| Literature DB >> 30753579 |
David Schiff1, Martin Van den Bent2, Michael A Vogelbaum3, Wolfgang Wick4, C Ryan Miller5, Martin Taphoorn6, Whitney Pope7, Paul D Brown8, Michael Platten9, Rakesh Jalali10, Terri Armstrong11, Patrick Y Wen12.
Abstract
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.Entities:
Keywords: IDH mutation; astrocytoma; glioma; lower-grade; oligodendroglioma
Year: 2019 PMID: 30753579 PMCID: PMC6620638 DOI: 10.1093/neuonc/noz033
Source DB: PubMed Journal: Neuro Oncol ISSN: 1522-8517 Impact factor: 12.300