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利妥昔单抗治疗继发进展型多发性硬化症的疗效:来自磁共振成像和残疾评估的见解

Efficacy of rituximab in secondary progressive multiple sclerosis: Insights from magnetic resonance imaging and disability assessments.

作者信息

Ashtari Fereshteh, Mokary Yousef, Adibi Iman, Shaygannejad Vahid, Ramezani Neda, Davanian Fariba, Ahmadi Maryam

机构信息

Department of Neurology, Isfahan University of Medical Sciences, Isfahan, Iran.

Isfahan Neurosciences Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

J Res Med Sci. 2025 Jul 24;30:39. doi: 10.4103/jrms.jrms_690_24. eCollection 2025.

Abstract

BACKGROUND

Although there are a few options for the treatment of patients with secondary progressive multiple sclerosis (SPMS), rituximab (RTX) is used as an off-label treatment. This study aimed to investigate the efficacy of RTX on disability status and volumetric magnetic resonance imaging (MRI) findings in SPMS.

MATERIALS AND METHODS

This study was conducted on 31 patients with SPMS treated with RTX 1000 mg intravenously every 6 months. Expanded Disability Status Scale (EDSS), 25-Foot Walk Test (25-FWT), 9-Hole Peg Test (9-HPT), and brain MRI were performed at the baseline and after 12 months.

RESULTS

No significant changes were observed in EDSS, timed 25-FWT, and 9-HPT within 12 months of RTX treatment ( > 0.05). There was a decrease in 9-HPT time in both the right and left hands, but it was not significant. During the 12-month assessment, white matter (WM) and gray matter volumes decreased by -41.48 ± 2.36 and -31.65 ± 8.84, respectively. However, these differences were not statistically significant ( > 0.05). The only significant change was an increase in the volume of deep WM lesions (WMLs) (0.26 ± 0.19 vs. 0.38 ± 0.29, = 0.024). A significant association was found between the EDSS at the 12 month and baseline deep WML volume ( = 0.383, = 0.044).

CONCLUSION

Our results showed that the level of disability based on EDSS, timed 25-FWT, and 9-HPT did not increase significantly during 12 months of treatment with RTX. These findings suggest that RTX may play a role in disease stabilization and preventing disability progression, especially in the upper limbs. Further studies with larger sample sizes are necessary to confirm this finding.

摘要

背景

尽管对于继发进展型多发性硬化症(SPMS)患者有几种治疗选择,但利妥昔单抗(RTX)被用作一种非适应证治疗。本研究旨在调查RTX对SPMS患者残疾状态和容积磁共振成像(MRI)结果的疗效。

材料与方法

本研究对31例接受RTX治疗的SPMS患者进行,每6个月静脉注射1000mg。在基线期和12个月后进行扩展残疾状态量表(EDSS)、25英尺步行试验(25-FWT)、9孔插钉试验(9-HPT)以及脑部MRI检查。

结果

在RTX治疗的12个月内,EDSS、定时25-FWT和9-HPT均未观察到显著变化(P>0.05)。左右手的9-HPT时间均有所下降,但不显著。在12个月的评估中,白质(WM)和灰质体积分别减少了-41.48±2.36和-31.65±8.84。然而,这些差异无统计学意义(P>0.05)。唯一显著的变化是深部WM病变(WMLs)体积增加(0.26±0.19对0.38±0.29,P=0.024)。在12个月时的EDSS与基线深部WML体积之间发现显著相关性(r=0.383,P=0.044)。

结论

我们的结果表明,在RTX治疗的12个月内,基于EDSS、定时25-FWT和9-HPT的残疾水平没有显著增加。这些发现表明,RTX可能在疾病稳定和预防残疾进展中发挥作用,尤其是在上肢。需要更大样本量的进一步研究来证实这一发现。

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