TY - JOUR
T1 - Consensus framework for conducting phase I/II clinical trials for children, adolescents, and young adults with pediatric low-grade glioma
T2 - Guidelines established by the International Pediatric Low-Grade Glioma Coalition Clinical Trial Working Group
AU - Mueller, Sabine
AU - Fangusaro, Jason
AU - Thomas, Arzu Onar
AU - Jacques, Thomas S
AU - Bandopadhayay, Pratiti
AU - de Blank, Peter
AU - Packer, Roger J
AU - Fouladi, Maryam
AU - van Meeteren, Antoinette Schouten
AU - Jones, David
AU - Perry, Arie
AU - Nakano, Yoshiko
AU - Hargrave, Darren
AU - Riedl, David
AU - Robinson, Nathan J
AU - Partanen, Marita
AU - Fisher, Michael J
AU - Witt, Olaf
N1 - © 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 - 2023/12/26
Y1 - 2023/12/26
N2 - Within the last few decades, we have witnessed tremendous advancements in the study of pediatric low-grade gliomas (pLGG), leading to a much-improved understanding of their molecular underpinnings. Consequently, we have achieved successful milestones in developing and implementing targeted therapeutic agents for treating these tumors. However, the community continues to face many unknowns when it comes to the most effective clinical implementation of these novel targeted inhibitors or combinations thereof. Questions encompassing optimal dosing strategies, treatment duration, methods for assessing clinical efficacy, and the identification of predictive biomarkers remain unresolved. Here, we offer the consensus of the international pLGG coalition (iPLGGc) clinical trial working group on these important topics and comment on clinical trial design and endpoint rationale. Throughout, we seek to standardize the global approach to early clinical trials (phase I and II) for pLGG, leading to more consistently interpretable results as well as enhancing the pace of novel therapy development and encouraging an increased focus on functional endpoints as well and quality of life for children faced with this disease.
AB - Within the last few decades, we have witnessed tremendous advancements in the study of pediatric low-grade gliomas (pLGG), leading to a much-improved understanding of their molecular underpinnings. Consequently, we have achieved successful milestones in developing and implementing targeted therapeutic agents for treating these tumors. However, the community continues to face many unknowns when it comes to the most effective clinical implementation of these novel targeted inhibitors or combinations thereof. Questions encompassing optimal dosing strategies, treatment duration, methods for assessing clinical efficacy, and the identification of predictive biomarkers remain unresolved. Here, we offer the consensus of the international pLGG coalition (iPLGGc) clinical trial working group on these important topics and comment on clinical trial design and endpoint rationale. Throughout, we seek to standardize the global approach to early clinical trials (phase I and II) for pLGG, leading to more consistently interpretable results as well as enhancing the pace of novel therapy development and encouraging an increased focus on functional endpoints as well and quality of life for children faced with this disease.
U2 - 10.1093/neuonc/noad227
DO - 10.1093/neuonc/noad227
M3 - Article
C2 - 38146999
SN - 1522-8517
JO - Neuro-Oncology
JF - Neuro-Oncology
ER -