BRIVA-ONE study: 12-month outcomes of brivaracetam monotherapy in clinical practice

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY
Epilepsia Open Pub Date : 2024-10-29 DOI:10.1002/epi4.13078
Vicente Villanueva, Esther González Villar, Alejandro Fernandez-Cabrera, Jorge Zurita, Francisco J. Lopez-Gonzalez, Xiana Rodríguez-Osorio, Beatriz Parejo-Carbonell, José C. Estevez, Blanca Mercedes-Alvarez, Joaquín Ojeda, Marta Rubio-Roy, Alexandre Garcia-Escrivá, Asier Gómez-Ibáñez, Javier Martinez-Poles, Paula Martinez-Agredano, Raquel Calle, Alba Sierra-Marcos, Ana M. Gonzalez, José D. Herrera, Juan Rodriguez-Uranga, Beatriz Cabezas, Emilio Martinez, Julia Renau, María de Toledo, Kevin G. Hampel, Cristina Alarcón, María Inés Barceló, Angela Monterde, Lidia B. Lara, Gemma Sansa, José M. Serratosa
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引用次数: 0

Abstract

Objective

This study investigated the effectiveness and tolerability of brivaracetam (BRV) monotherapy in a large series of patients with epilepsy.

Method

This was a multicenter, retrospective, observational, non-interventional study in 24 hospitals across Spain. Patients aged ≥18 years who started on BRV monotherapy, either as first-line or following conversion, at least 1 year before database closure were included. Patients were evaluated at baseline and at 3, 6 and 12 months after initiation of BRV monotherapy, in accordance with usual clinical practice at these centers. Data were collected retrospectively from patients' individual charts by participating physicians. The primary effectiveness and safety endpoints were the percentage of seizure-free patients 1 year after initiation of BRV monotherapy and the proportion of patients reporting adverse events (AEs) over the complete follow-up period. Retention rates and subpopulation analysis (levetiracetam switchers, elderly and different etiologies) were also investigated.

Results

A total of 276 patients were included (48 with BRV as first-line monotherapy and 228 who converted to BRV monotherapy). The overall retention rate in monotherapy at 12 months was 89.9% (87.5% for first-line monotherapy group; 90.4% for conversion-to-monotherapy group). Seizure-freedom rates at 12 months were 77.8% (75% for first-line monotherapy group; 78.4% for conversion-to-monotherapy group). AEs occurred in 39.5% of patients at 12 months (35.4% for first-line monotherapy group; 40.4% for conversion-to-monotherapy group). Most AEs were mild-to-moderate. The most frequent AEs were irritability (12.3%) and dizziness (10.1%). The most frequent AEs leading to BRV withdrawal were dizziness (1.8%) and memory problems (1.4%). Similar outcomes in terms of effectiveness and tolerability of BRV monotherapy were observed in patients switching from levetiracetam, those with different epilepsy etiologies, and elderly patients.

Significance

BRV was effective and well tolerated both as first-line monotherapy and following conversion to monotherapy in a real-world setting of patients with epilepsy.

Plain Language Summary

The goal of the medical treatment of epilepsy is to ensure best possible patient quality of life, by maximizing seizure control and minimizing medication toxicity. Brivaracetam (BRV) is a new-generation epilepsy treatment that is well tolerated by patients. In our study, monotherapy with BRV reduced seizures in patients who had not received other treatments and in patients who switched from a previous treatment to BRV monotherapy. BRV was well tolerated and also effective in sensitive patients (i.e., the elderly and those who had epilepsy caused by a brain tumor or a brain injury).

Abstract Image

BRIVA-ONE 研究:临床实践中rivaracetam单药治疗的12个月疗效。
目的:本研究调查了大量癫痫患者接受溴伐他西泮单药治疗的有效性和耐受性:本研究调查了大量癫痫患者接受溴伐他西泮 (BRV) 单一疗法的有效性和耐受性:这是一项多中心、回顾性、观察性、非干预性研究,在西班牙的 24 家医院进行。纳入的患者年龄≥18 岁,在数据库关闭前至少 1 年开始接受 BRV 单药治疗,无论是一线治疗还是转换治疗。根据这些中心的常规临床实践,对患者进行了基线评估以及开始 BRV 单一疗法后 3、6 和 12 个月的评估。数据由参与研究的医生从患者的个人病历中回顾性收集。主要的有效性和安全性终点是开始BRV单药治疗1年后无癫痫发作患者的比例,以及在整个随访期间报告不良事件(AE)的患者比例。此外,还对保留率和亚人群分析(左乙拉西坦转换者、老年人和不同病因)进行了调查:共纳入 276 例患者(48 例接受 BRV 一线单药治疗,228 例转为 BRV 单药治疗)。单药治疗 12 个月的总体保留率为 89.9%(一线单药治疗组为 87.5%;转为单药治疗组为 90.4%)。12个月时摆脱癫痫发作的比例为77.8%(一线单药治疗组为75%;转为单药治疗组为78.4%)。12个月时,39.5%的患者出现了不良反应(一线单药治疗组为35.4%;转为单药治疗组为40.4%)。大多数不良反应为轻度至中度。最常见的不良反应是烦躁(12.3%)和头晕(10.1%)。导致停用 BRV 的最常见不良反应是头晕(1.8%)和记忆问题(1.4%)。从左乙拉西坦转入BRV单药治疗的患者、不同癫痫病因的患者和老年患者的有效性和耐受性结果相似:在癫痫患者的真实世界中,BRV作为一线单药治疗和转为单药治疗的疗效和耐受性都很好。布里瓦西坦(Brivaracetam,BRV)是新一代癫痫治疗药物,患者耐受性良好。在我们的研究中,BRV 单一疗法可减少未接受过其他治疗的患者以及从之前的治疗转为 BRV 单一疗法的患者的癫痫发作。BRV对敏感患者(即老年人和因脑肿瘤或脑损伤导致癫痫的患者)具有良好的耐受性和疗效。
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
Epilepsia Open
Epilepsia Open Medicine-Neurology (clinical)
CiteScore
4.40
自引率
6.70%
发文量
104
审稿时长
8 weeks
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