Adjunctive levetiracetam in children, adolescents, and adults with primary generalized seizures: Open-label, noncomparative, multicenter, long-term follow-up study

被引:36
作者
Delanty, Norman [1 ]
Jones, John [2 ]
Tonner, Francoise [3 ]
机构
[1] Beaumont Hosp, Div Neurol, Epilepsy Programme, Dublin 9, Ireland
[2] UCB Pharma, Raleigh, NC USA
[3] UCB Pharma, Brussels, Belgium
关键词
Clinical trial; Antiepileptic drugs; Absence seizures; Myoclonic seizures; Tonic-clonic seizures; Idiopathic generalized epilepsy; PARTIAL-ONSET SEIZURES; PLACEBO-CONTROLLED TRIAL; ADD-ON THERAPY; DOUBLE-BLIND; MANAGEMENT ISSUES; EPILEPSY; LAMOTRIGINE; EXPOSURE; EFFICACY; PROTEIN;
D O I
10.1111/j.1528-1167.2011.03300.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose: To evaluate the long-term efficacy and tolerability of adjunctive levetiracetam (LEV) in patients with uncontrolled idiopathic generalized epilepsy (IGE). Methods: This phase III, open-label, long-term, follow-up study (N167; NCT00150748) enrolled patients (4 to < 65 years) with primary generalized seizures (tonicclonic, myoclonic, absence). Patients received adjunctive LEV at individualized doses (1,000-4,000 mg/day; 20-80 mg/kg/day for children/adolescents weighing < 50 kg). Efficacy results are reported for all seizure types [ intention-to-treat (ITT) population, N = 217] and subpopulations with tonic-clonic (n = 152), myoclonic (n = 121), and/or absence (n = 70) seizures at baseline. Key Findings: One hundred twenty-five (57.6%) of 217 patients were still receiving treatment at the end of the study. Mean (standard deviation, SD) LEV dose was 2,917.5 (562.9) mg/day. Median (Q1-Q3) exposure to LEV was 2.1 (1.5-2.8) years, and the maximum duration was 4.6 years. Most patients were taking one (124/217, 57.1%) or 2 (92/217, 42.4%) concomitant antiepileptic drugs (AEDs). Seizure freedom of 6 months (all seizure types; primary efficacy end point) was achieved by 122 (56.2%) of 217 patients, and 49 (22.6%) of 217 patients had complete seizure freedom. Seizure freedom of 6 months from tonic-clonic, myoclonic, and absence seizures was achieved by 95 (62.5%) of 152, 75 (62.0%) of 121, and 44 (62.9%) of 70 patients, respectively. Mean (SD) maximum seizure freedom duration was 371.7 (352.4) days. At least one treatment-emergent adverse event (TEAE) was reported by 165 (76%) of 217 patients; most TEAEs were mild/moderate in severity, with no indication of an increased incidence over time. Seventeen (7.8%) of 217 patients discontinued medication because of TEAEs. The most common psychiatric TEAEs were depression (16/217, 7.4%), insomnia (9/217, 4.1%), nervousness (8/ 217, 3.7%), and anxiety (7/217, 3.2%). Significance: Adjunctive LEV (range 1,000-4,000 mg/day) demonstrated efficacy as a long-term treatment for primary generalized seizures in children, adolescents, and adults with IGE, and was well tolerated.
引用
收藏
页码:111 / 119
页数:9
相关论文
共 46 条
[1]   Long-term efficacy of levetiracetam for partial seizures [J].
Abou-Khalil, B ;
Schaich, L .
SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2005, 14 (08) :577-585
[2]  
Alekar S, 2009, EPILEPSIA, V50, P245
[3]   PROPOSAL FOR REVISED CLASSIFICATION OF EPILEPSIES AND EPILEPTIC SYNDROMES [J].
不详 .
EPILEPSIA, 1989, 30 (04) :389-399
[4]  
[Anonymous], 2010, Survival Analysis Using SAS: A Practical Guide
[5]   Antiepileptic drug use of women with epilepsy and congenital malformations in offspring [J].
Artama, M ;
Auvinen, A ;
Raudaskoski, T ;
Isojärvi, I ;
Isojärvi, J .
NEUROLOGY, 2005, 64 (11) :1874-1878
[6]   Levetiracetam:: a long-term follow-up study of efficacy and safety [J].
Bauer, J. ;
Ben-Menachem, E. ;
Kraemer, G. ;
Fryze, W. ;
Da Silva, S. ;
Kasteleijn-Nolst Trenite, D. G. A. .
ACTA NEUROLOGICA SCANDINAVICA, 2006, 114 (03) :169-176
[7]   Efficacy and tolerability of levetiracetam 3000 mg/d in patients with refractory partial seizures: A multicenter, double-blind, responder-selected study evaluating monotherapy [J].
Ben-Menachem, E ;
Falter, T .
EPILEPSIA, 2000, 41 (10) :1276-1283
[8]   Practical management issues for idiopathic generalized epilepsies [J].
Benbadis, SR .
EPILEPSIA, 2005, 46 :125-132
[9]   Idiopathic generalized epilepsy and choice of antiepileptic drugs [J].
Benbadis, SR ;
Tatum, WO ;
Gieron, M .
NEUROLOGY, 2003, 61 (12) :1793-1795
[10]   Placebo-controlled study of levetiracetam in idiopathic generalized epilepsy [J].
Berkovic, S. F. ;
Knowlton, R. C. ;
Leroy, R. F. ;
Schiemann, J. ;
Falter, U. .
NEUROLOGY, 2007, 69 (18) :1751-1760