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Challenges of targeting BRAF V600E mutations in adult primary brain tumor patients: a report of two cases

AIM: Therapeutic targeting of BRAF alterations in primary brain tumor patients has demonstrated clinical activity in case reports and early trials; however, there is limited high-level evidence of the efficacy. PATIENTS & RESULTS: Targeting BRAF V600E mutations with concurrent dabrafenib and tra...

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Autores principales: Smith-Cohn, Matthew, Davidson, Christian, Colman, Howard, Cohen, Adam L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912849/
https://www.ncbi.nlm.nih.gov/pubmed/31818130
http://dx.doi.org/10.2217/cns-2019-0018
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author Smith-Cohn, Matthew
Davidson, Christian
Colman, Howard
Cohen, Adam L
author_facet Smith-Cohn, Matthew
Davidson, Christian
Colman, Howard
Cohen, Adam L
author_sort Smith-Cohn, Matthew
collection PubMed
description AIM: Therapeutic targeting of BRAF alterations in primary brain tumor patients has demonstrated clinical activity in case reports and early trials; however, there is limited high-level evidence of the efficacy. PATIENTS & RESULTS: Targeting BRAF V600E mutations with concurrent dabrafenib and trametinib in anaplastic pleomorphic xanthoastrocytoma resulted in a transient radiographic and clinical response and no therapeutic benefit in a patient with an epithelioid glioblastoma. CONCLUSION: BRAF/MEK inhibition did not produce a durable treatment effect in glioblastoma or pleomorphic xanthoastrocytoma with BRAF V600E alterations. Heterogenicity of related cases in the literature makes an evaluation of efficacy BRAF targeting therapies in gliomas difficult and requires additional investigation.
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spelling pubmed-69128492019-12-17 Challenges of targeting BRAF V600E mutations in adult primary brain tumor patients: a report of two cases Smith-Cohn, Matthew Davidson, Christian Colman, Howard Cohen, Adam L CNS Oncol Case Series AIM: Therapeutic targeting of BRAF alterations in primary brain tumor patients has demonstrated clinical activity in case reports and early trials; however, there is limited high-level evidence of the efficacy. PATIENTS & RESULTS: Targeting BRAF V600E mutations with concurrent dabrafenib and trametinib in anaplastic pleomorphic xanthoastrocytoma resulted in a transient radiographic and clinical response and no therapeutic benefit in a patient with an epithelioid glioblastoma. CONCLUSION: BRAF/MEK inhibition did not produce a durable treatment effect in glioblastoma or pleomorphic xanthoastrocytoma with BRAF V600E alterations. Heterogenicity of related cases in the literature makes an evaluation of efficacy BRAF targeting therapies in gliomas difficult and requires additional investigation. Future Medicine Ltd 2019-10-06 /pmc/articles/PMC6912849/ /pubmed/31818130 http://dx.doi.org/10.2217/cns-2019-0018 Text en © 2019 Matthew Smith-Cohn This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Case Series
Smith-Cohn, Matthew
Davidson, Christian
Colman, Howard
Cohen, Adam L
Challenges of targeting BRAF V600E mutations in adult primary brain tumor patients: a report of two cases
title Challenges of targeting BRAF V600E mutations in adult primary brain tumor patients: a report of two cases
title_full Challenges of targeting BRAF V600E mutations in adult primary brain tumor patients: a report of two cases
title_fullStr Challenges of targeting BRAF V600E mutations in adult primary brain tumor patients: a report of two cases
title_full_unstemmed Challenges of targeting BRAF V600E mutations in adult primary brain tumor patients: a report of two cases
title_short Challenges of targeting BRAF V600E mutations in adult primary brain tumor patients: a report of two cases
title_sort challenges of targeting braf v600e mutations in adult primary brain tumor patients: a report of two cases
topic Case Series
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6912849/
https://www.ncbi.nlm.nih.gov/pubmed/31818130
http://dx.doi.org/10.2217/cns-2019-0018
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