Lefort Mathilde, Vukusic Sandra, Casey Romain, Edan Gilles, Leray Emmanuelle
Univ Rennes, EHESP, CNRS, Inserm, Arènes - UMR 6051, RSMS (Recherche sur les Services et Management en Santé) - U 1309, Rennes, France.
Univ Rennes, CHU Rennes, Inserm, CIC 1414 [(Centre d'Investigation Clinique de Rennes)], Rennes, France, 35000.
Eur J Neurol. 2022 May 26;29(9):2761-71. doi: 10.1111/ene.15422.
Therapeutic management of relapsing-remitting multiple sclerosis (RRMS) has evolved towards early treatment. The objective was to assess the impact of early treatment initiation on disability progression among RRMS first-line treated patients.
This study included all incident RRMS cases starting interferon or glatiramer acetate for the first time from 1996/01/01 to 2012/31/12 (N=5,279) from ten MS expert OFSEP centers (Observatoire Français de la Sclérose en Plaques). The delay from treatment start to attain an irreversible Expanded Disability Status Scale score of 3.0 were compared between "Early" group (N= 1,882; treated within 12 months following MS clinical onset) and "Later" group using propensity score weighted Kaplan-Meier methods, overall and stratified by age.
Overall, the restricted mean time before reaching EDSS 3.0 (RMST) from treatment start was 11 years and two months for patients treated within the year following MS clinical onset and 10 years and seven months for patients treated later. Thus, early treated patients gained 7 months (95% CI: [4-11] months) in the time to reach EDSS 3.0 compared to patients treated later (treatment start delayed by 28 months). The difference in RMST was respectively six months (95% CI: [1-10] months) and 14 months (95% CI: [4-24] months) in the "≤40 years" age group and in the ">40 years" age group, in favour of early group. .
Early treatment initiation resulted in a significant reduction of disability progression among patients with RRMS, and also among older patients.
复发缓解型多发性硬化症(RRMS)的治疗管理已朝着早期治疗发展。目的是评估早期开始治疗对RRMS一线治疗患者残疾进展的影响。
本研究纳入了1996年1月1日至2012年12月31日首次开始使用干扰素或醋酸格拉替雷的所有RRMS新发病例(N = 5279),这些病例来自十个法国多发性硬化症观察中心(OFSEP)(法国斑块状硬化症观察站)。使用倾向评分加权的Kaplan-Meier方法,比较了“早期”组(N = 1882;在MS临床发病后12个月内接受治疗)和“晚期”组从开始治疗到达到不可逆的扩展残疾状态量表评分3.0的延迟时间,整体以及按年龄分层比较。
总体而言,MS临床发病后一年内接受治疗的患者从开始治疗到达到EDSS 3.0的受限平均时间(RMST)为11年零2个月,而晚期治疗的患者为10年零7个月。因此,与晚期治疗的患者相比(治疗开始延迟28个月),早期治疗的患者在达到EDSS 3.0的时间上提前了7个月(95% CI:[4 - 11]个月)。在“≤40岁”年龄组和“>40岁”年龄组中,RMST的差异分别为6个月(95% CI:[1 - 10]个月)和14个月(95% CI:[4 - 24]个月),均有利于早期治疗组。
早期开始治疗可显著降低RRMS患者以及老年患者的残疾进展。