4.3 Article

Efficacy and safety of cenobamate in patients with uncontrolled focal seizures: A meta-analysis

Journal

ACTA NEUROLOGICA SCANDINAVICA
Volume 144, Issue 1, Pages 58-66

Publisher

WILEY
DOI: 10.1111/ane.13422

Keywords

adverse event; cenobamate; meta‐ analysis; randomized controlled trial; uncontrolled focal seizures

Funding

  1. Jiangsu Province Maternal and Children Health Project [F201749]
  2. Yancheng Medical Science Development Project [YK2020053]

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This study systematically investigated the efficacy and safety of adjunctive cenobamate for uncontrolled focal seizures, showing that cenobamate had favorable efficacy, especially at the dose of 400 mg, and was well tolerated.
Objective To investigate the efficacy and safety of adjunctive cenobamate for treatment of uncontrolled focal seizures. Methods We performed a systematic search of Web of Science, MEDLINE (Ovid and PubMed), Cochrane Library, EMBASE and Google Scholar to identify eligible studies. We included randomized placebo-controlled trials (RCTs) for uncontrolled focal seizures. We calculated the risk ratio (RR) of >= 50%, >= 75% and 100% reduction in seizure frequency from baseline, as well as dropout and serious adverse events related to treatment. Quality of included trials was assessed using the Cochrane Collaboration's tool. Results Two RCTs with a total of 658 patients were included. A significantly larger proportion of patients allocated to cenobamate achieved 50% seizure reduction (RR 2.06, 95% CI 1.70-2.51, p < 0.001) as compared to placebo, subgroup analysis demonstrated that the most effective dose was at 400 mg (RR 2.28, 95% CI 1.57-3.32, p < 0.001). Patients achieving seizure-freedom during the treatment period were 14.9% with cenobamate and 4.5% with placebo (RR 5.32, 95% CI 2.94-9.62, p < 0.001). Dropouts (RR 1.40, 95% CI 1.01-1.94, p = 0.05) and incidence of serious adverse events (RR 1.48, 95% CI 0.93-2.33, p = 0.1) were not significantly higher in patients receiving cenobamate. However, subgroup analyses based on doses suggested that patients exposed to 400 mg cenobamate were more likely to dropout than placebo (RR 2.09, 95% CI 1.17- 3.71, p = 0.012). Conclusion Cenobamate demonstrated favourable efficacy for treatment of uncontrolled focal seizures and showed a dose-related fashion. Cenobamate could be well tolerated, the most common adverse events associated with cenobamate were dizziness, somnolence, fatigue, headache and nausea. Nevertheless, majority of them were mild to moderate in severity.

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