TY - JOUR
T1 - Resistance, rebound, and recurrence regrowth patterns in pediatric low-grade glioma treated by MAPK inhibition
T2 - A modified Delphi approach to build international consensus-based definitions - International Pediatric Low-Grade Glioma Coalition
AU - O'Hare, Patricia
AU - Cooney, Tabitha
AU - De Blank, Peter
AU - Gutmann, David H.
AU - Kieran, Mark
AU - Milde, Till
AU - Fangusaro, Jason
AU - Fisher, Michael
AU - Avula, Shivaram
AU - Packer, Roger
AU - Fukuoka, Kohei
AU - Mankad, Kshitij
AU - Mueller, Sabine
AU - Waanders, Angela J.
AU - Opocher, Enrico
AU - Bouffet, Eric
AU - Raabe, Eric
AU - Werle, Natacha Entz
AU - Azizi, Amedeo A.
AU - Robison, Nathan J.
AU - Hernáiz Driever, Pablo
AU - Russo, Mark
AU - Schouten, Netteke
AU - Van Tilburg, Cornelis M.
AU - Sehested, Astrid
AU - Grill, Jacques
AU - Bandopadhayay, Pratiti
AU - Kilday, John Paul
AU - Witt, Olaf
AU - Ashley, David M.
AU - Ertl-Wagner, Birgit Betina
AU - Tabori, Uri
AU - Hargrave, Darren R.
N1 - Publisher Copyright:
© 2024 The Author(s).
PY - 2024/8/1
Y1 - 2024/8/1
N2 - 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.
AB - 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.
KW - MAPK
KW - child
KW - low-grade glioma
KW - pediatric brain tumor
KW - rebound
KW - recurrence
KW - resistance
UR - http://www.scopus.com/inward/record.url?scp=85200731015&partnerID=8YFLogxK
U2 - 10.1093/neuonc/noae074
DO - 10.1093/neuonc/noae074
M3 - Review article
C2 - 38743009
AN - SCOPUS:85200731015
SN - 1522-8517
VL - 26
SP - 1357
EP - 1366
JO - Neuro-Oncology
JF - Neuro-Oncology
IS - 8
ER -