Division of Neurosurgery, Omi Medical Center, Yabase-cho 1660, Kusatsu, Shiga, 525-8585, Japan.
Department of Neurosurgery, Shiga University of Medical Science, Ohtsu, Japan.
Brain Tumor Pathol. 2023 Jul;40(3):143-157. doi: 10.1007/s10014-023-00463-8. Epub 2023 May 22.
The WHO 2021 classification defines IDH wild type (IDHw) histologically lower-grade glioma (hLGG) as molecular glioblastoma (mGBM) if TERT promoter mutation (pTERTm), EGFR amplification or chromosome seven gain and ten loss aberrations are indicated. We systematically reviewed articles of IDHw hLGGs studies (49 studies, N = 3748) and meta-analyzed mGBM prevalence and overall survival (OS) according to the PRISMA statement. mGBM rates in IDHw hLGG were significantly lower in Asian regions (43.7%, 95% confidence interval [CI: 35.8-52.0]) when compared to non-Asian regions (65.0%, [CI: 52.9-75.4]) (P = 0.005) and were significantly lower in fresh-frozen specimen when compared to formalin-fixed paraffin-embedded samples (P = 0.015). IDHw hLGGs without pTERTm rarely expressed other molecular markers in Asian studies when compared to non-Asian studies. Patients with mGBM had significantly longer OS times when compared to histological GBM (hGBM) (pooled hazard ratio (pHR) 0.824, [CI: 0.694-0.98], P = 0.03)). In patients with mGBM, histological grade was a significant prognostic factor (pHR 1.633, [CI: 1.09-2.447], P = 0.018), as was age (P = 0.001) and surgical extent (P = 0.018). Although bias risk across studies was moderate, mGBM with grade II histology showed better OS rates when compared to hGBM.
世界卫生组织 (WHO) 2021 年的分类将 IDH 野生型(IDHw)组织学低级别胶质瘤(hLGG)定义为分子胶质母细胞瘤(mGBM),如果存在 TERT 启动子突变(pTERTm)、EGFR 扩增或 7 号染色体增益和 10 号染色体缺失异常。我们系统地回顾了 IDHw hLGG 研究的文章(49 项研究,N=3748),并根据 PRISMA 声明对 mGBM 的患病率和总生存期(OS)进行了荟萃分析。与非亚洲地区(65.0% [95%置信区间(CI):52.9-75.4])相比,亚洲地区 IDHw hLGG 中的 mGBM 发生率明显较低(43.7%,[CI:35.8-52.0])(P=0.005),且在新鲜冷冻标本中与福尔马林固定石蜡包埋样本相比明显较低(P=0.015)。与非亚洲研究相比,在亚洲研究中,没有 pTERTm 的 IDHw hLGG 很少表达其他分子标志物。与组织学胶质母细胞瘤(hGBM)相比,mGBM 患者的 OS 时间明显更长(合并危险比(pHR)0.824,[CI:0.694-0.98],P=0.03))。在 mGBM 患者中,组织学分级是一个显著的预后因素(pHR 1.633,[CI:1.09-2.447],P=0.018),年龄(P=0.001)和手术范围(P=0.018)也是显著的预后因素。尽管研究之间的偏倚风险为中度,但具有 II 级组织学特征的 mGBM 与 hGBM 相比,OS 率更好。