Targeted Therapy for BRAF Mutant Brain Tumors.


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
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

105

Informations de copyright

© 2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Auteurs

Appaji Rayi (A)

Department of Neurology, Charleston Area Medical Center, Charleston, WV, USA.

Iyad Alnahhas (I)

Division of Neuro-Oncology, Department of Neurology, Thomas Jefferson University, Philadelphia, PA, USA.

Shirley Ong (S)

Division of Neuro-Oncology, Department of Neurology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

Pierre Giglio (P)

Division of Neuro-Oncology, Department of Neurology, The Ohio State University Wexner Medical Center, Columbus, OH, USA.

Vinay K Puduvalli (VK)

Department of Neuro-Oncology, MD Anderson Cancer Center, 1515 Holcombe Blvd, Unit 431, Houston, TX, 77030, USA. vpuduval@mdanderson.org.

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Classifications MeSH