Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox-Gastaut syndrome: Interim analysis of an open-label extension study.

Renzo Guerrini, Ronald Davis, Shikha Polega, Arnold R Gammaitoni, Bradley S Galer, Gail M Farfel, Michael Lock, Anupam Agarwal, Rima Nabbout, Sameer M Zuberi, Kate Riney, Lieven Lagae, Katherine C Nickels, Joseph Sullivan, Berten Ceulemans, Ingrid E Scheffer, Kelly G Knupp, David Dai, Antonio Gil-Nagel

Journal: Epilepsia 2023;64(1):139-151

PMID: 36196777

Abstract

OBJECTIVE

This study was undertaken to evaluate the long-term safety and effectiveness of fenfluramine in patients with Lennox-Gastaut syndrome (LGS).

METHODS

Eligible patients with LGS who completed a 14-week phase 3 randomized clinical trial enrolled in an open-label extension (OLE; NCT03355209). All patients were initially started on .2 mg/kg/day fenfluramine and after 1 month were titrated by effectiveness and tolerability, which were assessed at 3-month intervals. The protocol-specified treatment duration was 12 months, but COVID-19-related delays resulted in 142 patients completing their final visit after 12 months.

RESULTS

As of October 19, 2020, 247 patients were enrolled in the OLE. Mean age was 14.3 ± 7.6 years (79 [32%] adults) and median fenfluramine treatment duration was 364 days; 88.3% of patients received 2-4 concomitant antiseizure medications. Median percentage change in monthly drop seizure frequency was -28.6% over the entire OLE (n = 241) and -50.5% at Month 15 (n = 142, p < .0001); 75 of 241 patients (31.1%) experienced ≥50% reduction in drop seizure frequency. Median percentage change in nondrop seizure frequency was -45.9% (n = 192, p = .0038). Generalized tonic-clonic seizures (GTCS) and tonic seizures were most responsive to treatment, with median reductions over the entire OLE of 48.8% (p < .0001, n = 106) and 35.8% (p < .0001, n = 186), respectively. A total of 37.6% (95% confidence interval [CI] = 31.4%-44.1%, n = 237) of investigators and 35.2% of caregivers (95% CI = 29.1%-41.8%, n = 230) rated patients as Much Improved/Very Much Improved on the Clinical Global Impression of Improvement scale. The most frequent treatment-emergent adverse events were decreased appetite (16.2%) and fatigue (13.4%). No cases of valvular heart disease (VHD) or pulmonary arterial hypertension (PAH) were observed.

SIGNIFICANCE

Patients with LGS experienced sustained reductions in drop seizure frequency on fenfluramine treatment, with a particularly robust reduction in frequency of GTCS, the key risk factor for sudden unexpected death in epilepsy. Fenfluramine was generally well tolerated; VHD or PAH was not observed long-term. Fenfluramine may provide an important long-term treatment option for LGS.

© 2022 UCB and The Authors. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.

Address: University of Colorado, Children's Hospital Colorado, Aurora, Colorado, USA.; University of Melbourne, Austin Hospital and Royal Children's Hospital, Melbourne, Victoria, Australia.; Department of Pediatric Neurology, Antwerp University Hospital, Antwerp, Belgium.; University of California, San Francisco Weill Institute for Neurosciences, Benioff Children's Hospital, San Francisco, California, USA.; Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.; Member of the European Reference Network EpiCARE, Department of Pediatric Neurology, University of Leuven, Leuven, Belgium.; Pediatric Neurology and Neurogenetics Unit, Anna Meyer Children's Hospital, University of Florence, Florence, Italy.; Stella Maris Foundation, Scientific Institute for Research and Health Care, Pisa, Italy.; Paediatric Neurosciences Research Group, Royal Hospital for Children, Glasgow, UK.; Reference Center for Rare Epilepsies, Necker-Sick Children University Hospital, Public Hospital Network of Paris, member of EpiCARE, Imagine Institute, Paris Cité University, Paris, France.; Neuroscience Unit, Queensland Children's Hospital, South Brisbane, Queensland, Australia.; School of Clinical Medicine, University of Queensland, St Lucia, Queensland, Australia.; Zogenix (now a part of UCB), Emeryville, California, USA.; Independent Consultant, Zogenix (now a part of UCB), Haiku, Hawaii, USA.; Syneos Health, Morrisville, North Carolina, USA.; Neurology and Epilepsy Research Center, Orlando, Florida, USA.; Ruber International Hospital, Madrid, Spain.
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