Cenobamate as an Early Adjunctive Treatment in Drug-Resistant Focal-Onset Seizures: An Observational Cohort Study

被引:15
作者
Winter, Yaroslav [1 ,2 ]
Dargham, Raya Abou [1 ]
Tobon, Susana Patino [1 ]
Groppa, Sergiu [3 ]
Fuest, Sven [4 ]
机构
[1] Johannes Gutenberg Univ Mainz, Mainz Comprehens Epilepsy & Sleep Med Ctr, Univ Med Ctr, Dept Neurol, Langenbeck str 1, D-55131 Mainz, Germany
[2] Philipps Univ Marburg, Dept Neurol, Marburg, Germany
[3] Johannes Gutenberg Univ Mainz, Dept Neurol Focus Program Translat Neurosci FTN, Univ Med Ctr, Rhine Main Neurosci Network, Mainz, Germany
[4] Hephata Klin, Dept Neurol, Schwalmstadt, Germany
关键词
SUDDEN UNEXPECTED DEATH; ANTIEPILEPTIC DRUGS; ILAE COMMISSION; EPILEPSY; EFFICACY; SAFETY; TOLERABILITY; RATES;
D O I
10.1007/s40263-024-01109-9
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Objectives Cenobamate (CNB) is a new antiseizure medication (ASM) to treat drug-resistant, focal-onset seizures. Data on its use in early therapy lines are not yet available, and clinicians frequently consider CNB to be a later ASM drug choice. We investigated the efficacy and safety of CNB as an early adjunctive treatment in drug-resistant, focal-onset seizures. Methods The study population were patients with drug-resistant, focal-onset seizures who were initiated with CNB after they did not respond to two or three lifetime ASMs, including all prior and concomitant ASMs. These patients were matched (1:2) by sex, age, and seizure frequency to controls who were initiated with any ASM other than CNB. All participants participated in the Mainz Epilepsy Registry. We evaluated the retention rate after 12 months of CNB and after each new adjunctive ASM in the control group. In addition, seizure freedom and the response rate (reduction of seizure frequency by >= 50% from baseline) after 12 months were estimated. Results We included 231 patients aged 44.4 +/- 15.8 years. Of these, 33.3% (n = 77) were on CNB, 19.0% (n = 44) on valproate (VPA), 17.3% (n = 40) on lacosamide (LCS), 16.4% (n = 38) on levetiracetam (LEV), and 13.9% (n = 32) on topiramate (TPM). The highest retention rate after 12 months since the beginning of the early adjunctive therapy was observed on CNB (92.0%), compared with LCS (80.0%), LEV (73.3%), VPA (68.2%), or TPM (62.5%) (p < 0.05). Seizure freedom and response rate were also the best on CNB (19.5% and 71.4%, respectively) compared with other ASMs (8.3% and 52.5%, respectively; p < 0.05). No significant differences in adverse events between CNB and other ASMs were observed. Conclusions Our study provides evidence that CNB is an effective ASM with a good safety profile in the early therapy lines of drug-resistant, focal-onset seizures. This data should support medical decision making in the management of patients with refractory epilepsy.
引用
收藏
页码:733 / 742
页数:10
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