhong, Li Li
Department of Neurology, The First Hospital of Yichang, Institute of Translational Neuroscience, Three Gorges University College of Medicine, Yichang, People's Republic of China.
Wuhan Institute of Biological Products Co., Ltd., Wuhan, People's Republic of China.
World J Surg Oncol. 2016 Oct 12;14(1):261. doi: 10.1186/s12957-016-1012-4.
The prognostic value of the status of O-methylguanine-DNA methyltransferase (MGMT) promoter methylation measured by pyrosequencing assay (PSQ) among glioblastoma (GBM) patients was examined in meta-analysis.
Eligible studies that reported the association between the status of MGMT promoter methylation by PSQ and prognostic value of GBM patients from three electronic databases, like PubMed, EMBASE, and Cochrane library were involved in meta-analysis. Using Stata 11.0, the summarized hazard ratios (HRs) for overall survival (OS) and the progression-free survival (PFS) with 95 % confidence interval (CI) were calculated.
Eleven studies were included to evaluate the relationship between the status of MGMT promoter methylation and GBM patients' survival. Overall, regardless of the cut-off value of methylation status of MGMT promoter by PSQ, methylated-positive patients were evidently associated with an improved HRs for OS (HRs = 0.50, 95 % CI = 0.35-0.66). For summary, progression-free survival (PFS) from four studies, the prognostic effect was also found (HRs = 0.56, 95 % CI = 0.32-0.80).
Methylation positivity of MGMT promoter by PSQ was related to an increased survival in GBM patients. Thus, the status of MGMT promoter methylation by PSQ might be used to be a prognostic biomarker, and GBM patients might have a vested interest in clinical application of standardized PSQ.
通过焦磷酸测序法(PSQ)检测的O-甲基鸟嘌呤-DNA甲基转移酶(MGMT)启动子甲基化状态在胶质母细胞瘤(GBM)患者中的预后价值在荟萃分析中进行了研究。
纳入来自三个电子数据库(如PubMed、EMBASE和Cochrane图书馆)的符合条件的研究,这些研究报告了通过PSQ检测的MGMT启动子甲基化状态与GBM患者预后价值之间的关联。使用Stata 11.0计算总生存期(OS)和无进展生存期(PFS)的汇总风险比(HRs)及95%置信区间(CI)。
纳入11项研究以评估MGMT启动子甲基化状态与GBM患者生存之间的关系。总体而言,无论PSQ检测的MGMT启动子甲基化状态的截断值如何,甲基化阳性患者的OS的HRs明显改善(HRs = 0.50,95% CI = 0.35 - 0.66)。总之,在四项研究的无进展生存期(PFS)中也发现了预后效应(HRs = 0.56,95% CI = 0.32 - 0.80)。
通过PSQ检测的MGMT启动子甲基化阳性与GBM患者生存率增加有关。因此,通过PSQ检测的MGMT启动子甲基化状态可能用作预后生物标志物,并且GBM患者可能会从标准化PSQ的临床应用中受益。