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多发性硬化症的诱导与升级:一项为期 10 年的真实世界研究。

Induction Versus Escalation in Multiple Sclerosis: A 10-Year Real World Study.

机构信息

Department of Neurosciences, S. Camillo-Forlanini Hospital, C.ne Gianicolense 87, 00152, Rome, Italy.

Multiple Sclerosis Centre, ASST Spedali Civili di Brescia, P.O. Montichiari, Via Ciotti 154, 25018, Montichiari, BS, Italy.

出版信息

Neurotherapeutics. 2020 Jul;17(3):994-1004. doi: 10.1007/s13311-020-00847-0.

DOI:10.1007/s13311-020-00847-0
PMID:32236822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7609676/
Abstract

In this independent, multicenter, post-marketing study, we directly compare induction immunosuppression versus escalation strategies on the risk of reaching the disability milestone of Expanded Disability Status Scale (EDSS) ≥ 6.0 over 10 years in previously untreated patients with relapsing-remitting multiple sclerosis. We collected data of patients who started interferon beta (escalation) versus mitoxantrone or cyclophosphamide (induction) as initial treatment. Main eligibility criteria included an EDSS score ≤ 4.0 at treatment start and either ≥ 2 relapses or 1 disabling relapse with evidence of ≥ 1 gadolinium-enhancing lesion at magnetic resonance imaging scan in the pre-treatment year. Since patients were not randomized to treatment group, we performed a propensity score (PS)-based matching procedure to select individuals with homogeneous baseline characteristics. Comparisons were then conducted using Cox models stratified by matched pairs. Overall, 75 and 738 patients started with induction and escalation, respectively. Patients in the induction group were older and more disabled than those in the escalation group (p < 0.05). The PS-matching procedure retained 75 patients per group. In the re-sampled population, a lower proportion of patients reached the outcome after induction (21/75, 28.0%) than escalation (29/75, 38.7%) (hazard ratio = 0.48; p = 0.024). Considering the whole sample, serious adverse events occurred more frequently after induction (8/75, 10.7%) than escalation (18/738, 2.4%) (odds ratio = 3.36, p = 0.015). These findings suggest that, in patients with poor prognostic factors, induction was more effective than escalation in reducing the risk of reaching the disability milestone, albeit with a worse safety profile. Future studies are warranted to explore if newer induction agents may provide a more advantageous long-lasting risk:benefit profile.

摘要

在这项独立的、多中心的上市后研究中,我们直接比较了诱导免疫抑制与递增策略在未经治疗的复发缓解型多发性硬化症患者中,10 年内达到扩展残疾状态量表(EDSS)≥6.0 的残疾里程碑的风险。我们收集了开始使用干扰素β(递增)与米托蒽醌或环磷酰胺(诱导)作为初始治疗的患者的数据。主要入选标准包括治疗开始时 EDSS 评分≤4.0,以及在治疗前 1 年内磁共振成像扫描有≥1 个钆增强病变的证据下,有≥2 次复发或 1 次致残性复发。由于患者未随机分组到治疗组,我们进行了倾向评分(PS)匹配程序以选择基线特征相似的个体。然后使用 Cox 模型按匹配对进行分层比较。共有 75 名和 738 名患者分别开始诱导和递增治疗。诱导组患者年龄较大且残疾程度较重(p<0.05)。PS 匹配程序保留了每组 75 名患者。在重新抽样的人群中,诱导组达到结局的患者比例较低(21/75,28.0%),而递增组为(29/75,38.7%)(风险比=0.48;p=0.024)。考虑到整个样本,诱导组(8/75,10.7%)发生严重不良事件的频率高于递增组(18/738,2.4%)(比值比=3.36,p=0.015)。这些发现表明,在预后不良的患者中,与递增策略相比,诱导策略在降低达到残疾里程碑的风险方面更有效,尽管安全性较差。需要进一步研究探索新型诱导药物是否能提供更有利的长期风险获益比。

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