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Resistance, rebound, and recurrence regrowth patterns in pediatric low-grade glioma treated by MAPK inhibition: A modified Delphi approach to build international consensus-based definitions-International Pediatric Low-Grade Glioma Coalition.

Authors :
O'Hare P
Cooney T
de Blank P
Gutmann DH
Kieran M
Milde T
Fangusaro J
Fisher M
Avula S
Packer R
Fukuoka K
Mankad K
Mueller S
Waanders AJ
Opocher E
Bouffet E
Raabe E
Werle NE
Azizi AA
Robison NJ
Hernáiz Driever P
Russo M
Schouten N
van Tilburg CM
Sehested A
Grill J
Bandopadhayay P
Kilday JP
Witt O
Ashley DM
Ertl-Wagner BB
Tabori U
Hargrave DR
Source :
Neuro-oncology [Neuro Oncol] 2024 Aug 05; Vol. 26 (8), pp. 1357-1366.
Publication Year :
2024

Abstract

Pediatric low-grade glioma (pLGG) is the most common childhood brain tumor group. The natural history, when curative resection is not possible, is one of a chronic disease with periods of tumor stability and episodes of tumor progression. While there is a high overall survival rate, many patients experience significant and potentially lifelong morbidities. The majority of pLGGs have an underlying activation of the RAS/MAPK pathway due to mutational events, leading to the use of molecularly targeted therapies in clinical trials, with recent regulatory approval for the combination of BRAF and MEK inhibition for BRAFV600E mutated pLGG. Despite encouraging activity, tumor regrowth can occur during therapy due to drug resistance, off treatment as tumor recurrence, or as reported in some patients as a rapid rebound growth within 3 months of discontinuing targeted therapy. Definitions of these patterns of regrowth have not been well described in pLGG. For this reason, the International Pediatric Low-Grade Glioma Coalition, a global group of physicians and scientists, formed the Resistance, Rebound, and Recurrence (R3) working group to study resistance, rebound, and recurrence. A modified Delphi approach was undertaken to produce consensus-based definitions and recommendations for regrowth patterns in pLGG with specific reference to targeted therapies.<br /> (© The Author(s) 2024. Published by Oxford University Press on behalf of the Society for Neuro-Oncology.)

Details

Language :
English
ISSN :
1523-5866
Volume :
26
Issue :
8
Database :
MEDLINE
Journal :
Neuro-oncology
Publication Type :
Academic Journal
Accession number :
38743009
Full Text :
https://doi.org/10.1093/neuonc/noae074