Stiripentol in childhood partial epilepsy: Randomized placebo-controlled trial with enrichment and withdrawal design

被引:43
作者
Chiron, Catherine
Tonnelier, Sylvie
Rey, Elisabeth
Brunet, Marie-Lucie
Tran, Agner
d'Athis, Philippe
Vincent, Jean
Dulac, Olivier
Pons, Gerard
机构
[1] Hop Necker Enfants Malad, INSERM, U663, Serv Neurol & Metab, F-75015 Paris, France
[2] Hop Necker Enfants Malad, Neuropediat Dept, F-75015 Paris, France
[3] Univ Paris 05, F-75015 Paris, France
[4] Hop St Vincent de Paul, Dept Perinatal & Pediat Pharmacol, F-75674 Paris, France
[5] Biocodex, Dept Pharm, Montrouge, France
关键词
D O I
10.1177/08830738060210062101
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Stiripentol, a new antiepileptic drug inhibiting cytochrome P450-enzymes, suggested some efficacy when combined with carbamazepine in an open trial in refractory partial epilepsy of childhood. Our objective was to test these results in a placebo-controlled trial. To limit the number of patients included, we used an enrichment and withdrawal design. Among the 67 children entered in a 4-month open add-on stiripentol study following a 1-month single-blind placebo baseline, the 32 responders were randomized for 2 months either to continue stiripentol (n = 17) or to withdraw to placebo (n = 15). If seizures increased by at least 50% after randomization compared with baseline, the patients dropped out (primary end point): there were six patients on stiripentol and eight patients on placebo (not significant). However, a decrease in seizure frequency compared with baseline (secondary end point) was greater on stiripentol (-75%) than on placebo (-22%) (P <.025). Twelve patients experienced at least one adverse event on stiripentol (71%) compared with four patients on placebo (27%); none were reported as severe. The combination of stiripentol and carbamazepine proved to reduce seizure frequency in children with refractory partial epilepsy, although it failed to show a significant impact according to the escape criteria selected as the primary end point in the present study, for ethical reasons.
引用
收藏
页码:496 / 502
页数:7
相关论文
共 15 条
[11]   Risk factors for status epilepticus in children with symptomatic epilepsy [J].
Novak, G ;
Maytal, J ;
Alshansky, A ;
Ascher, C .
NEUROLOGY, 1997, 49 (02) :533-537
[12]   Stiripentol: Efficacy and tolerability in children with epilepsy [J].
Perez, J ;
Chiron, C ;
Musial, C ;
Rey, E ;
Blehaut, H ;
d'Athis, JP ;
Vincent, J ;
Dulac, O .
EPILEPSIA, 1999, 40 (11) :1618-1626
[13]   A double-blind, randomized trial of topiramate in Lennox-Gastaut syndrome [J].
Sachdeo, RC ;
Glauser, TA ;
Ritter, F ;
Reife, R ;
Lim, P ;
Pledger, G .
NEUROLOGY, 1999, 52 (09) :1882-1887
[14]   Monotherapy comparative trials: placebos and suboptimal comparators [J].
Schwabe, S .
EPILEPSY RESEARCH, 2001, 45 (1-3) :93-96
[15]   Effect of stiripentol on carbamazepine plasma concentration and metabolism in epileptic children [J].
Tran, A ;
VauzelleKervroedan, F ;
Rey, E ;
Pons, G ;
dAthis, P ;
Chiron, C ;
Dulac, O ;
Renard, F ;
Olive, G .
EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY, 1996, 50 (06) :497-500