» Articles » PMID: 38743009

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

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.

Citing Articles

Current clinical trials for craniopharyngiomas: what's on the horizon?.

Joshi N, Mueller S, Kline C J Neurooncol. 2025; .

PMID: 40042714 DOI: 10.1007/s11060-024-04899-6.


BRAF/MEK inhibitors use for pediatric gliomas; real world experience from a resource-limited country.

Abu Laban D, Alsharif A, Al-Hussaini M, Obeidat M, Maraqa B, Alzoubi Q Front Oncol. 2024; 14:1417484.

PMID: 39399174 PMC: 11466720. DOI: 10.3389/fonc.2024.1417484.

References
1.
Robert C, Grob J, Stroyakovskiy D, Karaszewska B, Hauschild A, Levchenko E . Five-Year Outcomes with Dabrafenib plus Trametinib in Metastatic Melanoma. N Engl J Med. 2019; 381(7):626-636. DOI: 10.1056/NEJMoa1904059. View

2.
Oxnard G, Morris M, Hodi F, Baker L, Kris M, Venook A . When progressive disease does not mean treatment failure: reconsidering the criteria for progression. J Natl Cancer Inst. 2012; 104(20):1534-41. PMC: 3708548. DOI: 10.1093/jnci/djs353. View

3.
Jones D, Kieran M, Bouffet E, Alexandrescu S, Bandopadhayay P, Bornhorst M . Pediatric low-grade gliomas: next biologically driven steps. Neuro Oncol. 2017; 20(2):160-173. PMC: 5786244. DOI: 10.1093/neuonc/nox141. View

4.
Yamazaki H, Sugino K, Matsuzu K, Masaki C, Akaishi J, Hames K . Rapid disease progression after discontinuation of lenvatinib in thyroid cancer. Medicine (Baltimore). 2020; 99(11):e19408. PMC: 7220477. DOI: 10.1097/MD.0000000000019408. View

5.
Youssef G, Rahman R, Bay C, Wang W, Lim-Fat M, Arnaout O . Evaluation of Standard Response Assessment in Neuro-Oncology, Modified Response Assessment in Neuro-Oncology, and Immunotherapy Response Assessment in Neuro-Oncology in Newly Diagnosed and Recurrent Glioblastoma. J Clin Oncol. 2023; 41(17):3160-3171. DOI: 10.1200/JCO.22.01579. View