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Cenobamate in refractory epilepsy: Overview of treatment options and practical considerations

Management of drug resistant epilepsy (DRE) represents a challenge to the treating clinician. This manuscript addresses DRE and provides an overview of treatment options, medical, surgical, and dietary. It addresses treatment strategies in polytherapy, then focuses on the role cenobamate (CNB) may p...

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Autores principales: Schmitz, Bettina, Lattanzi, Simona, Vonck, Kristl, Kälviäinen, Reetta, Nashef, Lina, Ben‐Menachem, Elinor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690671/
https://www.ncbi.nlm.nih.gov/pubmed/37743544
http://dx.doi.org/10.1002/epi4.12830
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author Schmitz, Bettina
Lattanzi, Simona
Vonck, Kristl
Kälviäinen, Reetta
Nashef, Lina
Ben‐Menachem, Elinor
author_facet Schmitz, Bettina
Lattanzi, Simona
Vonck, Kristl
Kälviäinen, Reetta
Nashef, Lina
Ben‐Menachem, Elinor
author_sort Schmitz, Bettina
collection PubMed
description Management of drug resistant epilepsy (DRE) represents a challenge to the treating clinician. This manuscript addresses DRE and provides an overview of treatment options, medical, surgical, and dietary. It addresses treatment strategies in polytherapy, then focuses on the role cenobamate (CNB) may play in reducing the burden of DRE while providing practical advice for its introduction. CNB is a recently approved, third generation, anti‐seizure medication (ASM), a tetrazole‐derived carbamate, thought to have a dual mechanism of action, through its effect on sodium channels as well as on GABA(A) receptors at a non‐benzodiazepine site. CNB, having a long half‐life, is an effective add‐on ASM in refractory focal epilepsy with a higher response rate and a higher seizure‐freedom rate than is usually seen in regulatory clinical trials. Experience post‐licensing, though still limited, supports the findings of clinical trials and is encouraging. Its spectrum of action in relation to generalized epilepsies and seizures remains to be established, and there are no data on its efficacy in monotherapy. At the time of writing, CNB has been prescribed for some 50 000 individuals with DRE and focal epilepsy. A larger number is needed to fully establish its safety profile. It should at all times be introduced slowly to minimize the risk of serious allergic drug reactions. It has clinically meaningful interactions which must be anticipated and managed to maximize tolerability and likelihood of successful treatment. Despite the above, it may well prove to be of major benefit in the treatment of many patients with drug resistant epilepsy.
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spelling pubmed-106906712023-12-02 Cenobamate in refractory epilepsy: Overview of treatment options and practical considerations Schmitz, Bettina Lattanzi, Simona Vonck, Kristl Kälviäinen, Reetta Nashef, Lina Ben‐Menachem, Elinor Epilepsia Open Critical Reviews Management of drug resistant epilepsy (DRE) represents a challenge to the treating clinician. This manuscript addresses DRE and provides an overview of treatment options, medical, surgical, and dietary. It addresses treatment strategies in polytherapy, then focuses on the role cenobamate (CNB) may play in reducing the burden of DRE while providing practical advice for its introduction. CNB is a recently approved, third generation, anti‐seizure medication (ASM), a tetrazole‐derived carbamate, thought to have a dual mechanism of action, through its effect on sodium channels as well as on GABA(A) receptors at a non‐benzodiazepine site. CNB, having a long half‐life, is an effective add‐on ASM in refractory focal epilepsy with a higher response rate and a higher seizure‐freedom rate than is usually seen in regulatory clinical trials. Experience post‐licensing, though still limited, supports the findings of clinical trials and is encouraging. Its spectrum of action in relation to generalized epilepsies and seizures remains to be established, and there are no data on its efficacy in monotherapy. At the time of writing, CNB has been prescribed for some 50 000 individuals with DRE and focal epilepsy. A larger number is needed to fully establish its safety profile. It should at all times be introduced slowly to minimize the risk of serious allergic drug reactions. It has clinically meaningful interactions which must be anticipated and managed to maximize tolerability and likelihood of successful treatment. Despite the above, it may well prove to be of major benefit in the treatment of many patients with drug resistant epilepsy. John Wiley and Sons Inc. 2023-10-03 /pmc/articles/PMC10690671/ /pubmed/37743544 http://dx.doi.org/10.1002/epi4.12830 Text en © 2023 The Authors. Epilepsia Open published by Wiley Periodicals LLC on behalf of International League Against Epilepsy. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Critical Reviews
Schmitz, Bettina
Lattanzi, Simona
Vonck, Kristl
Kälviäinen, Reetta
Nashef, Lina
Ben‐Menachem, Elinor
Cenobamate in refractory epilepsy: Overview of treatment options and practical considerations
title Cenobamate in refractory epilepsy: Overview of treatment options and practical considerations
title_full Cenobamate in refractory epilepsy: Overview of treatment options and practical considerations
title_fullStr Cenobamate in refractory epilepsy: Overview of treatment options and practical considerations
title_full_unstemmed Cenobamate in refractory epilepsy: Overview of treatment options and practical considerations
title_short Cenobamate in refractory epilepsy: Overview of treatment options and practical considerations
title_sort cenobamate in refractory epilepsy: overview of treatment options and practical considerations
topic Critical Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10690671/
https://www.ncbi.nlm.nih.gov/pubmed/37743544
http://dx.doi.org/10.1002/epi4.12830
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