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Published in: CNS Drugs 10/2020

01-10-2020 | Antiepileptic Drugs | Current Opinion

Fenfluramine for the Treatment of Dravet Syndrome and Lennox–Gastaut Syndrome

Authors: Ganna Balagura, Marta Cacciatore, Eleonora A. Grasso, Pasquale Striano, Alberto Verrotti

Published in: CNS Drugs | Issue 10/2020

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Abstract

The last 50 years has seen the introduction of a great number of antiepileptic drugs, relieving the burden of seizures for many patients. However, some conditions remain a challenge for epileptologists, especially Dravet syndrome and Lennox–Gastaut syndrome, which are severe epileptic and developmental encephalopathies characterized by multiple seizure types and electroencephalographic abnormalities that are often unresponsive to combinations of antiepileptic drugs. The re-purposing of an old drug such as fenfluramine could provide an indispensable tool for clinicians, especially because only a few drugs have been tested in relatively homogeneous populations, like Dravet syndrome. It could also provide insights into precision medicine approaches to the treatment of epileptic syndromes. We searched for relevant papers within MEDLINE, EMBASE, and the Clinical Trial Database, considering publications through July 2020. Pre-clinical studies show a mechanism of action for fenfluramine that goes beyond its pro-serotoninergic activity and that is at the intersection of several pathways involved in excitation/inhibition balance. From the ongoing clinical trial data, it is evident that fenfluramine is proving to be a promising antiepileptic drug with very favorable pharmacokinetics and with a good overall safety profile when used at a lower dosage (0.2–0.7 mg/kg/day), despite its previously link to major cardiac adverse events that prompted its withdrawal from the market in 1997. Here, we review the experimental and clinical evidence of the efficacy of fenfluramine, including the latest results from ongoing clinical trials, and critically discuss the future potential of fenfluramine in terms of safety and precision medicine. Available data from the literature suggest a very good efficacy for both epileptic syndromes with a reduction in seizure burden and a longer seizure-free interval. We note the higher prevalence of evidence in patients with Dravet syndrome. Fenfluramine has been used in association with both first- and second-line medications, while its use in monotherapy still needs to be assessed.
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Metadata
Title
Fenfluramine for the Treatment of Dravet Syndrome and Lennox–Gastaut Syndrome
Authors
Ganna Balagura
Marta Cacciatore
Eleonora A. Grasso
Pasquale Striano
Alberto Verrotti
Publication date
01-10-2020
Publisher
Springer International Publishing
Published in
CNS Drugs / Issue 10/2020
Print ISSN: 1172-7047
Electronic ISSN: 1179-1934
DOI
https://doi.org/10.1007/s40263-020-00755-z

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