| Literature DB >> 31989507 |
Christina Coleman1, Schuyler Stoller2, Michael Grotzer3, Ana Guerreiro Stucklin3, Javad Nazarian3, Sabine Mueller4,5,6,7.
Abstract
Pediatric high-grade gliomas (pHGGs) are a group of tumors affecting approximately 0.85 children per 100,000 annually. The general outcome for these tumors is poor with 5-year survival rates of less than 20%. It is now recognized that these tumors represent a heterogeneous group of tumors rather than one entity. Large-scale genomic analyses have led to a greater understanding of the molecular drivers of different subtypes of these tumors and have also aided in the development of subtype-specific therapies. For example, for pHGG with NTRK fusions, promising new targeted therapies are actively being explored. Herein, we review the clinico-pathologic and molecular classification of these tumors, historical treatments, current management strategies, and therapies currently under investigation.Entities:
Keywords: Glioblastoma; Molecular classification; Pediatric hemispheric high-grade glioma; Targeted therapy
Year: 2020 PMID: 31989507 DOI: 10.1007/s10555-020-09850-5
Source DB: PubMed Journal: Cancer Metastasis Rev ISSN: 0167-7659 Impact factor: 9.264