Dimethyl Fumarate Delays Multiple Sclerosis in Radiologically Isolated Syndrome

安慰剂 医学 富马酸二甲酯 临床终点 危险系数 多发性硬化 临床孤立综合征 不利影响 置信区间 内科学 临床试验 随机对照试验 比例危险模型 病理 免疫学 替代医学
作者
Darin T. Okuda,Orhun H. Kantarci,Christine Lebrun‐Frenay,Maria Pia Sormani,Christina Azevedo,Francesca Bovis,Le H. Hua,Lilyana Amezcua,Ellen M. Mowry,Christophe Hotermans,Jason P. Mendoza,John Walsh,Christian von Hehn,Wendy Vargas,Stacy Donlon,Robert T. Naismith,Annette Okai,Gabriel Pardo,Pavle Repovic,Olaf Stüve,Aksel Sıva,Daniel Pelletier
出处
期刊:Annals of Neurology [Wiley]
卷期号:93 (3): 604-614 被引量:20
标识
DOI:10.1002/ana.26555
摘要

The radiologically isolated syndrome (RIS) represents the earliest detectable pre-clinical phase of multiple sclerosis (MS). This study evaluated the impact of therapeutic intervention in preventing first symptom manifestation at this stage in the disease spectrum.We conducted a multi-center, randomized, double-blinded, placebo-controlled study involving people with RIS. Individuals without clinical symptoms typical of MS but with incidental brain MRI anomalies consistent with central nervous system (CNS) demyelination were included. Within 12 MS centers in the United States, participants were randomly assigned 1:1 to oral dimethyl fumarate (DMF) 240 mg twice daily or placebo. The primary endpoint was the time to onset of clinical symptoms attributable to a CNS demyelinating event within a follow-up period of 96 weeks. An intention-to-treat analysis was applied to all participating individuals in the primary and safety investigations. The study is registered at ClinicalTrials.gov, NCT02739542 (ARISE).Participants from 12 centers were recruited from March 9, 2016, to October 31, 2019, with 44 people randomized to dimethyl fumarate and 43 to placebo. Following DMF treatment, the risk of a first clinical demyelinating event during the 96-week study period was highly reduced in the unadjusted Cox proportional-hazards regression model (hazard ratio [HR] = 0.18, 95% confidence interval [CI] = 0.05-0.63, p = 0.007). More moderate adverse reactions were present in the DMF (34 [32%]) than placebo groups (19 [21%]) but severe events were similar (DMF, 3 [5%]; placebo, 4 [9%]).This is the first randomized clinical trial demonstrating the benefit of a disease-modifying therapy in preventing a first acute clinical event in people with RIS. ANN NEUROL 2023;93:604-614.
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