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Cenobamate as add-on therapy for drug resistant epilepsies: effectiveness, drug to drug interactions and neuropsychological impact. What have we learned from real word evidence?
Pietrafusa, Nicola; Falcicchio, Giovanni; Russo, Emilio; Lattanzi, Simona; Goffredo, Bianca; Simeoli, Raffaele; Cairoli, Sara; Corsetti, Tiziana; Roberti, Roberta; De Tommaso, Marina; Vigevano, Federico; La Neve, Angela; Specchio, Nicola.
Affiliation
  • Pietrafusa N; Clinical and Experimental Neurology, Full Member of European Reference Network EpiCARE, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Falcicchio G; Department of Translational Biomedicine and Neurosciences, University of Bari 'Aldo Moro', Bari, Italy.
  • Russo E; Science of Health Department, University Magna Grecia of Catanzaro, Catanzaro, Italy.
  • Lattanzi S; Neurological Clinic, Department of Experimental and Clinical Medicine, Marche Polytechnic University, Ancona, Italy.
  • Goffredo B; Division of Metabolic Diseases and Drug Biology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Simeoli R; Division of Metabolic Diseases and Drug Biology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Cairoli S; Division of Metabolic Diseases and Drug Biology, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Corsetti T; Hospital Pharmacy Unit, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • Roberti R; Science of Health Department, University Magna Grecia of Catanzaro, Catanzaro, Italy.
  • De Tommaso M; Department of Translational Biomedicine and Neurosciences, University of Bari 'Aldo Moro', Bari, Italy.
  • Vigevano F; Head of Neurological Sciences and Rehabilitation Medicine Scientific Area, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
  • La Neve A; Department of Translational Biomedicine and Neurosciences, University of Bari 'Aldo Moro', Bari, Italy.
  • Specchio N; Clinical and Experimental Neurology, Full Member of European Reference Network EpiCARE, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Front Pharmacol ; 14: 1239152, 2023.
Article in En | MEDLINE | ID: mdl-38186643
ABSTRACT

Background:

Cenobamate (CNB) is an anti-seizure medication (ASM) approved in 2021 in Europe for adjunctive treatment of focal-onset seizures in adults who were not adequately controlled with at least two previous ASMs.

Methods:

seizure outcome, treatment-emergent adverse events, neuropsychological profile, and blood levels of CNB and concomitant ASM were analyzed in a real world setting in two different Italian epilepsy centers in the context of CNB early access program. All patients performed a general cognitive evaluation, while 32 patients underwent the administration of a battery of neuropsychological tests at baseline and 6 months after CNB treatment. We performed CNB quantification in plasma in 31 patients at different doses in the range of 100-400 mg/day (65 measures).

Results:

we enrolled 54 patients with a median age of 27.9 years. The mean follow-up was 10.7 months. Most (91%) completed the efficacy analysis. At last follow-up visit, a 69.5% median seizure reduction was registered. Thirty-two patients (59.2%) had a ≥50% reduction of seizures that was ≥75% in 20 (42.0%) cases, whilst 10 (20.2%) patients were seizure-free. The most common adverse events were somnolence (53.1%), dizziness (28.1%) and diplopia (12.5%). The correlation between CNB dose and plasma concentration, revealed a significant linear correlation (r = 0.86, p < 0.0001), and there was a significant difference in mean plasma concentration/dose administered ratio (C/D ratio) between patients taking or not at least one inducer (0.10 ± 0.04 [(µg/mL)/(mg/day)]; n = 47 vs. 0.13 ± 0.05 [(µg/mL)/(mg/day)]; n = 18, p = 0.04). CNB dose was inversely correlated (r = -0.31, p = 0.02) to the C/D ratio of Carbamazepine blood levels. and positively correlated (r = 0.74, p < 0.0001) with an increased plasma concentration of the active Clobazam metabolite N-desmethylclobazam. General Anxiety Disorder-7 showed a significant improvement of score from baseline evaluation of 6.82 to follow-up 6 months evaluation of 4.53 (p = 0.03).

Conclusion:

In this real-world study, we registered a clinically meaningful reduction in seizure frequency after CNB administration in most patients along with a good tolerability profile. CNB treatment is correlate to a reduction in symptom severity of anxiety score. Plasma levels measurements confirm that CNB acts both as "victim" and as "perpetrator" of drug-drug interactions.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Pharmacol Year: 2023 Document type: Article Affiliation country: Italia Country of publication: Suiza

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Front Pharmacol Year: 2023 Document type: Article Affiliation country: Italia Country of publication: Suiza