» Articles » PMID: 37397394

Unlocking the Power of Precision Medicine for Pediatric Low-grade Gliomas: Molecular Characterization for Targeted Therapies with Enhanced Safety and Efficacy

Overview
Journal Front Oncol
Specialty Oncology
Date 2023 Jul 3
PMID 37397394
Authors
Affiliations
Soon will be listed here.
Abstract

In the past decade significant advancements have been made in the discovery of targetable lesions in pediatric low-grade gliomas (pLGGs). These tumors account for 30-50% of all pediatric brain tumors with generally a favorable prognosis. The latest 2021 WHO classification of pLGGs places a strong emphasis on molecular characterization for significant implications on prognosis, diagnosis, management, and the potential target treatment. With the technological advances and new applications in molecular diagnostics, the molecular characterization of pLGGs has revealed that tumors that appear similar under a microscope can have different genetic and molecular characteristics. Therefore, the new classification system divides pLGGs into several distinct subtypes based on these characteristics, enabling a more accurate strategy for diagnosis and personalized therapy based on the specific genetic and molecular abnormalities present in each tumor. This approach holds great promise for improving outcomes for patients with pLGGs, highlighting the importance of the recent breakthroughs in the discovery of targetable lesions.

Citing Articles

How modern treatments have modified the role of surgery in pediatric low-grade glioma.

Boop S, Shimony N, Boop F Childs Nerv Syst. 2024; 40(10):3357-3365.

PMID: 38676718 PMC: 11511694. DOI: 10.1007/s00381-024-06412-w.


Pediatric CNS tumors and 2021 WHO classification: what do oncologists need from pathologists?.

dAmati A, Bargiacchi L, Rossi S, Carai A, Bertero L, Barresi V Front Mol Neurosci. 2024; 17:1268038.

PMID: 38544524 PMC: 10966132. DOI: 10.3389/fnmol.2024.1268038.

References
1.
Coutant M, Lhermitte B, Guerin E, Chammas A, Reita D, Sebastia C . Retrospective and integrative analyses of molecular characteristics and their specific imaging parameters in pediatric grade 1 gliomas. Pediatr Blood Cancer. 2022; 69(8):e29575. DOI: 10.1002/pbc.29575. View

2.
Yu J, Deshmukh H, Gutmann R, Emnett R, Rodriguez F, Watson M . Alterations of BRAF and HIPK2 loci predominate in sporadic pilocytic astrocytoma. Neurology. 2009; 73(19):1526-31. PMC: 2777068. DOI: 10.1212/WNL.0b013e3181c0664a. View

3.
Nicolaides T, Nazemi K, Crawford J, Kilburn L, Minturn J, Gajjar A . Phase I study of vemurafenib in children with recurrent or progressive BRAF mutant brain tumors: Pacific Pediatric Neuro-Oncology Consortium study (PNOC-002). Oncotarget. 2020; 11(21):1942-1952. PMC: 7260122. DOI: 10.18632/oncotarget.27600. View

4.
Del Bufalo F, Carai A, Figa-Talamanca L, Pettorini B, Mallucci C, Giangaspero F . Response of recurrent BRAFV600E mutated ganglioglioma to Vemurafenib as single agent. J Transl Med. 2014; 12:356. PMC: 4279809. DOI: 10.1186/s12967-014-0356-1. View

5.
Pfister S, Janzarik W, Remke M, Ernst A, Werft W, Becker N . BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas. J Clin Invest. 2008; 118(5):1739-49. PMC: 2289793. DOI: 10.1172/JCI33656. View