Literature DB >> 28927712

Real-world data on rufinamide treatment in patients with Lennox-Gastaut syndrome: Results from a European noninterventional registry study.

Marina Nikanorova1, Christian Brandt2, Stéphane Auvin3, Rob McMurray4.   

Abstract

INTRODUCTION: Rufinamide is approved for the adjunctive treatment of seizures associated with Lennox-Gastaut syndrome (LGS) in patients aged ≥4years. The objective of this study was to provide real-world, long-term data on patients with LGS initiating rufinamide as add-on therapy and patients with LGS receiving other antiepileptic drugs (AEDs).
METHODS: A Phase IV, noninterventional, multicenter registry study was conducted in patients with LGS aged ≥4years requiring modification to any AED treatment, including initiation of add-on rufinamide therapy. Safety/tolerability was assessed by evaluating treatment-emergent adverse events (TEAEs), and efficacy was assessed using a generic seizure frequency scale.
RESULTS: A total of 111 patients from 64 sites in 8 European countries were included, of whom 64 initiated rufinamide ("rufinamide" group) and 21 did not receive rufinamide at any time during the study ("no-rufinamide" group). Mean ages were 16.1years (rufinamide) and 15.0years (no rufinamide). The median duration of follow-up was >2years (range: 1.3-46.4months). Antiepileptic drug-related TEAEs were reported for 40.6% (rufinamide) and 33.3% (no rufinamide) of patients and led to discontinuation of 7.8% and 4.8%, respectively. The most frequently reported rufinamide-related TEAEs (≥5% patients) were somnolence (7.8%) and decreased appetite (6.3%). There were no unexpected safety/tolerability findings. At month 12, the proportion of patients with improvement in all seizures ("much improved" or "very much improved") was 28.6% (12/42) for the rufinamide group and 14.3% (2/14) for the no-rufinamide group.
CONCLUSION: The study provided valuable information on LGS and its management, and evidence that rufinamide has a consistent and generally favorable safety/tolerability profile when used in routine clinical practice. CLINICALTRIALS. GOV IDENTIFIER: NCT01991041.
Copyright © 2017 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Antiepileptic drug; Epilepsy; Lennox–Gastaut syndrome; Real-world; Registry; Rufinamide

Mesh:

Substances:

Year:  2017        PMID: 28927712     DOI: 10.1016/j.yebeh.2017.08.026

Source DB:  PubMed          Journal:  Epilepsy Behav        ISSN: 1525-5050            Impact factor:   2.937


  4 in total

Review 1.  Elucidating the Potential Side Effects of Current Anti-Seizure Drugs for Epilepsy.

Authors:  Enes Akyüz; Betül Köklü; Cansu Ozenen; Alina Arulsamy; Mohd Farooq Shaikh
Journal:  Curr Neuropharmacol       Date:  2021       Impact factor: 7.708

Review 2.  Adjunctive Rufinamide in Children with Lennox-Gastaut Syndrome: A Literature Review.

Authors:  Ganna Balagura; Antonella Riva; Francesca Marchese; Alberto Verrotti; Pasquale Striano
Journal:  Neuropsychiatr Dis Treat       Date:  2020-02-05       Impact factor: 2.570

Review 3.  Expanding the Treatment Landscape for Lennox-Gastaut Syndrome: Current and Future Strategies.

Authors:  Adam Strzelczyk; Susanne Schubert-Bast
Journal:  CNS Drugs       Date:  2021-01-21       Impact factor: 5.749

Review 4.  Psychobehavioural and Cognitive Adverse Events of Anti-Seizure Medications for the Treatment of Developmental and Epileptic Encephalopathies.

Authors:  Adam Strzelczyk; Susanne Schubert-Bast
Journal:  CNS Drugs       Date:  2022-10-04       Impact factor: 6.497

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.