Early Intensive Versus Escalation Approach: Ten-Year Impact on Disability in Relapsing Multiple Sclerosis.

IF 3.9 2区 医学 Q1 CLINICAL NEUROLOGY
Pietro Iaffaldano, Giuseppe Lucisano, Tommaso Guerra, Francesca Caputo, Marta Simone, Massimiliano Copetti, Damiano Paolicelli, Emilio Portaccio, Francesco Patti, Paola Perini, Vincenzo Brescia Morra, Alessia Di Sapio, Matilde Inglese, Carlo Pozzilli, Giacomo Lus, Giuseppe Salemi, Erica Curti, Giovanna De Luca, Paola Valentino, Eleonora Cocco, Paola Cavalla, Carlo Avolio, Alessandra Lugaresi, Antonio Gallo, Pietro Annovazzi, Maria A Rocca, Clara Grazia Chisari, Massimo Filippi, Maria Pia Amato, Maria Trojano
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Abstract

Objective: To evaluate the long-term impact of early intensive treatment (EIT) versus escalation (ESC) strategies using high-efficacy disease-modifying therapies (HE-DMTs) on disability progression in relapsing multiple sclerosis (RMS).

Methods: This observational study included 4878 RMS patients from the Italian Multiple Sclerosis Register. Eligible participants initiated their first disease-modifying therapy (DMT) within 3 years of disease onset and had ≥ 5 years of follow-up with at least three Expanded Disability Status Scale (EDSS) evaluations. Patients were categorized into the EIT group if they started with HE-DMTs and into the ESC group if HE-DMTs were initiated after ≥ 1 year of moderate-efficacy therapy. Propensity score matching was performed to balance baseline characteristics. Outcomes included disability trajectories assessed using linear mixed models for repeated measures and risks of confirmed disability accrual (CDA), progression independent of relapse activity (PIRA), and relapse-associated worsening (RAW) evaluated using Cox proportional hazards models.

Results: Post-matching analysis of 908 pairs revealed significantly slower disability progression in the EIT group compared to the ESC group. At 10 years, the delta-EDSS difference between groups was -0.63 (95% CI: -0.83 to -0.43; p < 0.0001). ESC was associated with higher risks of CDA (HR 1.36, 95% CI: 1.20-1.54; p < 0.0001), PIRA (HR 1.22, 95% CI: 1.05-1.40; p = 0.0074), and RAW (HR 1.55, 95% CI: 1.17-2.05; p = 0.0021).

Interpretation: EIT significantly reduces long-term disability progression in RMS compared to ESC. These findings underscore the potential of EIT to optimize long-term outcomes in RMS patients.

早期强化治疗与升级治疗:复发性多发性硬化症患者10年的残疾影响。
目的:评估早期强化治疗(EIT)与使用高效疾病改善疗法(he - dmt)的升级(ESC)策略对复发性多发性硬化症(RMS)残疾进展的长期影响。方法:这项观察性研究包括4878名来自意大利多发性硬化症登记册的RMS患者。符合条件的参与者在发病3年内开始首次疾病改善治疗(DMT),随访≥5年,至少进行3次扩展残疾状态量表(EDSS)评估。如果患者开始接受he - dmt治疗,则分为EIT组;如果患者在接受中等疗效治疗≥1年后开始接受he - dmt治疗,则分为ESC组。进行倾向评分匹配以平衡基线特征。结果包括使用重复测量的线性混合模型评估残疾轨迹,以及使用Cox比例风险模型评估确认残疾累积(CDA)、独立于复发活动的进展(PIRA)和复发相关恶化(RAW)的风险。结果:908对配对后分析显示,与ESC组相比,EIT组的残疾进展明显减慢。10年时,两组间δ - edss差异为-0.63 (95% CI: -0.83 ~ -0.43;p解释:与ESC相比,EIT显著减少了RMS的长期残疾进展。这些发现强调了EIT优化RMS患者长期预后的潜力。
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来源期刊
Annals of Clinical and Translational Neurology
Annals of Clinical and Translational Neurology Medicine-Neurology (clinical)
CiteScore
9.10
自引率
1.90%
发文量
218
审稿时长
8 weeks
期刊介绍: Annals of Clinical and Translational Neurology is a peer-reviewed journal for rapid dissemination of high-quality research related to all areas of neurology. The journal publishes original research and scholarly reviews focused on the mechanisms and treatments of diseases of the nervous system; high-impact topics in neurologic education; and other topics of interest to the clinical neuroscience community.
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