ABSTRACT
Introduction
Focal seizures represent the most common seizure type and focal epilepsies the most common epilepsy type. Anti-seizure medications (ASMs) still represent the main form of treatment for epilepsy.
Areas covered
The aim of this review article is to provide an overview of available evidence about current and upcoming pharmacological options and strategies for adults with focal epilepsy focusing on the last 5 years.
Expert opinion
Seventeen drugs are currently approved for the treatment of focal seizures including cenobamate as the very latest option. Ten of these drugs are also licensed for monotherapy. Level A evidence for initial monotherapy is available for seven drugs with no robust data supporting that one drug is superior to the other. Safety, tolerability as well as pharmacoeconomic reasons would then drive treatment decisions. Data on adjunctive treatment are available for 13 ASMs showing again no obvious difference in terms of efficacy. Evidence on specific drug combinations is almost non-existent and the final decision of combining specific drugs is based on the experience of the individual clinician rather than on robust evidence. Current outcome measures do not consider number of previously failed drugs and the observation period is often too short.
Article highlights
Seventeen drugs are currently licensed for the treatment of focal seizures
Level A of evidence for the initial monotherapy of focal seizures is available for seven drugs with no difference in terms of efficacy
Data on adjunctive treatment are available for 13 drugs with no difference in terms of efficacy
Lamotrigine and levetiracetam represent the best options when efficacy safety and tolerability are considered
Evidence of specific drug combinations is non-existent and clinical practice is based on the experience of the individual clinician
Head-to-head comparison studies using appropriate outcome measures are needed
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Declaration of interest
M Mula has received personal fees from UCB, Eisai, Bial, and Elsevier all outside the submitted work. Furthermore, M Mula has intellectual property rights with Springer and Elsevier. He has no other relevant affiliations or financial involvement with any organization or entity with a financial interest in or financial conflict with the subject matter or materials discussed in the manuscript apart from those disclosed.
Reviewer disclosures
Peer reviewers on this manuscript have no relevant financial or other relationships to disclose.