Efficacy and tolerability of levetiracetam as adjunctive therapy in Japanese patients with uncontrolled partial-onset seizures

被引:17
作者
Inoue, Yushi [1 ]
Yagi, Kazuichi [1 ,2 ]
Ikeda, Akio [3 ]
Sasagawa, Mutsuo [4 ]
Ishida, Shigenobu [5 ]
Suzuki, Atsushi [6 ]
Yoshida, Katsumi [6 ]
机构
[1] Shizuoka Inst Epilepsy & Neurol Disorders, NHO, Shizuoka 4208688, Japan
[2] Yaizu Hosp, Yaizu, Shizuoka, Japan
[3] Kyoto Univ, Sch Med, Dept Epilepsy Movement Disorders & Physiol, Kyoto 606, Japan
[4] Toyosato Hosp, Tsukuba, Ibaraki, Japan
[5] Akeno Med Clin, Ohita, Japan
[6] UCB Pharma, Tokyo, Japan
关键词
adjunctive therapy; antiepileptic drug; efficacy; levetiracetam; partial-onset seizures; PLACEBO-CONTROLLED TRIAL; REFRACTORY PARTIAL SEIZURES; MULTICENTER DOUBLE-BLIND; ADD-ON THERAPY; 2000; MG/DAY; BINDING; PROTEIN; SAFETY; SV2A;
D O I
10.1111/pcn.12300
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
AimsThe aim of this study was to confirm the efficacy and safety of adjunctive levetiracetam in adult Japanese patients with uncontrolled partial-onset seizures. MethodsIn a double-blind, placebo-controlled, confirmatory trial, eligible patients were randomized to receive levetiracetam 500, 1000, 2000, or 3000mg/day or placebo for 16 weeks. The primary end-point was percentage reduction from baseline in seizure frequency/week over a 12-week evaluation period. Tolerability assessments were also conducted. Findings of this and a previous randomized, double-blind trial were compared. ResultsOf 401 patients screened, 352 were randomized and 316 completed the study. Median percentage reduction in seizure frequency/week from baseline was 12.92%, 18.00%, 11.11% and 31.67% in the levetiracetam 500, 1000, 2000 and 3000-mg groups, respectively, compared with 12.50% in the placebo group. Unlike the previous trial, the primary efficacy analysis between the levetiracetam 1000 and 3000-mg and placebo groups did not reach statistical significance (P=0.067). Exploratory analyses demonstrated that the difference in seizure reduction versus placebo was 14.93% (95% confidence interval, 1.98-27.64; P=0.025) for the levetiracetam 3000-mg group. All levetiracetam doses were well tolerated. The main difference between the two trials was a high placebo response in the present trial. ConclusionsThe primary efficacy analysis did not reach statistical significance, a finding that could be attributed to an unexpectedly high placebo response. Nonetheless, exploratory analysis suggests that levetiracetam at 3000mg/day may, at least marginally, be beneficial for patients with uncontrolled partial-onset seizures.
引用
收藏
页码:640 / 648
页数:9
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