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奥瑞珠单抗可减缓原发性进展型多发性硬化症患者上肢功能障碍的进展:来自 III 期随机 ORATORIO 试验的结果。

Ocrelizumab reduces progression of upper extremity impairment in patients with primary progressive multiple sclerosis: Findings from the phase III randomized ORATORIO trial.

机构信息

Central Texas Neurology Consultants and Dell Medical School, The University of Texas at Austin, Round Rock, TX, USA.

Department of Neurology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.

出版信息

Mult Scler. 2018 Dec;24(14):1862-1870. doi: 10.1177/1352458518808189. Epub 2018 Nov 12.

DOI:10.1177/1352458518808189
PMID:30415593
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6282157/
Abstract

BACKGROUND

Upper extremity (UE) impairment is common with primary progressive multiple sclerosis (PPMS).

OBJECTIVE

This exploratory analysis examined the effects of ocrelizumab on confirmed progression (CP) and confirmed improvement (CI) in UE impairment in patients from ORATORIO.

METHODS

Patients with PPMS received ocrelizumab 600 mg or placebo every 24 weeks for ⩾120 weeks. The Nine-Hole Peg Test (9HPT) was administered at baseline (BL) and every 12 weeks thereafter. Prespecified exploratory endpoints included change in 9HPT time and proportion of patients with CP of ⩾20% in 9HPT. Analysis populations included intention-to-treat (ITT) patients and subgroups stratified by BL 9HPT time and Expanded Disability Status Scale. Post hoc analyses included the proportion of patients achieving more severe thresholds of CP and the proportion achieving CI in 9HPT.

RESULTS

Among ITT patients, ocrelizumab significantly reduced the change in 9HPT time over 120 weeks, the risk of CP of ⩾20% in 9HPT time for both hands and the risk of more severe 9HPT progression versus placebo. Numerical trends also favoured ocrelizumab versus placebo with respect to achieving CI. Consistent directional trends were observed in subgroup analyses.

CONCLUSION

Ocrelizumab reduces the risk of UE disability progression and may increase the possibility of improvement versus placebo in PPMS.

摘要

背景

原发性进展型多发性硬化症(PPMS)患者常出现上肢(UE)功能障碍。

目的

本探索性分析旨在研究奥瑞珠单抗对 ORATORIO 研究中患者 UE 功能障碍确认进展(CP)和确认改善(CI)的影响。

方法

PPMS 患者接受奥瑞珠单抗 600mg 或安慰剂,每 24 周 1 次,共 120 周以上。在基线(BL)和此后每 12 周进行 9 孔钉测试(9HPT)。预先指定的探索性终点包括 9HPT 时间的变化和 9HPT 时间 CP ⩾20%的患者比例。分析人群包括意向治疗(ITT)患者和按 BL 9HPT 时间和扩展残疾状况量表分层的亚组。事后分析包括达到更严重 CP 阈值的患者比例和在 9HPT 中达到 CI 的患者比例。

结果

在 ITT 患者中,奥瑞珠单抗在 120 周内显著减少了 9HPT 时间的变化,双手 9HPT 时间 CP ⩾20%的风险以及与安慰剂相比更严重的 9HPT 进展的风险。与安慰剂相比,奥瑞珠单抗在实现 CI 方面也呈现出数值趋势的优势。亚组分析中观察到一致的方向性趋势。

结论

奥瑞珠单抗降低了 UE 残疾进展的风险,并可能增加与安慰剂相比改善的可能性,适用于 PPMS 患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5681/6282157/1e134e2fb3ad/10.1177_1352458518808189-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5681/6282157/8a496044f454/10.1177_1352458518808189-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5681/6282157/1e134e2fb3ad/10.1177_1352458518808189-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5681/6282157/8a496044f454/10.1177_1352458518808189-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5681/6282157/1e134e2fb3ad/10.1177_1352458518808189-fig2.jpg

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