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停止米托蒽醌治疗 10 年后复发进展型多发性硬化症 411 例的临床随访:真实队列研究。

Clinical follow-up of 411 patients with relapsing and progressive multiple sclerosis 10 years after discontinuing mitoxantrone treatment: a real-life cohort study.

机构信息

Department of Neurology, Nancy University Hospital, Nancy, France.

CIC-EC Inserm 1433, Vandoeuvre-Lès-Nancy, France.

出版信息

Eur J Neurol. 2018 Dec;25(12):1439-1445. doi: 10.1111/ene.13748. Epub 2018 Aug 3.

Abstract

BACKGROUND AND PURPOSE

Mitoxantrone (MITOX) has been used to treat patients with aggressive multiple sclerosis (MS) for decades. We aimed to describe the effectiveness and adverse events over 10 years post-MITOX in patients with relapsing and progressive MS from an exhaustive real-life database.

METHODS

Data from patients who received MITOX before 1 January 2006 were collected from the MS Lorraine registry. Expanded Disability Status Scale (EDSS) scores and annual relapse rates (ARRs) year by year during follow-up and the year prior to MITOX were compared. Time to the first relapse and a 1-point increase in EDSS score were used in Cox multivariate models to find associations with potential predictive factors.

RESULTS

A total of 411 patients were included. The ARR for the 155 relapsing patients had decreased from 2.0 (SD 1.20) the year before treatment to 0.3 (SD 0.31) by year 10 (P < 0.0001). The EDSS score increased from 2.8 (SD 1.44) to 4.8 (SD 1.90) by year 10 (P < 0.0001). A high ARR at MITOX initiation was associated with a longer time to a 1-point increase in EDSS score (hazard ratio, 0.81; 95% confidence interval, 0.67-0.99; P = 0.04). The EDSS score in 256 progressive patients increased from 5.0 (SD 1.33) to 6.5 (SD 1.26) by year 10 (P < 0.0001). We identified four cases of acute myeloid leukemias.

CONCLUSIONS

Patients with the most active forms of MS are the most likely to benefit from MITOX in the long term.

摘要

背景与目的

米托蒽醌(MITOX)已被用于治疗侵袭性多发性硬化症(MS)患者数十年。我们旨在描述在接受米托蒽醌治疗 10 年后复发和进行性 MS 患者的有效性和不良反应,使用的是详尽的真实世界数据库。

方法

从 MS 洛林登记处收集了在 2006 年 1 月 1 日前接受米托蒽醌治疗的患者的数据。比较了随访期间和治疗前一年的扩展残疾状态量表(EDSS)评分和年复发率(ARR)。使用 Cox 多变量模型,根据潜在的预测因素,对首次复发时间和 EDSS 评分增加 1 分进行了分析。

结果

共纳入 411 例患者。155 例复发患者的 ARR 从治疗前的 2.0(SD 1.20)下降到第 10 年的 0.3(SD 0.31)(P < 0.0001)。EDSS 评分从 2.8(SD 1.44)增加到第 10 年的 4.8(SD 1.90)(P < 0.0001)。米托蒽醌治疗开始时高 ARR 与 EDSS 评分增加 1 分的时间延长相关(危险比,0.81;95%置信区间,0.67-0.99;P = 0.04)。256 例进行性患者的 EDSS 评分从 5.0(SD 1.33)增加到第 10 年的 6.5(SD 1.26)(P < 0.0001)。我们发现了 4 例急性髓系白血病病例。

结论

最活跃的 MS 患者最有可能从米托蒽醌的长期治疗中受益。

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