Cenobamate Efficacy in Individuals With Autoimmune Epilepsy

In recent decades, multiple neuronal autoantibodies directed against cell-surface or intracellular antigens associated with epilepsy and/or encephalopathy have been discovered [2]. Some patients with immune-mediated brain diseases experience seizures that become chronic and are resistant to both antiseizure medications (ASMs) and immunotherapy. This occurs more frequently in patients with antibodies directed against glutamic acid decarboxylase 65 (GAD65) and against onconeural proteins (e.g., Hu, Ma2, collapsing response mediator protein 5/CV2). In this context, the persistence of seizures despite immunotherapy suggests a lasting predisposition, consistent with the current conceptual definition of epilepsy [4].

Cenobamate (CNB) is an antiseizure medication (ASM) recently approved for the treatment of focal-onset seizures, with or without secondary generalization, in adult patients with epilepsy inadequately controlled despite a history of treatment with at least two ASMs [5].

CNB has demonstrated broad-spectrum efficacy, exerting its antiseizure effect through a dual mechanism of action. In addition to inhibiting the persistent component of voltage-gated sodium currents, CNB also acts as a non-benzodiazepine positive allosteric modulator of GABAA channels [6].

The efficacy of CNB in the treatment of patients with anti-GAD65 encephalitis has been suggested by a recent retrospective study, hypothetically compensating for the deficit in GABAergic neurotransmission observed in autoimmune encephalitis associated with anti-GAD65 antibodies [7].

Furthermore, other studies have indicated that ASMs that enhance GABA transmission, such as benzodiazepines and barbiturates, may be beneficial in patients with anti-GABAAR encephalitis, whereas sodium channel blockers have demonstrated efficacy in the treatment of LGI1/CASPR2 antibody-associated encephalitis, reducing repetitive neuronal firing through interaction with voltage-gated sodium channels [8].

Primary objective:

To determine the percentage of patients achieving a ≥50% reduction in seizure frequency during the 24 weeks following initiation of cenobamate treatment compared with the pre-treatment baseline.

Secondary objectives:

• To evaluate the proportion of patients achieving a ≥75% and 100% reduction in seizure frequency compared with baseline.
• To evaluate the safety and tolerability of CNB by documenting the frequency and severity of adverse events.
• To analyze the impact of CNB treatment on patients' quality of life using validated scales such as the Clinical Global Impression (CGI) and the Hospital Anxiety and Depression Scale (HADS).
• To examine the efficacy of CNB according to the specific type of antibody associated with autoimmune epilepsy.

Inclusion criteria

• Age >18 years.
• Signed informed consent.
• Diagnosis of autoimmune epilepsy according to the ILAE 2017 criteria.
• Stable treatment regimen with immunotherapy and antiseizure medications (ASMs) during the 3 months preceding the initiation of CNB treatment.

Exclusion criteria

• Diagnosis of familial short QT syndrome.
• Hypersensitivity to CNB or any of its excipients.
• History of severe adverse drug reactions, including DRESS and Stevens-Johnson syndrome.
• Inability to read and write in Italian.
• Pregnant or breastfeeding patients