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Perampanel in Brain Tumor-Related Epilepsy: A Systematic Review
Brain tumor-related epilepsy (BTRE) is a common comorbidity in patients with brain neoplasms and it may be either the first symptom or develop after the tumor diagnosis. Increasing evidence suggests that brain tumors and BTRE share common pathophysiological mechanisms. Glutamatergic mechanisms can p...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954094/ https://www.ncbi.nlm.nih.gov/pubmed/36831869 http://dx.doi.org/10.3390/brainsci13020326 |
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author | Tabaee Damavandi, Payam Pasini, Francesco Fanella, Gaia Cereda, Giulia Sofia Mainini, Gabriele DiFrancesco, Jacopo C. Trinka, Eugen Lattanzi, Simona |
author_facet | Tabaee Damavandi, Payam Pasini, Francesco Fanella, Gaia Cereda, Giulia Sofia Mainini, Gabriele DiFrancesco, Jacopo C. Trinka, Eugen Lattanzi, Simona |
author_sort | Tabaee Damavandi, Payam |
collection | PubMed |
description | Brain tumor-related epilepsy (BTRE) is a common comorbidity in patients with brain neoplasms and it may be either the first symptom or develop after the tumor diagnosis. Increasing evidence suggests that brain tumors and BTRE share common pathophysiological mechanisms. Glutamatergic mechanisms can play a central role in promoting both primary brain tumor growth and epileptogenesis. Perampanel (PER), which acts as a selective antagonist of glutamate α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, may play a role both in the reduction in tumor growth and the control of epileptiform activity. This systematic review aimed to summarize the pre-clinical and clinical evidence about the antitumor properties, antiseizure effects and tolerability of PER in BTRE. Eight pre-clinical and eight clinical studies were identified. The currently available evidence suggests that PER can be an effective and generally well-tolerated therapeutic option in patients with BTRE. In vitro studies demonstrated promising antitumor activity of PER, while no role in slowing tumor progression has been demonstrated in rat models; clinical data on the potential antitumor activity of PER are scarce. Additional studies are needed to explore further the effects of PER on tumor progression and fully characterize its potentialities in patients with BTRE. |
format | Online Article Text |
id | pubmed-9954094 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99540942023-02-25 Perampanel in Brain Tumor-Related Epilepsy: A Systematic Review Tabaee Damavandi, Payam Pasini, Francesco Fanella, Gaia Cereda, Giulia Sofia Mainini, Gabriele DiFrancesco, Jacopo C. Trinka, Eugen Lattanzi, Simona Brain Sci Review Brain tumor-related epilepsy (BTRE) is a common comorbidity in patients with brain neoplasms and it may be either the first symptom or develop after the tumor diagnosis. Increasing evidence suggests that brain tumors and BTRE share common pathophysiological mechanisms. Glutamatergic mechanisms can play a central role in promoting both primary brain tumor growth and epileptogenesis. Perampanel (PER), which acts as a selective antagonist of glutamate α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptors, may play a role both in the reduction in tumor growth and the control of epileptiform activity. This systematic review aimed to summarize the pre-clinical and clinical evidence about the antitumor properties, antiseizure effects and tolerability of PER in BTRE. Eight pre-clinical and eight clinical studies were identified. The currently available evidence suggests that PER can be an effective and generally well-tolerated therapeutic option in patients with BTRE. In vitro studies demonstrated promising antitumor activity of PER, while no role in slowing tumor progression has been demonstrated in rat models; clinical data on the potential antitumor activity of PER are scarce. Additional studies are needed to explore further the effects of PER on tumor progression and fully characterize its potentialities in patients with BTRE. MDPI 2023-02-14 /pmc/articles/PMC9954094/ /pubmed/36831869 http://dx.doi.org/10.3390/brainsci13020326 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Tabaee Damavandi, Payam Pasini, Francesco Fanella, Gaia Cereda, Giulia Sofia Mainini, Gabriele DiFrancesco, Jacopo C. Trinka, Eugen Lattanzi, Simona Perampanel in Brain Tumor-Related Epilepsy: A Systematic Review |
title | Perampanel in Brain Tumor-Related Epilepsy: A Systematic Review |
title_full | Perampanel in Brain Tumor-Related Epilepsy: A Systematic Review |
title_fullStr | Perampanel in Brain Tumor-Related Epilepsy: A Systematic Review |
title_full_unstemmed | Perampanel in Brain Tumor-Related Epilepsy: A Systematic Review |
title_short | Perampanel in Brain Tumor-Related Epilepsy: A Systematic Review |
title_sort | perampanel in brain tumor-related epilepsy: a systematic review |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954094/ https://www.ncbi.nlm.nih.gov/pubmed/36831869 http://dx.doi.org/10.3390/brainsci13020326 |
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