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

被引:8
|
作者
Schmitz, Bettina [1 ]
Lattanzi, Simona [2 ]
Vonck, Kristl [3 ]
Kalviainen, Reetta [4 ,5 ]
Nashef, Lina [6 ]
Ben-Menachem, Elinor [7 ]
机构
[1] Vivantes Humboldt Klinikum, Dept Neurol, Ctr Epilepsy, Berlin, Germany
[2] Marche Polytech Univ, Dept Expt & Clin Med, Neurol Clin, Ancona, Italy
[3] Ghent Univ Hosp, Dept Neurol, 4Brain, Ghent, Belgium
[4] Univ Eastern Finland, Kuopio Univ Hosp, Kuopio Epilepsy Ctr, ERN EpiCARE, Kuopio, Finland
[5] Univ Eastern Finland, Inst Clin Med, Kuopio, Finland
[6] Kings Coll Hosp London, Dept Neurol, London, England
[7] Univ Goteborg, Sahlgrenska Acad, Inst Clin Neurosci, Gothenburg, Sweden
关键词
anti-seizure medications; cenobamate; drug resistant epilepsy; epilepsy polytherapy; epilepsy surgery; ketogenic diet; neurostimulation; VAGUS-NERVE-STIMULATION; FOCAL EPILEPSY; ADJUNCTIVE CENOBAMATE; NATURAL-HISTORY; ILAE COMMISSION; DOUBLE-BLIND; DRUG LOAD; SEIZURES; THERAPY; LAMOTRIGINE;
D O I
10.1002/epi4.12830
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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 GABAA 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.
引用
收藏
页码:1241 / 1255
页数:15
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