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那他珠单抗可改善复发缓解型多发性硬化症患者的行走能力:前瞻性TIMER研究及AFFIRM回顾性分析结果

Natalizumab improves ambulation in relapsing-remitting multiple sclerosis: results from the prospective TIMER study and a retrospective analysis of AFFIRM.

作者信息

Voloshyna N, Havrdová E, Hutchinson M, Nehrych T, You X, Belachew S, Hotermans C, Paes D

机构信息

Institute of Neurology, Psychiatry and Narcology NAMS of Ukraine, Kharkiv, Ukraine.

出版信息

Eur J Neurol. 2015 Mar;22(3):570-7. doi: 10.1111/ene.12618. Epub 2014 Dec 15.

Abstract

BACKGROUND AND PURPOSE

Impaired ambulation is a prominent disabling symptom of multiple sclerosis and can lead to reduced quality of life. Whether natalizumab, a monoclonal antibody shown to reduce disease activity in relapsing-remitting multiple sclerosis, could impact ambulation performance was examined.

METHODS

A prospective open-label study, TIMER, was conducted in natalizumab-naive patients (n = 215). The timed 25-foot walk (T25FW) and timed 100-m walk (T100MW) were assessed at baseline and at weeks 24 and 48 of natalizumab therapy, together with Expanded Disability Status Scale scores. The effects of natalizumab on T25FW performance were also examined in a retrospective analysis of natalizumab-treated patients (n = 627) and placebo control patients (n = 315) from the AFFIRM study.

RESULTS

In TIMER, a significant increase from baseline in T25FW speed was seen at week 24 (P = 0.0074) and in T100MW speed at weeks 24 and 48 (both P < 0.001). A greater proportion of patients showed clinically meaningful increases (≥20%) in walking speed on the T100MW (25%) than on the T25FW (13%) at week 48 (P = 0.032). In AFFIRM, natalizumab increased the proportion of patients with ≥20% confirmed improvement in T25FW speed at year 2 by 78% versus placebo (P = 0.0133).

CONCLUSIONS

Natalizumab increased walking speed in patients with relapsing-remitting multiple sclerosis. The T100MW may be more sensitive to changes in ambulation capacity than the T25FW, and both tests appear to detect clinically meaningful improvements in ambulatory function.

摘要

背景与目的

行走功能障碍是多发性硬化症的一个突出致残症状,可导致生活质量下降。本研究旨在探讨那他珠单抗(一种已证实可降低复发缓解型多发性硬化症疾病活动度的单克隆抗体)是否会影响行走能力。

方法

对215例未使用过那他珠单抗的患者进行了一项前瞻性开放标签研究(TIMER)。在基线时以及那他珠单抗治疗的第24周和第48周,评估了25英尺定时步行试验(T25FW)、100米定时步行试验(T100MW)以及扩展残疾状态量表评分。还对来自AFFIRM研究的那他珠单抗治疗患者(n = 627)和安慰剂对照患者(n = 315)进行了回顾性分析,以研究那他珠单抗对T25FW表现的影响。

结果

在TIMER研究中,第24周时T25FW速度较基线显著增加(P = 0.0074),第24周和第48周时T100MW速度均显著增加(均P < 0.001)。在第48周时,T(100MW)上显示行走速度有临床意义增加(≥20%)的患者比例(25%)高于T25FW(13%)(P = 0.032)。在AFFIRM研究中,与安慰剂相比,那他珠单抗使第2年T25FW速度确认改善≥20%的患者比例增加了78%(P = 0.0133)。

结论

那他珠单抗可提高复发缓解型多发性硬化症患者的行走速度。T100MW可能比T25FW对行走能力变化更敏感,并且这两项测试似乎都能检测到行走功能有临床意义的改善。

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