Slow Titration of Cannabidiol Add-On in Drug-Resistant Epilepsies Can Improve Safety With Maintained Efficacy in an Open-Label Study

被引:30
|
作者
D'Onofrio, Gianluca [1 ,2 ]
Kuchenbuch, Mathieu [1 ,3 ]
Hachon-Le Camus, Caroline [4 ]
Desnous, Beatrice [5 ]
Staath, Veronique [6 ]
Napuri, Sylvia [7 ]
Ville, Dorothee [8 ]
Pedespan, Jean-Michel [9 ]
Lepine, Anne [5 ]
Cances, Claude [4 ]
de Saint-Martin, Anne [6 ]
Teng, Theo [1 ]
Chemaly, Nicole [1 ,3 ]
Milh, Mathieu [5 ]
Villeneuve, Nathalie [5 ]
Nabbout, Rima [1 ,3 ]
机构
[1] Hop Necker Enfants Malad, AP HP, Reference Ctr Rare Epilepsies, Dept Pediat Neurol, Paris, France
[2] Univ Padua, Dept Women & Child Hlth, Pediat Residency, Padua, Italy
[3] Univ Paris, Imagine Inst, Lab Translat Res Neurol Disorders, INSERM UMR 1163, Paris, France
[4] Toulouse Univ Hosp, Dept Pediat Neurol, Hop Enfants, Toulouse, France
[5] Timone Children Hosp, AP HM, Pediat Neurol Dept, Marseille, France
[6] Strasbourg Univ Hosp, Hop Hautepierre, Dept Pediat Neurol, Strasbourg, France
[7] Univ Rennes, Rennes Univ Hosp, Dept Pediat, Rennes, France
[8] CNRS UMR 5304, Dept Pediat Neurol, Bron, France
[9] Pellegrin Univ Hosp, Dept Pediat, Bordeaux, France
来源
FRONTIERS IN NEUROLOGY | 2020年 / 11卷
关键词
Dravet; Lennox-Gastaut; adverse events; liver function; tolerability; drug resistant; SEIZURES; TRIALS;
D O I
10.3389/fneur.2020.00829
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective:To assess adverse events (AEs) and efficacy of add-on cannabidiol (CBD) with a slower titration protocol in pediatric clinical practice. Methods:We conducted a prospective, open-label, multicenter study in seven French reference centers for rare epilepsies. Patients had slow titration to reach a target dose of 10 mg/kg/day within at least 1 month and then gradually increased to a maximum dose of 20 mg/kg/day. We analyzed AEs and efficacy at M1 (month 1), M2, and M6, comparing two sets of subgroups: Dravet syndrome (DS) vs. Lennox-Gastaut (LGS) and patients with clobazam (CLB+) vs. patients without (CLB-). Results:One hundred and twenty-five patients were enrolled (62 LGS, 48 DS, 5 Tuberous sclerosis, and 10 other etiologies). Median concomitant antiepileptic drugs (AEDs) was three (25th percentile: 3, 75th percentile: 4). Patients received a dose of 10 (10-12), 14 (10-20), and 15.5 mg/kg/day (10-20) at M1, M2, and M6, respectively. Twenty-six patients discontinued CBD, 19 due to lack of efficacy, 2 due to AEs, 4 for both, and 1 had a sudden unexpected death in epilepsy. AEs were reported in 61 patients (48.8%), mainly somnolence (n= 26), asthenia (n= 20), and behavior disorders (n= 16). Abnormal transaminases (>= 3 times) were reported in 11 patients receiving both valproate and clobazam. AEs were significantly higher at M2 (p= 0.03) and increased with the number of AEDs (p= 0.03). At M6, total seizure frequency change from baseline was -41% +/- 37.5% (mean +/- standard deviation), and 28 patients (37.8%) had a reduction >= 50%. AE and efficacy did not differ between DS vs. LGS and CLB+ vs. CLB- patients. Significance:A slower titration of CBD dose delivered better tolerance with comparable efficacy to previous trials. Concomitant CLB did not increase efficacy rates but in a few cases increased AEs. This slow titration scheme should help guide clinicians prescribing CBD and allow patients to benefit from its potential efficacy.
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页数:11
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