Targeted Therapy for BRAF Mutant Brain Tumors.
Alleles
Amino Acid Substitution
Biomarkers, Tumor
Brain Neoplasms
/ diagnosis
Clinical Trials as Topic
Diagnosis, Differential
Disease Management
Disease Susceptibility
Drug Resistance, Neoplasm
/ genetics
Genetic Predisposition to Disease
Genotype
Humans
Molecular Targeted Therapy
/ adverse effects
Mutation
Prognosis
Protein Kinase Inhibitors
/ pharmacology
Proto-Oncogene Proteins B-raf
/ antagonists & inhibitors
Retreatment
Treatment Outcome
Journal
Current treatment options in oncology
ISSN: 1534-6277
Titre abrégé: Curr Treat Options Oncol
Pays: United States
ID NLM: 100900946
Informations de publication
Date de publication:
06 10 2021
06 10 2021
Historique:
accepted:
16
07
2021
entrez:
6
10
2021
pubmed:
7
10
2021
medline:
19
2
2022
Statut:
epublish
Résumé
Molecular heterogeneity has confounded attempts to target individual pathways in brain tumors. However, gliomas with BRAF mutations have been identified as being uniquely vulnerable to targeted therapies. Such mutations are predominantly seen in brain tumors of the adolescent and young adult population. Given that accurate and timely identification of such mutations is essential for offering appropriate treatment, treatment centers should offer both immunohistochemical and sequencing methods for detection of these mutations to guide treatment. Additional studies of these tumors at recurrence would also allow identification of breakthrough resistance mechanisms that may also be targetable for treatment. Due to the relative rarity of these tumors, multicenter collaborative studies will be essential in achieving long term control of these tumors.
Identifiants
pubmed: 34613491
doi: 10.1007/s11864-021-00901-9
pii: 10.1007/s11864-021-00901-9
doi:
Substances chimiques
Biomarkers, Tumor
0
Protein Kinase Inhibitors
0
BRAF protein, human
EC 2.7.11.1
Proto-Oncogene Proteins B-raf
EC 2.7.11.1
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
105Informations de copyright
© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.