van den Munckhof Bart, Arzimanoglou Alexis, Perucca Emilio, van Teeseling Heleen C, Leijten Frans S S, Braun Kees P J, Jansen Floor E
Department of Paediatric Neurology, Brain Center, University Medical Center Utrecht, Member of the European Reference Network EpiCARE, Utrecht University, KC 03.063.0, PO Box 85090, 3508 AB, Utrecht, The Netherlands.
Paediatric Clinical Epileptology, Sleep Disorders and Functional Neurology Department, University Hospitals of Lyon (HCL), Coordinator of the European Reference Network EpiCARE, Lyon Neurosciences Research Centre, Lyon, France.
Trials. 2020 Nov 23;21(1):957. doi: 10.1186/s13063-020-04874-2.
Epileptic encephalopathy with electrical status epilepticus in sleep (ESES) is an epilepsy syndrome occurring almost exclusively in children, usually at an age between 4 and 12 years. It is characterised by abundant sleep-induced epileptic activity in the electroencephalogram (EEG) and by acquired cognitive and behavioural deficits. The goal of treatment is to prevent further decline or even improve cognitive functioning. Based on mostly small and retrospective studies, corticosteroids and clobazam are regarded by many clinicians as the most effective pharmacological treatments. This European multicentre randomised controlled trial is designed to compare the effects of corticosteroids and clobazam on cognitive functioning after 6 months. Secondary outcomes include cognitive functioning after 18 months, EEG abnormalities in sleep, safety and tolerability, and seizure frequency. We also aimed at investigating whether treatment response in epileptic encephalopathy with ESES can be predicted by measurement of inflammatory mediators and autoantibodies in serum.
The pragmatic study will be performed in centres with expertise in the treatment of rare paediatric epilepsy syndromes across Europe. A total of 130 patients, 2 to 12 years of age, with epileptic encephalopathy with ESES will be enrolled and randomised in a 1:1 ratio to receive either corticosteroids (monthly intravenous methylprednisolone pulses or daily oral prednisolone) or oral clobazam for 6 months according to an open-label parallel-group design. Follow-up visits with clinical assessment, EEGs, and neuropsychological testing are scheduled for up to 18 months. Blood samples for cytokine and autoantibody testing are obtained before treatment and 8 months after treatment initiation.
The treatment of epileptic encephalopathy with ESES aims at improving cognitive outcome. This randomised controlled study will compare the most frequently used treatments, i.e. corticosteroids and clobazam. If the study proves superiority of one treatment over the other or identifies biomarkers of treatment response, results will guide clinicians in the early treatment of this severe epilepsy syndrome.
ISRCTN, ISRCTN42686094 . Registered on 24 May 2013.
伴睡眠中癫痫性电持续状态的癫痫性脑病(ESES)是一种几乎仅发生于儿童的癫痫综合征,通常发病年龄在4至12岁之间。其特征为脑电图(EEG)中出现大量睡眠诱发的癫痫活动以及获得性认知和行为缺陷。治疗目标是防止认知功能进一步下降甚至改善认知功能。基于大多为小型回顾性研究,许多临床医生认为皮质类固醇和氯巴占是最有效的药物治疗方法。这项欧洲多中心随机对照试验旨在比较皮质类固醇和氯巴占在6个月后对认知功能的影响。次要结局包括18个月后的认知功能、睡眠中的脑电图异常、安全性和耐受性以及癫痫发作频率。我们还旨在研究是否可以通过测量血清中的炎症介质和自身抗体来预测伴ESES的癫痫性脑病的治疗反应。
这项实用性研究将在欧洲各地具有罕见小儿癫痫综合征治疗专业知识的中心进行。总共130名年龄在2至12岁之间、患有伴ESES的癫痫性脑病的患者将被纳入研究,并按1:1的比例随机分组,根据开放标签平行组设计接受皮质类固醇(每月静脉注射甲泼尼龙脉冲或每日口服泼尼松龙)或口服氯巴占治疗6个月。计划进行长达18个月的随访,包括临床评估、脑电图检查和神经心理学测试。在治疗前和治疗开始后8个月采集血液样本进行细胞因子和自身抗体检测。
伴ESES的癫痫性脑病的治疗旨在改善认知结局。这项随机对照研究将比较最常用的治疗方法,即皮质类固醇和氯巴占。如果该研究证明一种治疗方法优于另一种治疗方法或确定治疗反应的生物标志物,研究结果将指导临床医生对这种严重癫痫综合征进行早期治疗。
ISRCTN,ISRCTN42686094。于2013年5月24日注册。