Skip to main content
Erschienen in: CNS Drugs 10/2020

01.10.2020 | Current Opinion

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

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

Erschienen in: CNS Drugs | Ausgabe 10/2020

Einloggen, um Zugang zu erhalten

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.
Literatur
1.
Zurück zum Zitat Verrotti A, Striano P, Iapadre G, et al. The pharmacological management of Lennox-Gastaut syndrome and critical literature review. Seizure. 2018;63:17–25.CrossRef Verrotti A, Striano P, Iapadre G, et al. The pharmacological management of Lennox-Gastaut syndrome and critical literature review. Seizure. 2018;63:17–25.CrossRef
2.
Zurück zum Zitat Brigo F, Striano P, Balagura G, Belcastro V. Emerging drugs for the treatment of Dravet syndrome. Expert Opin Emerg Drugs. 2018;23(4):261–9.CrossRef Brigo F, Striano P, Balagura G, Belcastro V. Emerging drugs for the treatment of Dravet syndrome. Expert Opin Emerg Drugs. 2018;23(4):261–9.CrossRef
3.
Zurück zum Zitat Striano P, Verrotti A. Pharmacokinetics and drug interaction of antiepileptic drugs in children and adolescents. Paediatr Drugs. 2018;20:429–53.CrossRef Striano P, Verrotti A. Pharmacokinetics and drug interaction of antiepileptic drugs in children and adolescents. Paediatr Drugs. 2018;20:429–53.CrossRef
4.
Zurück zum Zitat Wurtman R, Wurtman J. Fenfluramine: back from the dead. Clin Ther. 2018;40:1420–2.CrossRef Wurtman R, Wurtman J. Fenfluramine: back from the dead. Clin Ther. 2018;40:1420–2.CrossRef
5.
Zurück zum Zitat Fuller R, Snoddy H, Robertson D. Mechanisms of effects of D-fenfluramine on brain serotonin metabolism in rats: uptake inhibition versus release. Pharmacol Biochem Behav. 1988;30:715–21.CrossRef Fuller R, Snoddy H, Robertson D. Mechanisms of effects of D-fenfluramine on brain serotonin metabolism in rats: uptake inhibition versus release. Pharmacol Biochem Behav. 1988;30:715–21.CrossRef
6.
Zurück zum Zitat Spedding M, Ouvry C, Millan M, et al. Neural control of dieting. Nature. 1996;380:488.CrossRef Spedding M, Ouvry C, Millan M, et al. Neural control of dieting. Nature. 1996;380:488.CrossRef
7.
Zurück zum Zitat Bonnycastle D, Giarman N, Paasonen M. Anticonvulsant compounds and 5-hydroxytryptamine in rat brain. Br J Pharmacol Chemother. 1957;12:228–31.CrossRef Bonnycastle D, Giarman N, Paasonen M. Anticonvulsant compounds and 5-hydroxytryptamine in rat brain. Br J Pharmacol Chemother. 1957;12:228–31.CrossRef
8.
Zurück zum Zitat Favale E, Rubino V, Mainardi P, Lunardi G, Albano C. Anticonvulsant effect of fluoxetine in humans. Neurology. 1995;45:1926–7.CrossRef Favale E, Rubino V, Mainardi P, Lunardi G, Albano C. Anticonvulsant effect of fluoxetine in humans. Neurology. 1995;45:1926–7.CrossRef
9.
Zurück zum Zitat Jobe P, Browning R. The serotonergic and noradrenergic effects of antidepressant drugs are anticonvulsant, not proconvulsant. Epilepsy Behav. 2005;7:602–19.CrossRef Jobe P, Browning R. The serotonergic and noradrenergic effects of antidepressant drugs are anticonvulsant, not proconvulsant. Epilepsy Behav. 2005;7:602–19.CrossRef
10.
Zurück zum Zitat Sourbron J, Smolders I, de Witte P, Lagae L. Pharmacological analysis of the anti-epileptic mechanisms of fenfluramine in scn1a mutant zebrafish. Front Pharmacol. 2017;8:191.CrossRef Sourbron J, Smolders I, de Witte P, Lagae L. Pharmacological analysis of the anti-epileptic mechanisms of fenfluramine in scn1a mutant zebrafish. Front Pharmacol. 2017;8:191.CrossRef
11.
Zurück zum Zitat Rodríguez-Muñoz M, Sánchez-Blázquez P, Garzón J. Fenfluramine diminishes NMDA receptor-mediated seizures via its mixed activity at serotonin 5HT2A and type 1 sigma receptors. Oncotarget. 2018;9:23373–89.CrossRef Rodríguez-Muñoz M, Sánchez-Blázquez P, Garzón J. Fenfluramine diminishes NMDA receptor-mediated seizures via its mixed activity at serotonin 5HT2A and type 1 sigma receptors. Oncotarget. 2018;9:23373–89.CrossRef
12.
Zurück zum Zitat Martin P, de Witte PAM, Maurice T, Gammaitoni A, Farfel G, Galer B. Fenfluramine acts as a positive modulator of sigma-1 receptors. Epilepsy Behav. 2020;105:106989.CrossRef Martin P, de Witte PAM, Maurice T, Gammaitoni A, Farfel G, Galer B. Fenfluramine acts as a positive modulator of sigma-1 receptors. Epilepsy Behav. 2020;105:106989.CrossRef
13.
Zurück zum Zitat Ceulemans B, Boel M, Leyssens K, Van Rossem C, Neels P, Jorens PG, et al. Successful use of fenfluramine as an add-on treatment for Dravet syndrome. Epilepsia. 2012;53:1131–9.CrossRef Ceulemans B, Boel M, Leyssens K, Van Rossem C, Neels P, Jorens PG, et al. Successful use of fenfluramine as an add-on treatment for Dravet syndrome. Epilepsia. 2012;53:1131–9.CrossRef
14.
Zurück zum Zitat Boyd B, Smith S, Gammaitoni A, Galer BS, Farfel GM. A phase I, randomized, open-label, single-dose, 3-period crossover study to evaluate the drug-drug interaction between ZX008 (fenfluramine HCl oral solution) and a regimen of stiripentol, clobazam, and valproate in healthy subjects. Int J Clin Pharmacol Ther. 2019;57:11–9.CrossRef Boyd B, Smith S, Gammaitoni A, Galer BS, Farfel GM. A phase I, randomized, open-label, single-dose, 3-period crossover study to evaluate the drug-drug interaction between ZX008 (fenfluramine HCl oral solution) and a regimen of stiripentol, clobazam, and valproate in healthy subjects. Int J Clin Pharmacol Ther. 2019;57:11–9.CrossRef
15.
Zurück zum Zitat Schoonjans A, Paelinck BP, Marchau F, et al. Low-dose fenfluramine significantly reduces seizure frequency in Dravet syndrome: a prospective study of a new cohort of patients. Eur J Neurol. 2017;24:309–14.CrossRef Schoonjans A, Paelinck BP, Marchau F, et al. Low-dose fenfluramine significantly reduces seizure frequency in Dravet syndrome: a prospective study of a new cohort of patients. Eur J Neurol. 2017;24:309–14.CrossRef
16.
Zurück zum Zitat Onakpoya IJ, Heneghan CJ, Aronson JK. Worldwide withdrawal of medicinal products because of adverse drug reactions: a systematic review and analysis. Crit Rev Toxicol. 2016;46:477–89.CrossRef Onakpoya IJ, Heneghan CJ, Aronson JK. Worldwide withdrawal of medicinal products because of adverse drug reactions: a systematic review and analysis. Crit Rev Toxicol. 2016;46:477–89.CrossRef
17.
Zurück zum Zitat Schoonjans A-S, Lagae L, Ceulemans B. Low-dose fenfluramine in the treatment of neurologic disorders: experience in Dravet syndrome. Ther Adv Neurol Disord. 2015;8:328–38.CrossRef Schoonjans A-S, Lagae L, Ceulemans B. Low-dose fenfluramine in the treatment of neurologic disorders: experience in Dravet syndrome. Ther Adv Neurol Disord. 2015;8:328–38.CrossRef
18.
Zurück zum Zitat Humbert M, Deng Z, Simonneau G, et al. BMPR2 germline mutations in pulmonary hypertension associated with fenfluramine derivatives. Eur Respir J. 2002;20:518–23.CrossRef Humbert M, Deng Z, Simonneau G, et al. BMPR2 germline mutations in pulmonary hypertension associated with fenfluramine derivatives. Eur Respir J. 2002;20:518–23.CrossRef
19.
Zurück zum Zitat Schoonjans AS, Marchau F, Paelinck BP, et al. Cardiovascular safety of low-dose fenfluramine in Dravet syndrome: a review of its benefit-risk profile in a new patient population. Curr Med Res Opin. 2017;33:1773–81.CrossRef Schoonjans AS, Marchau F, Paelinck BP, et al. Cardiovascular safety of low-dose fenfluramine in Dravet syndrome: a review of its benefit-risk profile in a new patient population. Curr Med Res Opin. 2017;33:1773–81.CrossRef
20.
Zurück zum Zitat Lagae L, Sullivan J, Knupp K, Laux L, Polster T, Nikanorova M, et al. Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial. Lancet. 2020;394:2243–54.CrossRef Lagae L, Sullivan J, Knupp K, Laux L, Polster T, Nikanorova M, et al. Fenfluramine hydrochloride for the treatment of seizures in Dravet syndrome: a randomised, double-blind, placebo-controlled trial. Lancet. 2020;394:2243–54.CrossRef
21.
Zurück zum Zitat Dinday, Baraban SC. Large-scale phenotype-based antiepileptic drug screening in a zebrafish model of Dravet syndrome. eNeuro. 2015;2:ENEURO.0068-15.2015.CrossRef Dinday, Baraban SC. Large-scale phenotype-based antiepileptic drug screening in a zebrafish model of Dravet syndrome. eNeuro. 2015;2:ENEURO.0068-15.2015.CrossRef
22.
Zurück zum Zitat Zhang Y, Kecskés A, Copmans D, Langlois M, Crawford AD, Ceulemans B, et al. Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: inhibition of epileptic seizures by the serotonin agonist fenfluramine. PLoS ONE. 2015;10:e0125898.CrossRef Zhang Y, Kecskés A, Copmans D, Langlois M, Crawford AD, Ceulemans B, et al. Pharmacological characterization of an antisense knockdown zebrafish model of Dravet syndrome: inhibition of epileptic seizures by the serotonin agonist fenfluramine. PLoS ONE. 2015;10:e0125898.CrossRef
25.
Zurück zum Zitat Lazarova M, Bendotti C, Samarin R. Studies on the role of serotonin in different regions of the rat central nervous system on pentylenetetrazol-induced seizures and the effect of Di-N-propylacetate. Naunyn Schmiedebergs Arch Pharmacol. 1983;322:147–52.CrossRef Lazarova M, Bendotti C, Samarin R. Studies on the role of serotonin in different regions of the rat central nervous system on pentylenetetrazol-induced seizures and the effect of Di-N-propylacetate. Naunyn Schmiedebergs Arch Pharmacol. 1983;322:147–52.CrossRef
26.
Zurück zum Zitat Silenieks LB, Carroll NK, Van Niekerk A, Van Niekerk E, Taylor C, Upton N, et al. Evaluation of selective 5-HT 2C agonists in acute seizure models. ACS Chem Neurosci. 2019;10:3284–95.CrossRef Silenieks LB, Carroll NK, Van Niekerk A, Van Niekerk E, Taylor C, Upton N, et al. Evaluation of selective 5-HT 2C agonists in acute seizure models. ACS Chem Neurosci. 2019;10:3284–95.CrossRef
28.
Zurück zum Zitat Tupal S, Faingold CL. Fenfluramine, a serotonin-releasing drug, prevents seizure-induced respiratory arrest and is anticonvulsant in the DBA/1 mouse model of SUDEP. Epilepsia. 2019;60:485–94.PubMed Tupal S, Faingold CL. Fenfluramine, a serotonin-releasing drug, prevents seizure-induced respiratory arrest and is anticonvulsant in the DBA/1 mouse model of SUDEP. Epilepsia. 2019;60:485–94.PubMed
29.
Zurück zum Zitat Boel M, Casaer P. Add-on therapy of fenfluramine in intractable self-induced epilepsy. Neuropediatrics. 1996;27:171–3.CrossRef Boel M, Casaer P. Add-on therapy of fenfluramine in intractable self-induced epilepsy. Neuropediatrics. 1996;27:171–3.CrossRef
30.
Zurück zum Zitat Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. Am J Hum Genet. 2001;68:1327–32.CrossRef Claes L, Del-Favero J, Ceulemans B, Lagae L, Van Broeckhoven C, De Jonghe P. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy. Am J Hum Genet. 2001;68:1327–32.CrossRef
32.
Zurück zum Zitat Knupp KG, Lagae L, Thiele EA et al. ZX008 (fenfluramine hydrochloride oral solution) provides clinically meaningful reductions in seizure frequency irrespective of concomitant AEDs commonly used in Dravet syndrome: pooled analysis of two phase 3 trials [poster no. 3.430]. Presented at the American Epilepsy Society (AES) Annual Meeting; 6–10 December, 2019; Baltimore (MD).* (Unpublished posters). Knupp KG, Lagae L, Thiele EA et al. ZX008 (fenfluramine hydrochloride oral solution) provides clinically meaningful reductions in seizure frequency irrespective of concomitant AEDs commonly used in Dravet syndrome: pooled analysis of two phase 3 trials [poster no. 3.430]. Presented at the American Epilepsy Society (AES) Annual Meeting; 6–10 December, 2019; Baltimore (MD).* (Unpublished posters).
33.
Zurück zum Zitat Sullivan J, Nabbout R, Knupp K, et al. ZX008 (fenfluramine HCl oral solution) provides long-term, clinically meaningful reduction of convulsive seizure frequency in young (< 6 years old) Dravet syndrome subjects: analysis from a long-term open-label study [poster]. In: Presented as part of the Zogenix Scientific Exhibit during the American Epilepsy Society (AES) Annual Meeting; 8 December, 2019; Baltimore (MD).* (Unpublished posters). Sullivan J, Nabbout R, Knupp K, et al. ZX008 (fenfluramine HCl oral solution) provides long-term, clinically meaningful reduction of convulsive seizure frequency in young (< 6 years old) Dravet syndrome subjects: analysis from a long-term open-label study [poster]. In: Presented as part of the Zogenix Scientific Exhibit during the American Epilepsy Society (AES) Annual Meeting; 8 December, 2019; Baltimore (MD).* (Unpublished posters).
34.
Zurück zum Zitat Bishop KI, Isquith PK, Gioia GA, et al. Profound reduction in seizure frequency (≥ 75%) leads to improved everyday executive function: analysis from a phase 3 study of ZX008 (fenfluramine HCl) in children/young adults with Dravet syndrome [poster no. 2.438]. In: Presented at American Epilepsy Society (AES) Annual Meeting; 6–10 December, 2019; Baltimore (MD).* (Unpublished posters). Bishop KI, Isquith PK, Gioia GA, et al. Profound reduction in seizure frequency (≥ 75%) leads to improved everyday executive function: analysis from a phase 3 study of ZX008 (fenfluramine HCl) in children/young adults with Dravet syndrome [poster no. 2.438]. In: Presented at American Epilepsy Society (AES) Annual Meeting; 6–10 December, 2019; Baltimore (MD).* (Unpublished posters).
36.
Zurück zum Zitat Lagae L, Schoonjans AS, Gammaitoni AR, Galer BS, Ceulemans B. A pilot, open-label study of the effectiveness and tolerability of low-dose ZX008 (fenfluramine HCl) in Lennox-Gastaut syndrome. Epilepsia. 2018;59:1881–8.CrossRef Lagae L, Schoonjans AS, Gammaitoni AR, Galer BS, Ceulemans B. A pilot, open-label study of the effectiveness and tolerability of low-dose ZX008 (fenfluramine HCl) in Lennox-Gastaut syndrome. Epilepsia. 2018;59:1881–8.CrossRef
Metadaten
Titel
Fenfluramine for the Treatment of Dravet Syndrome and Lennox–Gastaut Syndrome
verfasst von
Ganna Balagura
Marta Cacciatore
Eleonora A. Grasso
Pasquale Striano
Alberto Verrotti
Publikationsdatum
01.10.2020
Verlag
Springer International Publishing
Erschienen in
CNS Drugs / Ausgabe 10/2020
Print ISSN: 1172-7047
Elektronische ISSN: 1179-1934
DOI
https://doi.org/10.1007/s40263-020-00755-z

Weitere Artikel der Ausgabe 10/2020

CNS Drugs 10/2020 Zur Ausgabe

Leitlinien kompakt für die Neurologie

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Hirnblutung unter DOAK und VKA ähnlich bedrohlich

17.05.2024 Direkte orale Antikoagulanzien Nachrichten

Kommt es zu einer nichttraumatischen Hirnblutung, spielt es keine große Rolle, ob die Betroffenen zuvor direkt wirksame orale Antikoagulanzien oder Marcumar bekommen haben: Die Prognose ist ähnlich schlecht.

Was nützt die Kraniektomie bei schwerer tiefer Hirnblutung?

17.05.2024 Hirnblutung Nachrichten

Eine Studie zum Nutzen der druckentlastenden Kraniektomie nach schwerer tiefer supratentorieller Hirnblutung deutet einen Nutzen der Operation an. Für überlebende Patienten ist das dennoch nur eine bedingt gute Nachricht.

Thrombektomie auch bei großen Infarkten von Vorteil

16.05.2024 Ischämischer Schlaganfall Nachrichten

Auch ein sehr ausgedehnter ischämischer Schlaganfall scheint an sich kein Grund zu sein, von einer mechanischen Thrombektomie abzusehen. Dafür spricht die LASTE-Studie, an der Patienten und Patientinnen mit einem ASPECTS von maximal 5 beteiligt waren.

Schwindelursache: Massagepistole lässt Otholiten tanzen

14.05.2024 Benigner Lagerungsschwindel Nachrichten

Wenn jüngere Menschen über ständig rezidivierenden Lagerungsschwindel klagen, könnte eine Massagepistole der Auslöser sein. In JAMA Otolaryngology warnt ein Team vor der Anwendung hochpotenter Geräte im Bereich des Nackens.

Update Neurologie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.