Department of Neurology, University of Virginia, Charlottesville, Virginia.
Department of Neurology, Erasmus MC Cancer Institute, Rotterdam, The Netherlands.
Neuro Oncol. 2019 Jul 11;21(7):837-853. doi: 10.1093/neuonc/noz033.
The finding that most grades II and III gliomas harbor isocitrate dehydrogenase (IDH) mutations conveying a relatively favorable and fairly similar prognosis in both tumor grades highlights that these tumors represent a fundamentally different entity from IDH wild-type gliomas exemplified in most glioblastoma. Herein we review the most recent developments in molecular neuropathology leading to reclassification of these tumors based upon IDH and 1p/19q status, as well as the potential roles of methylation profiling and deletional analysis of cyclin-dependent kinase inhibitor 2A and 2B. We discuss the epidemiology, clinical manifestations, benefit of surgical resection, and neuroimaging features of lower-grade gliomas as they relate to molecular subtype, including advanced imaging techniques such as 2-hydroxyglutarate magnetic resonance spectroscopy and amino acid PET scanning. Recent, ongoing, and planned studies of radiation therapy and both cytotoxic and targeted chemotherapies are summarized, including both small molecule and immunotherapy approaches specifically targeting the mutant IDH protein.
研究发现,大多数 II 级和 III 级神经胶质瘤存在异柠檬酸脱氢酶(IDH)突变,这在两种肿瘤级别中都传递了相对较好且相当相似的预后,这突出表明这些肿瘤与 IDH 野生型神经胶质瘤代表了一种从根本上不同的实体,后者在大多数胶质母细胞瘤中得到了例证。在此,我们回顾了分子神经病理学的最新进展,这些进展导致了基于 IDH 和 1p/19q 状态对这些肿瘤进行重新分类,以及甲基化分析和细胞周期蛋白依赖性激酶抑制剂 2A 和 2B 的缺失分析的潜在作用。我们讨论了与分子亚型相关的低级别神经胶质瘤的流行病学、临床表现、手术切除的益处以及神经影像学特征,包括 2-羟基戊二酸磁共振波谱和氨基酸 PET 扫描等先进的成像技术。总结了放射治疗以及细胞毒性和靶向化疗的最近、正在进行和计划中的研究,包括专门针对突变 IDH 蛋白的小分子和免疫疗法方法。