TY - JOUR
T1 - Updated EANO guideline on rational molecular testing of gliomas, glioneuronal, and neuronal tumors in adults for targeted therapy selection - Update 1
AU - Van Den Bent, Martin J.
AU - Franceschi, Enrico
AU - Touat, Mehdi
AU - French, Pim J.
AU - Idbaih, Ahmed
AU - Lombardi, Giuseppe
AU - Rudà, Roberta
AU - Schweizer, Leonille
AU - Capper, David
AU - Sanson, Marc
AU - Wesseling, Pieter
AU - Weller, Michael
AU - Eoli, Marica
AU - Anghileri, Elena
AU - Bielle, Franck
AU - Euskirchen, Phillipp
AU - Geurts, Marjolein
AU - Wen, Patrick Y.
AU - Preusser, Matthias
N1 - Publisher Copyright:
© 2024 The Author(s).
PY - 2025/2
Y1 - 2025/2
N2 - The standard of care for adult patients with gliomas, glioneuronal, and neuronal tumors consists of combinations of surgery, radiotherapy, and chemotherapy. For many systemic cancers, targeted treatments are a major part of the standard treatment; however, the predictive significance of most of the targets for treatment in systemic cancer is less well-established in central nervous system tumors. In 2023 the European Association for NeuroOncology (EANO) Guideline Committee presented evidence-based recommendations for rational testing of molecular targets for targeted treatments. From all targets reviewed, only testing for BRAF V600E mutations was of proven clinical benefit; despite regulatory approvals for tumor agnostic treatment of NTRK gene fusions and high tumor mutational burden (TMB) for patients with adult brain tumors, the evidence of clinical benefit for adult patients was still limited. This guideline has a modular structure, allowing regular updating of individual sections and adding new ones. The present version (Update 1) presents a review of the rationale of testing for PTEN, H3F3A, MTAP, RET and IDH, and presents an update of the text on TMB high and mismatch repair deficiency. It also presents an overview of the therapeutic yield of routine next-generation sequencing for mutations and fusion detection. The Supplemental File II accompanying this version contains an in-depth review of all targets, whereas, in the main manuscript, the final recommendations of the revised and new targets are presented. Updates will be made on a regular basis.
AB - The standard of care for adult patients with gliomas, glioneuronal, and neuronal tumors consists of combinations of surgery, radiotherapy, and chemotherapy. For many systemic cancers, targeted treatments are a major part of the standard treatment; however, the predictive significance of most of the targets for treatment in systemic cancer is less well-established in central nervous system tumors. In 2023 the European Association for NeuroOncology (EANO) Guideline Committee presented evidence-based recommendations for rational testing of molecular targets for targeted treatments. From all targets reviewed, only testing for BRAF V600E mutations was of proven clinical benefit; despite regulatory approvals for tumor agnostic treatment of NTRK gene fusions and high tumor mutational burden (TMB) for patients with adult brain tumors, the evidence of clinical benefit for adult patients was still limited. This guideline has a modular structure, allowing regular updating of individual sections and adding new ones. The present version (Update 1) presents a review of the rationale of testing for PTEN, H3F3A, MTAP, RET and IDH, and presents an update of the text on TMB high and mismatch repair deficiency. It also presents an overview of the therapeutic yield of routine next-generation sequencing for mutations and fusion detection. The Supplemental File II accompanying this version contains an in-depth review of all targets, whereas, in the main manuscript, the final recommendations of the revised and new targets are presented. Updates will be made on a regular basis.
UR - http://www.scopus.com/inward/record.url?scp=85218168801&partnerID=8YFLogxK
U2 - 10.1093/neuonc/noae213
DO - 10.1093/neuonc/noae213
M3 - Review article
C2 - 39387386
AN - SCOPUS:85218168801
SN - 1522-8517
VL - 27
SP - 331
EP - 337
JO - Neuro-Oncology
JF - Neuro-Oncology
IS - 2
ER -