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Title: | Fenfluramine provides clinically meaningful reduction in frequency of drop seizures in patients with Lennox-Gastaut syndrome: interim analysis of an open-label extension study. | Austin Authors: | Knupp, Kelly G;Scheffer, Ingrid E ;Ceulemans, Berten;Sullivan, Joseph;Nickels, Katherine C;Lagae, Lieven;Guerrini, Renzo;Zuberi, Sameer M;Nabbout, Rima;Riney, Kate;Agarwal, Anupam;Lock, Michael;Dai, David;Farfel, Gail M;Galer, Bradley S;Gammaitoni, Arnold R;Polega, Shikha;Davis, Ronald;Gil-Nagel, Antonio | Affiliation: | University of Colorado, Children's Hospital Colorado, Aurora, CO, USA. School of Clinical Medicine, University of Queensland, St Lucia, QLD, Australia Neuroscience Unit, Queensland Children's Hospital, South Brisbane, QLD, Australia Austin Health Department of Paediatric Neurology, Antwerp University Hospital, Antwerp, Belgium. University of California San Francisco Weill Institute for Neurosciences, Benioff Children's Hospital, San Francisco, CA, USA.. Mayo Clinic, Department of Neurology, Rochester, MN, USA. Member of the European Reference Network EpiCARE; Department of Paediatric Neurology, University of Leuven, Leuven, Belgium.. Pediatric Neurology and Neurogenetics Unit, Anna Meyer Children's Hospital, University of Florence, Florence, Italy; IRCCS Fondazione Stella Maris, Pisa, Italy.. Paediatric Neurosciences Research Group, Royal Hospital for Children, Glasgow, United Kingdom.. Reference Centre for Rare Epilepsies, Hôpital Universitaire Necker-Enfants Malades, APHP, Member of EPICARE, Institut Imagine, Université Paris Cité, Paris, France.. Formerly Zogenix, Inc. (now a part of UCB), Emeryville, CA, USA.. Independent consultant, Zogenix, Inc. (now a part of UCB); Haiku, HI, USA.. Syneos Health, Morrisville, NC, USA.. Formerly Zogenix, Inc. (now a part of UCB), Emeryville, CA, USA.. Zogenix, Inc. (now a part of UCB), Emeryville, CA, USA.. Neurology and Epilepsy Research Center, Orlando, FL, USA.. Hospital Ruber Internacional, Madrid, Spain.. |
Issue Date: | 2023 | Date: | 2022 | Publication information: | Epilepsia 2023; 64(1) | Abstract: | To evaluate the long-term safety and effectiveness of fenfluramine in patients with Lennox-Gastaut syndrome (LGS). 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 0.2 mg/kg/day fenfluramine and, after 1 month, were titrated to 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. As of 10/19/2020, 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<0.0001); 75/241 patients (31.1%) experienced ≥50% reduction in drop seizure frequency. Median percentage change in non-drop seizure frequency was -45.9% (n=192; P=0.0038). Generalized tonic-clonic seizures (GTCS) and tonic seizures were most responsive to treatment, with median reductions over the entire OLE of 48.8% (P<0.0001; n=106) and 35.8% (P<0.0001; n=186), respectively. A total of 37.6% (95% 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 (CGI-I) 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. 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 SUDEP. Fenfluramine was generally well tolerated; VHD or PAH was not observed long-term. Fenfluramine may provide an important long-term treatment option for LGS. | URI: | https://ahro.austin.org.au/austinjspui/handle/1/31005 | DOI: | 10.1111/epi.17431 | ORCID: | https://orcid.org/0000-0002-1967-0827 https://orcid.org/0000-0002-2311-2174 https://orcid.org/0000-0002-6579-3035 https://orcid.org/0000-0002-7118-0139 https://orcid.org/0000-0002-7272-7079 https://orcid.org/0000-0001-5877-4074 https://orcid.org/0000-0002-1122-3555 https://orcid.org/0000-0002-4735-3327 https://orcid.org/0000-0002-4775-2862 |
Journal: | Epilepsia | PubMed URL: | 36196777 | Type: | Journal Article | Subjects: | Lennox-Gastaut syndrome developmental and epileptic encephalopathies fenfluramine long-term open-label extension |
Appears in Collections: | Journal articles |
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