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THUR 058 Eslicarbazepine acetate as monotherapy in clinical practice
  1. McMurray Rob1,
  2. Delanty Norman2,
  3. Villanueva Vicente3
  1. 1Eisai Europe Ltd, Hatfield
  2. 2Beaumont Hospital, Dublin, Ireland
  3. 3Hospital Universitario y Politécnico La Fe, Valencia, Spain

Abstract

Purpose To assess eslicarbazepine acetate (ESL) as monotherapy in everyday clinical practice.

Method Euro-Esli was a pooled analysis of 14 European studies. In a subanalysis, data were compared for patients treated initially with ESL monotherapy versus adjunctive therapy, and for patients treated at last visit with ESL monotherapy versus adjunctive therapy.

Assessments included responder rate (≥50% seizure frequency reduction), seizure freedom rate (seizure freedom at least since prior visit) and incidence of adverse events (AEs).

Results ESL was used as monotherapy in 88/2045 and 229/1340 patients initially and at last visit, respectively. At 12 months, responder and seizure freedom rates were significantly higher in patients treated initially with ESL monotherapy versus adjunctive therapy (responder: 94.1% versus 74.8%; seizure freedom: 88.2% versus 39.0%), and in patients treated at last visit with ESL monotherapy versus adjunctive therapy (responder: 93.2% versus 70.4%; seizure freedom: 77.4% versus 25.9%). Overall incidence of AEs was similar in patients treated initially with ESL monotherapy and adjunctive therapy (29.4% versus 34.4%), and in patients treated at last visit with ESL monotherapy and adjunctive therapy (27.1% versus 30.8%).

Conclusion ESL was significantly more effective when used as monotherapy compared with adjunctive therapy; safety/tolerability was generally comparable.

Supported by Eisai

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