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芬氟拉明治疗德雷维特综合征:长期真实世界分析显示安全性及医疗负担减轻。

Fenfluramine treatment for Dravet syndrome: Long term real-world analysis demonstrates safety and reduced health care burden.

作者信息

Boncristiano Alessandra, Balestrini Simona, Doccini Viola, Specchio Nicola, Pietrafusa Nicola, Trivisano Marina, Darra Francesca, Cossu Alberto, Battaglia Domenica, Quintiliani Michela, Gambardella M Luigia, Parente Eliana, Monni Rita, Matricardi Sara, Marini Carla, Ragona Francesca, Granata Tiziana, Striano Pasquale, Riva Antonella, Guerrini Renzo

机构信息

Department of Neuroscience and Medical Genetics, Children's Hospital Meyer IRCCS, Florence, Italy.

Neurofarba Department, University of Florence, Florence, Italy.

出版信息

Epilepsia. 2025 Apr;66(4):1110-1118. doi: 10.1111/epi.18241. Epub 2024 Dec 30.

Abstract

OBJECTIVE

Fenfluramine (FFA), stiripentol (STP), and cannabidiol (CBD) are approved add-on therapies for seizures in Dravet syndrome (DS). We report on the long-term safety and health care resource utilization (HCRU) of patients with DS treated with FFA under an expanded access program (EAP).

METHODS

A cohort of 124 patients received FFA for a median of 2.8 years (34.4 months). We compared data on safety and HCRU during FFA treatment with those from a same pre-treatment period. Echocardiography was conducted every 6 months. Information collected included gender, age, and auxological parameters (height, weight, and body mass index [BMI]) at the start (T0) and follow-up (T1); FFA treatment details (start, withdrawal, dosage); adverse events (AEs); and HCRU data including hospital admissions, status epilepticus (SE) episodes, and rescue medication use. We grouped patients by weight: ≤37.4 kg (n = 68, 54.8%) and ≥37.5 kg (n = 56; 45.1%), with FFA dosing adjusted accordingly. Statistical analyses included paired t test, Wilcoxon signed-rank test, Kaplan-Meier analysis, and Bonferroni correction to adjust for multiple testing.

RESULTS

Mean age was 47 months at clinical diagnosis and 81 months at T0. The last follow-up average FFA dose was .5 mg/kg/day, with a median of .4 mg/kg/day. FFA led to a 9.5% reduction in prior treatment load. At last follow-up, 118 of 124 (91.5%) remained on FFA. Rescue medication use decreased significantly from 4.5 to 1, hospitalizations from 1 to 0, and SE episodes from 0-240 to 0-180 (p < .001 for all). Seizure freedom was achieved in 9 of 118 patients (7.6%). AEs occurred in 39 of 124 patients (31.5%), with no cardiac issues or deaths. There was an overall mean reduction in BMI, with no statistical significance, and never requiring FFA withdrawal.

SIGNIFICANCE

FFA is well tolerated, without cardiac toxicity, and reduces treatment load and HCRU, suggesting improved patient management. BMI reduction in young children highlights the need for growth and nutritional monitoring.

摘要

目的

芬氟拉明(FFA)、司替戊醇(STP)和大麻二酚(CBD)是已获批用于治疗Dravet综合征(DS)癫痫发作的附加疗法。我们报告了在扩大准入计划(EAP)下接受FFA治疗的DS患者的长期安全性和医疗资源利用(HCRU)情况。

方法

一组124例患者接受FFA治疗,中位治疗时间为2.8年(34.4个月)。我们将FFA治疗期间的安全性和HCRU数据与同一治疗前期的数据进行了比较。每6个月进行一次超声心动图检查。收集的信息包括开始治疗时(T0)和随访时(T1)的性别、年龄和生长学参数(身高、体重和体重指数[BMI]);FFA治疗细节(开始、停药、剂量);不良事件(AE);以及HCRU数据,包括住院、癫痫持续状态(SE)发作和急救药物使用情况。我们根据体重将患者分组:≤37.4 kg(n = 68,54.8%)和≥37.5 kg(n = 56;45.1%),并相应调整FFA剂量。统计分析包括配对t检验、Wilcoxon符号秩检验、Kaplan-Meier分析以及用于校正多重检验的Bonferroni校正。

结果

临床诊断时的平均年龄为47个月,T0时为81个月。最后一次随访时FFA的平均剂量为0.5 mg/kg/天,中位剂量为0.4 mg/kg/天。FFA使先前的治疗负担降低了9.5%。在最后一次随访时,124例患者中有118例(91.5%)仍在使用FFA。急救药物的使用从4.5次显著减少至1次,住院次数从1次减少至0次,SE发作次数从0 - 240次减少至0 - 180次(所有p值均<0.001)。118例患者中有9例(7.6%)实现了无癫痫发作。124例患者中有39例(31.5%)发生了AE,未出现心脏问题或死亡。BMI总体平均有所下降,但无统计学意义,且从未因该原因停用FFA。

意义

FFA耐受性良好,无心脏毒性,可降低治疗负担和HCRU,表明患者管理得到改善。幼儿BMI降低凸显了生长和营养监测的必要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aea8/11997923/cf58255df9f4/EPI-66-1110-g001.jpg

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