依维莫司治疗局灶性皮质发育不良 2 型患者的疗效和安全性。

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY Epilepsia Open Pub Date : 2024-11-28 DOI:10.1002/epi4.13104
Se Hee Kim, Hoon-Chul Kang, Yun Ho Roh, Jongsung Hahn, Kyung Lok Min, Seok-Jin Lee, Donghwa Yang, Han Som Choi, Soyoung Park, Jeong Ho Lee, Sang-Guk Lee, Se Hoon Kim, Min Jung Chang, Heung Dong Kim
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引用次数: 0

摘要

研究目的本研究旨在评估依维莫司治疗局灶性皮质发育不良2型(FCD 2)相关癫痫发作的有效性和安全性:一项前瞻性、交叉、安慰剂对照临床试验(ClinicalTrials.gov:NCT03198949)招募了年龄在4-40岁之间、病理确诊为FCD 2型、在筛查前3个月中有2个月每月癫痫发作次数≥3次的患者。试验包括一个为期 4 周的基线阶段、两个为期 12 周的核心阶段和一个为期 29 周的扩展阶段。患者在核心阶段I以盲法接受依维莫司或安慰剂治疗,在核心阶段II交叉接受替代治疗。依维莫司的用量为4.5毫克/平方米/天,目标血清水平为5-15纳克/毫升。主要结果是在每个核心阶段的最后一个月,癫痫发作较基线减少≥50%的患者比例。对各组间的安全性进行了比较:2017年5月11日至2020年6月19日期间,21名患者完成了核心阶段的治疗。依维莫司组和安慰剂组的主要结果无明显差异(24% vs. 19%,p = 0.66)。患者的反应各不相同。3名MTOR基因有致病变异或无基因异常的患者在核心阶段的最后一个月使用依维莫司后癫痫不再发作,而其他基因有变异的患者则无一发作。依维莫司治疗过程中出现粘膜炎或皮肤溃疡等不良事件的几率更高(19/21 vs. 7/21,p):与安慰剂相比,依维莫司治疗12周在减少癫痫发作方面并未显示出整体优势。不过,它在大多数 MTOR 基因致病变异患者中显示出了前景,这突出表明有必要进一步研究影响治疗反应的患者特异性因素。依维莫司治疗总体上是安全和可控的。白话摘要:这项研究测试了依维莫司对减少局灶性皮质发育不良2型(FCD 2)患者癫痫发作的作用。虽然对大多数患者来说,依维莫司并不比安慰剂更有效,但也有少数患者显示出更好的疗效,其中一些患者已不再出现癫痫发作。副作用很常见,但可以控制。要了解为什么某些患者对治疗反应更好,还需要进行更多的研究。
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Efficacy and safety of everolimus for patients with focal cortical dysplasia type 2

Objective

This study aimed to evaluate the effectiveness and safety of everolimus in treating seizures associated with focal cortical dysplasia type 2 (FCD 2).

Methods

A prospective, crossover, placebo-controlled clinical trial (ClinicalTrials.gov: NCT03198949) enrolled patients aged 4–40 years with pathologically confirmed FCD 2 and a history of ≥3 seizures per month for two out of the 3 months prior to screening. The trial included a 4-week baseline phase, two 12-week core phases, and a 29-week extension phase. Patients received everolimus or placebo in a blinded manner during core phase I, with crossover to the alternate treatment in core phase II. Everolimus dosage started at 4.5 mg/m2/day, targeting a serum level of 5–15 ng/mL. The primary outcome was the proportion of patients achieving ≥50% seizure reduction from baseline in the last month of each core phase. Safety profiles were compared between groups.

Results

Between May 11, 2017, and June 19, 2020, 21 patients completed the core phases. There was no significant difference in the primary outcome between everolimus and placebo groups (24% vs. 19%, p = 0.66). The patients showed varied responses. Three patients with a pathogenic variant in the MTOR gene or no genetic abnormalities achieved seizure freedom with everolimus in the last month of the core phase, while none of the patients with variants in other genes did. Adverse events, such as mucositis or skin ulceration, were more common with everolimus (19/21 vs. 7/21, p < 0.001). All adverse events resolved without study drug withdrawal.

Significance

Everolimus treatment for 12 weeks did not show overall superiority in reducing seizures compared to placebo. However, it showed promise, mostly in patients with a pathogenic variant in the MTOR gene, highlighting the need for further research into patient-specific factors influencing treatment response. The everolimus treatment was generally safe and manageable.

Plain Language Summary

This study tested everolimus for reducing seizures in patients with focal cortical dysplasia type 2 (FCD 2). While the drug was not more effective than a placebo for most, few patients showed better results, with some becoming seizure-free. Side effects were common but manageable. More research is needed to understand why certain patients respond better to treatment.

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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
期刊最新文献
Efficacy and tolerability of low versus standard daily doses of antiseizure medications in newly diagnosed focal epilepsy. A multicenter, randomized, single-blind, non-inferiority trial (STANDLOW). Three cases of atypical Rasmussen's encephalitis with delayed-onset seizures. GATAD2B-related developmental and epileptic encephalopathy (DEE): Extending the epilepsy phenotype and a literature appraisal. Intrinsic brain network stability during kainic acid-induced epileptogenesis. Diagnostic yield of utilizing 24-72-hour video electroencephalographic monitoring in the diagnosis of seizures presenting as paroxysmal events in resource-limited settings.
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