Flexible dosing of adjunctive zonisamide in the treatment of adult partial-onset seizures: a non-comparative, open-label study (ZEUS)

被引:21
作者
Dupont, S. [1 ]
Striano, S. [2 ]
Trinka, E. [3 ]
Springub, J. [4 ]
Giallonardo, A. T. [5 ]
Smith, P. [6 ]
Ellis, S. [7 ]
Yeates, A. [8 ]
Baker, G. [9 ]
机构
[1] UPMC, Unite Epilepsie, Neurol Clin, Hop La Pitie Salpetriere,APHP, Paris, France
[2] Univ Naples Federico II, Dept Neurol Sci, Naples, Italy
[3] Med Univ, Dept Neurol, Innsbruck, Austria
[4] Joint Practice Neurol & Psychiat, Westerstede, Germany
[5] Univ Roma La Sapienza, Dept Neurol Sci, I-00185 Rome, Italy
[6] Univ Wales Hosp, WERN, Cardiff CF4 4XW, S Glam, Wales
[7] Staffordshire Univ, Dept Neurol, N Staffordshire Royal Infirm, Stoke On Trent ST4 2DE, Staffs, England
[8] Eisai Europe Ltd, Hatfield, Herts, England
[9] Univ Liverpool, Div Neurosci, Liverpool L69 3BX, Merseyside, England
来源
ACTA NEUROLOGICA SCANDINAVICA | 2010年 / 121卷 / 03期
关键词
antiepileptic drugs; epilepsy; quality of life; seizures; treatment; REFRACTORY PARTIAL EPILEPSY; LONG-TERM SAFETY; DOUBLE-BLIND; ANTIEPILEPTIC DRUGS; TRIAL; EFFICACY; THERAPY;
D O I
10.1111/j.1600-0404.2009.01311.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives - To assess the efficacy and tolerability of zonisamide in a study allowing flexible dosing in a more diverse and less refractory population than assessed in randomized controlled trials. Methods - This 19-week, non-comparative study of adjunctive zonisamide included 281 adults who had at least four partial-onset seizures within 8 weeks on one or two antiepileptic drugs. Alterations to zonisamide doses were allowed after titration, except during two fixed-dose periods (weeks 10-13 and 16-19). Results - At the end of the second fixed-dose period (median dose 300 mg/day), the median reduction in monthly seizure frequency was 33.3-41.1%; >= 50% responder rate was 40.9-44.2%; and seizure freedom rate was 15.0-15.9%, depending on the analysis used. The most common adverse events were fatigue (16.7%) and somnolence (15.3%). Conclusions - Zonisamide demonstrated efficacy in a setting more reflective of clinical practice and was generally well tolerated.
引用
收藏
页码:141 / 148
页数:8
相关论文
共 19 条
  • [1] Introduction to zonisamide
    Baulac, M
    [J]. EPILEPSY RESEARCH, 2006, 68 : S3 - S9
  • [2] Data from regulatory studies: what do they tell? What don't they tell?
    Ben-Menachem, E
    [J]. ACTA NEUROLOGICA SCANDINAVICA, 2005, 112 : 21 - 25
  • [3] Clinical pharmacology and mechanism of action of zonisamide
    Biton, Victor
    [J]. CLINICAL NEUROPHARMACOLOGY, 2007, 30 (04) : 230 - 240
  • [4] Brodie MJ, 2005, EPILEPSIA, V46, P31
  • [5] New antiepileptic drugs: Comparison of key clinical trials
    Cramer, JA
    Fisher, R
    Ben-Menachem, E
    French, J
    Mattson, RH
    [J]. EPILEPSIA, 1999, 40 (05) : 590 - 600
  • [6] Randomized controlled trial of zonisamide for the treatment of refractory partial-onset seizures
    Faught, E
    Ayala, R
    Montouris, GG
    Leppik, IE
    [J]. NEUROLOGY, 2001, 57 (10) : 1774 - 1779
  • [7] A double-blind, placebo-controlled study of vigabatrin three g/day in patients with uncontrolled complex partial seizures
    French, JA
    Mosier, M
    Walker, S
    Sommerville, K
    Sussman, N
    Barry, E
    Bell, W
    Bergen, D
    Browne, T
    Ferrendelli, J
    Fisher, R
    Fromm, G
    Homan, R
    Krauss, G
    Lai, CW
    Leppik, I
    Leroy, R
    Pellock, J
    Penovich, P
    Ramsay, RE
    Shinnar, S
    [J]. NEUROLOGY, 1996, 46 (01) : 54 - 61
  • [8] Topiramate monotherapy as broad-spectrum antiepileptic drug in a naturalistic clinical setting
    Guerrini, R
    Carpay, J
    Groselj, J
    van Oene, J
    Schreiner, A
    Lahaye, M
    Schwalen, S
    [J]. SEIZURE-EUROPEAN JOURNAL OF EPILEPSY, 2005, 14 (06): : 371 - 380
  • [9] Comparison of evidence of treatment effects in randomized and nonrandomized studies
    Ioannidis, JPA
    Haidich, AB
    Pappa, M
    Pantazis, N
    Kokori, SI
    Tektonidou, MG
    Contopoulos-Ioannidis, DG
    Lau, J
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (07): : 821 - 830
  • [10] Leppik I, 2006, EPILEPTIC DISORD, V8, P118