TY - JOUR
T1 - EANO guideline on rational molecular testing of gliomas, glioneuronal and neuronal tumors in adults for targeted therapy selection
AU - Capper, David
AU - Reifenberger, Guido
AU - French, Pim J
AU - Schweizer, Leonille
AU - Weller, Michael
AU - Touat, Mehdi
AU - Niclou, Simone P
AU - Euskirchen, Philipp
AU - Haberler, Christine
AU - Hegi, Monika E
AU - Brandner, Sebastian
AU - Le Rhun, Emilie
AU - Rudà, Roberta
AU - Sanson, Marc
AU - Tabatabai, Ghazaleh
AU - Sahm, Felix
AU - Wen, Patrick Y
AU - Wesseling, Pieter
AU - Preusser, Matthias
AU - van den Bent, Martin J
N1 - DC has received research support from Novocure. DC recives royalities for sales of mutation specific antibodies H09 (IDH1 R132H) and VE1 (BRAF V600E). A patent for DNA methylation based tumor profiling has been filed; GR, PJF, have nothing to disclose; LS received honoraria for lectures from Molecular Health; MW has received research grants from Quercis and Versameb, and honoraria for lectures or advisory board participation or consulting from Bayer, Medac, Merck (EMD), Novartis, Orbus, and Philogen; MT has a consulting or advisory role with Servier, Novocure, Integragen, and Taiho Oncology, and research funding from Sanofi; SPN, PE, CH, MH, SB have nothing to disclose; ELR has received a research grant from Bristol Meyer Squibb and honoraria for lectures or advisory board from Adastra, Bayer, Janssen, Leo Pharma, Pierre Fabre, and Seattle Genetics; RR has received honoraria for lectures, consultation or advisory board from UCB, Bayer, Novocure, Genenta; MS reports research support from AstraZeneca, and received honoraria for consultation or advisory from Genenta and Abbvie; GT has served on advisory boards of AbbVie, Bayer, Boehringer Ingelheim, Bristol-Myers Squibb; received consulting fees from AbbVie, Bayer; received speaker fees from Medac and Novocure; FS has received honoraria from Bayer, Illumina ; Patent and royalties thereof for a method for classification of cancer; PYW has received research support from Astra Zeneca/Medimmune, Beigene, Celgene, Chimerix, Eli Lily, Genentech/Roche, Kazia, MediciNova, Merck, Novartis, Nuvation Bio, Puma, Servier, Vascular Biogenics, VBI Vaccines and honoraria for advisory board participation on consultation from Astra Zeneca, Bayer, Black Diamond, Boehringer Ingelheim, Boston Pharmaceuticals, Celularity, Chimerix, Day One Bio, Genenta, Glaxo Smith Kline, Karyopharm, Merck, Mundipharma, Novartis, Novocure, Nuvation Bio, Prelude Therapeutics, Sapience, Servier, Sagimet, Vascular Biogenics, VBI Vaccines; PW has nothing to disclose; MP has received honoraria for lectures, consultation or advisory board participation from the following for-profit companies: Bayer, Bristol-Myers Squibb, Novartis, Gerson Lehrman Group (GLG), CMC Contrast, GlaxoSmithKline, Mundipharma, Roche, BMJ Journals, MedMedia, Astra Zeneca, AbbVie, Lilly, Medahead, Daiichi Sankyo, Sanofi, Merck Sharp & Dome, Tocagen, Adastra, Gan & Lee Pharmaceuticals; MvdB has received honoraria for consultancy or advisory board participation from the following companies: Servier, Boehringer, Carthera, Genenta, Nerviano, Chimerix, Astra Zeneca, Fore Biotherapeutics, and Roche.
© The Author(s) 2023. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. All rights reserved. For permissions, please e-mail: [email protected].
PY - 2023/5/4
Y1 - 2023/5/4
N2 - The mainstay of treatment 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 part of standard of care, however the predictive significance of most of these targets in CNS tumors remains less well studied. Despite that, there is an increasing use of advanced molecular diagnostics that identify potential targets, and tumor agnostic regulatory approvals on targets also present in CNS tumors have been granted. This raises the question when and for which targets it is meaningful to test in adult patients with CNS tumors. This evidence based guideline reviews the evidence available for targeted treatment for alterations in the RAS/MAPK pathway (BRAF, NF1), in growth factor receptors (EGFR, ALK, FGFR, NTRK, PDGFRA, ROS1), in cell cycle signaling (CDK4/6, MDM2/4, TSC1/2) and altered genomic stability (mismatch repair, POLE, high TMB, HRD) in adult patients with gliomas, glioneuronal and neuronal tumors. At present, targeted treatment for BRAF p.V600E alterations is to be considered part of standard of care for patients with recurrent gliomas, pending regulatory approval. For approved tumor agnostic treatments for NTRK fusions and high TMB, the evidence for efficacy in adult patients with CNS tumors is very limited, and treatment should preferably be given within prospective clinical registries and trials. For targeted treatment of CNS tumors with FGFR fusions or mutations, clinical trials are ongoing to confirm modest activity so far observed in basket trials. For all other reviewed targets, evidence of benefit in CNS tumors is currently lacking, and testing/treatment should be in the context of available clinical trials.
AB - The mainstay of treatment 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 part of standard of care, however the predictive significance of most of these targets in CNS tumors remains less well studied. Despite that, there is an increasing use of advanced molecular diagnostics that identify potential targets, and tumor agnostic regulatory approvals on targets also present in CNS tumors have been granted. This raises the question when and for which targets it is meaningful to test in adult patients with CNS tumors. This evidence based guideline reviews the evidence available for targeted treatment for alterations in the RAS/MAPK pathway (BRAF, NF1), in growth factor receptors (EGFR, ALK, FGFR, NTRK, PDGFRA, ROS1), in cell cycle signaling (CDK4/6, MDM2/4, TSC1/2) and altered genomic stability (mismatch repair, POLE, high TMB, HRD) in adult patients with gliomas, glioneuronal and neuronal tumors. At present, targeted treatment for BRAF p.V600E alterations is to be considered part of standard of care for patients with recurrent gliomas, pending regulatory approval. For approved tumor agnostic treatments for NTRK fusions and high TMB, the evidence for efficacy in adult patients with CNS tumors is very limited, and treatment should preferably be given within prospective clinical registries and trials. For targeted treatment of CNS tumors with FGFR fusions or mutations, clinical trials are ongoing to confirm modest activity so far observed in basket trials. For all other reviewed targets, evidence of benefit in CNS tumors is currently lacking, and testing/treatment should be in the context of available clinical trials.
UR - https://pubmed.ncbi.nlm.nih.gov/36632791
U2 - 10.1093/neuonc/noad008
DO - 10.1093/neuonc/noad008
M3 - Article
C2 - 36632791
SN - 1522-8517
VL - 25
SP - 813
EP - 826
JO - Neuro-Oncology
JF - Neuro-Oncology
IS - 5
ER -