학술논문

Molecular classification and outcome of children with rare CNS embryonal tumors: results from St. Jude Childrens Research Hospital including the multi-center SJYC07 and SJMB03 clinical trials.
Document Type
article
Source
Acta Neuropathologica. 144(4)
Subject
Brain Neoplasms
Central Nervous System Neoplasms
Child
Forkhead Transcription Factors
Glioblastoma
Hospitals
Humans
Neoplasms
Germ Cell and Embryonal
Neuroectodermal Tumors
Primitive
Language
Abstract
Methylation profiling has radically transformed our understanding of tumors previously called central nervous system primitive neuro-ectodermal tumors (CNS-PNET). While this marks a momentous step toward defining key differences, reclassification has thrown treatment into disarray. To shed light on response to therapy and guide clinical decision-making, we report outcomes and molecular features of children with CNS-PNETs from two multi-center risk-adapted studies (SJMB03 for patients ≥ 3 years; SJYC07 for patients