First clinical post-approval, observational study to assess clinical safety and effectiveness of brivaracetam sustained-release formulation in real-life settings of India: BEAM study

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY Seizure-European Journal of Epilepsy Pub Date : 2025-02-01 DOI:10.1016/j.seizure.2025.01.011
Lakshmi Narasimhan Ranganathan , Girish Kulkarni , Ashutosh Kakkad , Krishnaprasad Korukonda , Narendra Chouksey
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Abstract

Purpose

Brivaracetam (BRV) sustained-release (SR) tablets have recently been approved to treat focal seizures in India. SR formulations enhance patient adherence and quality of life (QoL). We assessed safety and effectiveness of BRV-SR for epilepsy management in Indian real-life settings.

Methods

A post-approval observational study involving 1989 patients receiving BRV-SR from 181 centres were analysed. Primary endpoints are efficacy variables derived from seizure-related changes, and secondary endpoints include responder rate (≥50% reduction in focal-onset seizures [FoS]/focal-to-bilateral tonic-clonic seizures [FBTCS] frequency), usage pattern data, clinician's global impression on efficacy index (CGI-EI) and safety variables.

Results

Patients’ mean age was 42.33±12.33 years, and 1441 (72.44%) were men. Psychiatric comorbidities included depression (21.97%), sleep disturbance (15.54%), and anxiety (9.60%). The predominant seizure types were FoS (71.44%) and FBTCS (28.56%). BRV-SR 100 mg once-daily was most prescribed dose (57.37%) at baseline and follow-up visits (51.94%). Median seizure frequency decreased from 2 at baseline to 1 at follow-up visit. At follow-up, 72.1% patients were responders, and 63.75% were seizure-free. BRV-SR showed “marked” to “moderate” improvement in 92.99% of patients according to CGI-EI. Subgroup-analysis revealed a positive correlation between BRV-SR use in patients with drug-resistant epilepsy, psychiatric co-morbidities, and behavioural adverse events (AEs) with past anti-seizure medications. AEs were rare, with none reported in 97.39% patients during study period.

Conclusion

The BEAM study findings provide first real-world evidence on effectiveness and safety of BRV-SR in Indian real-life settings. Furthermore, BRV-SR is a feasible option for focal epilepsy management with good retention rates and improved QoL.
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首个临床批准后的观察性研究,评估布瓦西坦缓释制剂在印度现实环境中的临床安全性和有效性:BEAM研究。
目的:布瓦西坦(BRV)缓释片最近被批准用于治疗局灶性癫痫发作在印度。SR制剂可提高患者依从性和生活质量(QoL)。我们评估了BRV-SR在印度现实环境中用于癫痫管理的安全性和有效性。方法:对来自181个中心接受BRV-SR治疗的1989例患者的批准后观察性研究进行分析。主要终点是源于癫痫相关变化的疗效变量,次要终点包括反应率(局灶性癫痫发作[FoS]减少≥50% /局灶-双侧强直-阵挛性癫痫发作[FBTCS]频率)、使用模式数据、临床医生对疗效指数(CGI-EI)的总体印象和安全性变量。结果:患者平均年龄42.33±12.33岁,男性1441例(72.44%)。精神病学合并症包括抑郁(21.97%)、睡眠障碍(15.54%)和焦虑(9.60%)。主要癫痫类型为FoS(71.44%)和FBTCS(28.56%)。BRV-SR 100mg每日一次是基线和随访时的最大处方剂量(57.37%)。中位发作频率从基线时的2次降至随访时的1次。随访时,72.1%的患者有反应,63.75%的患者无癫痫发作。根据CGI-EI, 92.99%的患者BRV-SR表现为“显著”至“中度”改善。亚组分析显示,BRV-SR在耐药癫痫、精神共病和行为不良事件(ae)患者中的使用与既往抗癫痫药物呈正相关。研究期间,97.39%的患者未报告不良事件。结论:BEAM研究结果为BRV-SR在印度现实生活中的有效性和安全性提供了第一个真实世界的证据。此外,BRV-SR是局灶性癫痫治疗的可行选择,具有良好的保留率和改善的生活质量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Seizure-European Journal of Epilepsy
Seizure-European Journal of Epilepsy 医学-临床神经学
CiteScore
5.60
自引率
6.70%
发文量
231
审稿时长
34 days
期刊介绍: Seizure - European Journal of Epilepsy is an international journal owned by Epilepsy Action (the largest member led epilepsy organisation in the UK). It provides a forum for papers on all topics related to epilepsy and seizure disorders.
期刊最新文献
Corrigendum to “Predictive performances of STESS and EMSE in a Norwegian adult status epilepticus cohort” [Seizure 70 (2019) 6-11] A call for better information about epilepsy: The next of kin perspective Alterations in white matter integrity and correlations with clinical characteristics in children with non-lesional temporal lobe epilepsy Presenteeism in people with previous and current epilepsy: Determinants and psychosocial associations Performance validity tests in people with epilepsy: A review of the literature
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