Therapy response prediction of focal cortex stimulation based on clinical parameters: a multicentre, non-interventional study protocol.

IF 2.3 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL BMJ Open Pub Date : 2025-02-16 DOI:10.1136/bmjopen-2024-089903
Sotirios Kalousios, Jürgen Hesser, Matthias Dümpelmann, Christoph Baumgartner, Hajo M Hamer, Martin Hirsch, Lukas Imbach, Elisabeth Kaufmann, Josua Kegele, Susanne Knake, Georg Leonhardt, Thomas Mayer, Ann Mertens, Ekaterina Pataraia, Felix von Podewils, Carlos M Quesada, Bernhard J Steinhoff, Rainer Surges, Berthold R Voges, Jan Wagner, Yvonne G Weber, Tim Wehner, Yaroslav Winter, Andreas Schulze-Bonhage
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Abstract

Introduction: A novel focal cortex stimulation (FCS) device has recently received approval in Europe for patients with focal drug-resistant epilepsy (DRE). After 6 months of stimulation, 17 of 32 patients achieved ≥50% reduction in seizure frequency compared with their prestimulation baseline (responders). Currently, there is no established method for predicting FCS treatment response prior to implantation.

Methods and analysis: This is an ongoing combined retrospective-prospective non-interventional multicentre study. Clinical data of up to 100 patients treated with FCS are collected across 20 collaborating epilepsy centres in four European countries. The key outcome parameters, seizure frequency and severity, are measured along with metrics on cognition, mood and quality of life, both pre-electrode and postelectrode implantation. The data are complemented by demographics, medical history and information on antiseizure medication and FCS treatment parameters during the stimulation period. In addition to clinical data, MRI and electroencephalography registrations are used to gain insights into spatial and electrophysiological aspects of FCS. Multivariate statistical and machine learning analyses are employed to identify key predictive biomarkers associated with patient outcomes (responders vs non-responders). The primary goal is to improve counselling for DRE patients by identifying promising candidates for FCS treatment.

Ethics and dissemination: This study has received approval from the ethics committee of the University of Freiburg, Germany (23-1540 S1; 23-1183_1-S1-retro). The same approval is applicable for all participating centres in Germany as part of a multicentre study. Ghent University Hospital, Belgium, has received approval for participation in the retrospective arm from their local ethics committee (ONZ-2024-0168). The final approvals for the participating Swiss and Austrian sites are still pending. The results will be made available to the public through peer-reviewed journals and conference presentations.

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基于临床参数的局灶性皮质刺激的治疗反应预测:一项多中心、非介入性研究方案。
一种新的局灶性皮质刺激(FCS)装置最近在欧洲获得批准,用于局灶性耐药癫痫(DRE)患者。刺激6个月后,32例患者中有17例与刺激前基线相比癫痫发作频率降低≥50%(应答者)。目前,还没有确定的方法来预测植入前FCS治疗的反应。方法和分析:这是一项正在进行的回顾性-前瞻性非介入性多中心联合研究。在四个欧洲国家的20个合作癫痫中心收集了多达100名接受FCS治疗的患者的临床数据。主要结局参数,癫痫发作频率和严重程度,以及电极植入前和电极植入后的认知、情绪和生活质量指标进行测量。这些数据还补充了人口统计学、病史和刺激期间抗癫痫药物和FCS治疗参数的信息。除了临床数据外,MRI和脑电图记录也用于了解FCS的空间和电生理方面。采用多变量统计和机器学习分析来确定与患者结果相关的关键预测性生物标志物(反应者与无反应者)。主要目标是通过确定有希望的FCS治疗候选人来改善对DRE患者的咨询。伦理与传播:本研究已获得德国弗莱堡大学伦理委员会的批准(23-1540 S1;23 - 1183 _1 - s1 -复古)。作为多中心研究的一部分,同样的批准适用于德国的所有参与中心。比利时根特大学医院已获得当地伦理委员会批准参与回顾性研究(ONZ-2024-0168)。瑞士和奥地利的最终批准仍在等待中。研究结果将通过同行评议的期刊和会议报告向公众公布。
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来源期刊
BMJ Open
BMJ Open MEDICINE, GENERAL & INTERNAL-
CiteScore
4.40
自引率
3.40%
发文量
4510
审稿时长
2-3 weeks
期刊介绍: BMJ Open is an online, open access journal, dedicated to publishing medical research from all disciplines and therapeutic areas. The journal publishes all research study types, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Publishing procedures are built around fully open peer review and continuous publication, publishing research online as soon as the article is ready.
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