Adjunctive zonisamide therapy in the long-term treatment of children with partial epilepsy: Results of an open-label extension study of a phase III, randomized, double-blind, placebo-controlled trial

被引:32
作者
Guerrini, Renzo [1 ]
Rosati, Anna [1 ]
Bradshaw, Kate [2 ]
Giorgi, Luigi [2 ]
机构
[1] Univ Florence, Childrens Hosp Anna Meyer, Dept Neurosci Pharmacol & Child Hlth, Pediat Neurol Unit & Labs, I-50139 Florence, Italy
[2] Eisai Ltd, Hatfield, Herts, England
关键词
Partial seizures; Pediatric epilepsy; Growth; Development; Zonisamide; Safety/tolerability; ADD-ON THERAPY; PARTIAL SEIZURES; PUBERTAL CHANGES; CLASSIFICATION; VIGABATRIN; PATTERN;
D O I
10.1111/epi.12548
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective To investigate the safety/tolerability and efficacy of long-term adjunctive zonisamide and its impact on growth and development in children (6-18years) with partial epilepsy. Methods Open-label extension of a phase III, placebo-controlled trial. Started with double-blind transition period (2-11weeks), during which patients on zonisamide continued at the same dose and those on placebo switched to zonisamide 1mg/kg/day, up-titrated to 8mg/kg/day (maximum 500mg/day). During the subsequent open-label period (45-57weeks), zonisamide dosing could be adjusted according to tolerability/response. Safety assessments included treatment-emergent adverse events (TEAEs), clinical laboratory parameters, and vital signs. Efficacy assessments included responder rate (primary assessment) and seizure freedom rate during the open-label period. Growth and development assessments comprised Tanner stages, hand x-rays, Child Behavior Checklist (CBCL 6/18), School Performance questionnaire, Physician and Parent/Guardian Global Impression of Change, and Controlled Oral Word Association Test (COWAT). Results One hundred forty-four children entered the study; 99 (68.8%) of 144 children completed it, and 108 (75.0%) of 144 received zonisamide for >= 1year. TEAEs occurred in 39 (27.1%) of 144 patients. There were low incidences of serious TEAEs (2.1%) and TEAEs leading to discontinuation (2.8%). Bicarbonate level decreases >3.5mm occurred in 64 patients (44.4%), and 24 patients (16.7%) had a weight decrease of >= 10% from baseline. During the open-label period, 81 (56.3%) of 144 patients were responders and 16 (11.1%) of 144 achieved seizure freedom. Tanner staging and skeletal development were as expected for the study population. Changes were minimal for CBCL 6/18 and School Performance scores. Most patients were "much improved"/"very much improved" on Physician (73.8%) and Parent/Guardian (75.4%) Global Impressions of Change. Median changes in COWAT Category and Letter Fluency scores were 2.0 and 0.5, respectively. Significance Adjunctive zonisamide was well tolerated and efficacious over a period of at least 1year in children with partial epilepsy, with no unexpected safety concerns and no consistent detrimental effects on growth and development. A PowerPoint slide summarizing this article is available for download in the Supporting Information section .
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页码:568 / 578
页数:11
相关论文
共 24 条
[1]  
[Anonymous], HLTH TECHNOL ASSESS
[2]  
[Anonymous], 2012, ZON PRESCR INF
[3]  
[Anonymous], 2013, ZON SUMM PROD CHAR
[4]   Gabapentin as add-on therapy in children with refractory partial seizures: A 12-week, multicentre, double-blind, placebo-controlled study [J].
Appleton, R ;
Fichtner, K ;
Lamoreaux, L ;
Alexander, J ;
Halsall, G ;
Murray, G ;
Garofalo, E .
EPILEPSIA, 1999, 40 (08) :1147-1154
[5]   Efficacy and tolerability of zonisamide versus controlled-release carbamazepine for newly diagnosed partial epilepsy: a phase 3, randomised, double-blind, non-inferiority trial [J].
Baulac, Michel ;
Brodie, Martin J. ;
Patten, Anna ;
Segieth, Joanna ;
Giorgi, Luigi .
LANCET NEUROLOGY, 2012, 11 (07) :579-588
[6]   Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009 [J].
Berg, Anne T. ;
Berkovic, Samuel F. ;
Brodie, Martin J. ;
Buchhalter, Jeffrey ;
Cross, J. Helen ;
Boas, Walter van Emde ;
Engel, Jerome ;
French, Jacqueline ;
Glauser, Tracy A. ;
Mathern, Gary W. ;
Moshe, Solomon L. ;
Nordli, Douglas ;
Plouin, Perrine ;
Scheffer, Ingrid E. .
EPILEPSIA, 2010, 51 (04) :676-685
[7]   Clinical pharmacology and mechanism of action of zonisamide [J].
Biton, Victor .
CLINICAL NEUROPHARMACOLOGY, 2007, 30 (04) :230-240
[8]   Antiepileptic drug development in children - Considerations for a revisited strategy [J].
Chiron, Catherine ;
Dulac, Olivier ;
Pons, Gerard .
DRUGS, 2008, 68 (01) :17-25
[9]  
Connock M, 2006, HEALTH TECHNOL ASSES, V10, pIII
[10]   A placebo-controlled trial of lamotrigine add-on therapy for partial seizures in children [J].
Duchowny, M ;
Pellock, JM ;
Graf, WD ;
Billard, C ;
Gilman, J ;
Casale, E ;
Womble, G ;
Risner, M ;
Manasco, P .
NEUROLOGY, 1999, 53 (08) :1724-1731