Treatment Response to Antiseizure Medications in People With Newly Diagnosed Focal Epilepsy.

IF 21.3 1区 医学 Q1 CLINICAL NEUROLOGY
Sarah N Barnard, Zhibin Chen, Manisha Holmes, Andres M Kanner, Manu Hegde, Ruben Kuzniecky, Daniel Lowenstein, Jacqueline A French
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引用次数: 0

Abstract

Importance: Epilepsy affects approximately 65 million people worldwide, and 60% have focal seizures. Predicting seizure response and drug resistance to antiseizure medications (ASMs) in people with focal epilepsy remains difficult.

Objective: To describe the expected short- and long-term response to treatment with ASMs in people with focal epilepsy using recognized definitions by the International League Against Epilepsy.

Design, setting, and participants: The Human Epilepsy Project is an international, prospective, observational cohort study that followed up people with newly diagnosed focal epilepsy for up to 6 years between 2012 and 2020. Data were analyzed from 2023 to 2024. The Human Epilepsy Project was conducted at 34 tertiary epilepsy centers across the US, Australia, and Europe. Participants with confirmed diagnosis of focal epilepsy aged 12 to 60 years were enrolled within 4 months of treatment initiation with ASM(s). Data were analyzed from February 2024 to July 2024.

Exposure: ASM (variable).

Main outcomes and measures: The primary outcome was seizure freedom, defined as a period without seizures for 12 months or 3 times the longest pretreatment seizure-free interval, whichever was longer. Treatment response was categorized as sensitive, meaning seizure free receiving 2 or fewer adequate ASM trials; resistant, meaning having 2 or more adequate ASM trials fail; or indeterminate (neither treatment sensitive nor resistant).

Results: Among 448 enrolled participants, 267 (59.6%) were female, and median (IQR) participant age was 32 (21-44) years at treatment initiation. Median (IQR) follow-up duration was 3.13 (2.33-3.55) years. Most achieved seizure freedom (267 participants of 448 [59.6%]), largely without relapse (223 [83.5%]). There were 245 treatment-sensitive participants (54.7%), 102 treatment-resistant participants (22.8%), and 101 indeterminate participants (22.5%). Among treatment-sensitive participants, most (217 [89.3%]) responded to monotherapy and half (121 [49.4%], or 27% of total cohort) became seizure free while receiving their first ASM. In the first year of treatment, 251 participants (63%) had ongoing or worsening seizures. Median time to first seizure freedom was 12.1 months (95% CI, 9.7-16.1). This occurred earlier in those who never relapsed (median, 2.2 months; 95% CI, 0.8-3.2) than those who did (median, 7.4 months; 95% CI, 4.0-10.7). Those with infrequent pretreatment seizures were 0.41-fold more likely to be treatment resistant than those with very frequent seizures (relative risk [RR], 0.41; 95% CI, 0.18-0.89; P = .03; HB-corrected P = .02). Participants with self-reported comorbid psychological disorders were 1.78-fold more likely to be treatment resistant than those without (RR, 1.78; 95% CI, 1.26-2.52; P = .001).

Conclusions and relevance: In the Human Epilepsy Project multicenter prospective cohort study, most people with newly diagnosed focal epilepsy took more than a year and more than 1 ASM to become seizure free. Drug resistance can be identified earlier in those with frequent pretreatment seizures, and a history of psychiatric comorbidities at epilepsy diagnosis is an important prognostic factor.

Trial registration: ClinicalTrials.gov Identifier: NCT02126774.

新诊断局灶性癫痫患者抗癫痫药物治疗反应
重要性:全世界约有6500万人患有癫痫,其中60%为局灶性癫痫发作。预测局灶性癫痫患者的癫痫发作反应和抗癫痫药物耐药性仍然很困难。目的:根据国际抗癫痫联盟认可的定义,描述局灶性癫痫患者抗痉挛药物治疗的预期短期和长期反应。设计、环境和参与者:人类癫痫项目是一项国际性、前瞻性、观察性队列研究,在2012年至2020年期间对新诊断的局灶性癫痫患者进行了长达6年的随访。数据分析时间为2023年至2024年。人类癫痫项目在美国、澳大利亚和欧洲的34个三级癫痫中心进行。确诊为局灶性癫痫的12至60岁的参与者在ASM治疗开始的4个月内入组。数据分析时间为2024年2月至2024年7月。暴露:ASM(变量)。主要结局和指标:主要结局为无癫痫发作,定义为12个月无癫痫发作或3倍于最长的预处理无癫痫发作间隔,以较长的为准。治疗反应被归类为敏感,即接受2次或更少的充分的ASM试验后无癫痫发作;耐药,意味着有2个或更多的ASM试验失败;或不确定(既不敏感也不耐药)。结果:在448名入组参与者中,267名(59.6%)为女性,治疗开始时参与者的中位年龄(IQR)为32岁(21-44岁)。中位(IQR)随访时间为3.13(2.33-3.55)年。大多数患者(448例患者中267例[59.6%])实现癫痫发作自由,大部分患者无复发(223例[83.5%])。治疗敏感者245人(54.7%),治疗耐药者102人(22.8%),不确定者101人(22.5%)。在治疗敏感的参与者中,大多数(217[89.3%])对单药治疗有反应,一半(121[49.4%],或总队列的27%)在接受首次ASM时无癫痫发作。在治疗的第一年,251名参与者(63%)持续或恶化癫痫发作。到首次发作自由的中位时间为12.1个月(95% CI, 9.7-16.1)。这种情况在从未复发的患者中(中位数,2.2个月;95% CI, 0.8-3.2)比复发的患者(中位数,7.4个月;95% CI, 4.0-10.7)发生得更早。不频繁发作的患者比频繁发作的患者耐药的可能性高0.41倍(相对危险度[RR], 0.41; 95% CI, 0.18-0.89; P = 0.03; hb校正P = 0.02)。自我报告有共病性心理障碍的受试者出现治疗抵抗的可能性是无共病性心理障碍患者的1.78倍(RR, 1.78; 95% CI, 1.26-2.52; P = .001)。结论及相关性:在人类癫痫项目(Human Epilepsy Project)的多中心前瞻性队列研究中,大多数新诊断为局灶性癫痫的患者需要一年多的时间和超过1个ASM才能恢复无癫痫发作。耐药可以在那些频繁的前处理癫痫发作中更早被发现,癫痫诊断时的精神合并症史是一个重要的预后因素。试验注册:ClinicalTrials.gov标识符:NCT02126774。
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来源期刊
JAMA neurology
JAMA neurology CLINICAL NEUROLOGY-
CiteScore
41.90
自引率
1.70%
发文量
250
期刊介绍: JAMA Neurology is an international peer-reviewed journal for physicians caring for people with neurologic disorders and those interested in the structure and function of the normal and diseased nervous system. The Archives of Neurology & Psychiatry began publication in 1919 and, in 1959, became 2 separate journals: Archives of Neurology and Archives of General Psychiatry. In 2013, their names changed to JAMA Neurology and JAMA Psychiatry, respectively. JAMA Neurology is a member of the JAMA Network, a consortium of peer-reviewed, general medical and specialty publications.
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