自体造血干细胞移植治疗多发性硬化症后疗效的相关因素。

IF 8.7 1区 医学 Q1 CLINICAL NEUROLOGY
Yassine Noui, Christina Zjukovskaja, Thomas Silfverberg, Per Ljungman, Kim Kultima, Andreas Tolf, Tobias Tolf, Kristina Carlson, Joachim Burman
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引用次数: 0

摘要

背景:自体造血干细胞移植(AHSCT)已成为复发-缓解型多发性硬化症(RRMS)的一种非常有效的治疗方法,尽管患者选择仍然具有挑战性。疾病修饰疗法(dmt)和手术相关并发症对治疗结果的影响程度尚不清楚。本研究的目的是探讨可能影响AHSCT后预后的因素。方法:分析来自瑞典多中心回顾性队列研究造血干细胞移植治疗多发性硬化症(AutoMS-Swe)的数据,该研究包括174名在2020年1月1日之前接受AHSCT的RRMS患者。主要结局包括炎症性疾病活动性、确认的残疾恶化(CDW)和疾病活动性的总体证据。确认的残疾改善作为次要结果进行调查。使用单变量Cox比例风险模型评估感兴趣变量与结果之间的关联。结果:AHSCT前接受利妥昔单抗作为最后一次DMT的患者炎症性疾病活动的风险降低(HR 0.18, 95% CI 0.04至0.78)。Epstein-Barr病毒检测与炎症性疾病活动的高风险相关(HR 2.3, 95% CI 1.05 ~ 5.07)。CDW与较长的病程相关(HR 1.09, 95% CI 1.00 ~ 1.19),与钆增强病变负相关(HR 0.08, 95% CI 0.01 ~ 0.64)。未接受治疗的患者未发生CDW事件。结论:先前的利妥昔单抗治疗似乎对AHSCT后的炎症活性具有保护作用。疾病持续时间和钆增强病变是AHSCT后残疾的主要决定因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factors associated with outcomes following autologous haematopoietic stem cell transplantation for multiple sclerosis.

Background: Autologous haematopoietic stem cell transplantation (AHSCT) has emerged as a highly effective treatment for relapsing-remitting multiple sclerosis (RRMS), though patient selection remains challenging. The degree to which disease-modifying therapies (DMTs) and procedure-related complications affect treatment outcomes is unclear. The objective of this study was to investigate the factors that might influence outcomes following AHSCT.

Methods: Data from the multicentre, retrospective cohort study Haematopoietic Stem Cell Transplantation for Treatment of Multiple Sclerosis in Sweden (AutoMS-Swe) were analysed, comprising 174 patients with RRMS who received AHSCT before 1 January 2020. Primary outcomes included inflammatory disease activity, confirmed disability worsening (CDW) and overall evidence of disease activity. Confirmed disability improvement was investigated as a secondary outcome. Associations between variables of interest and outcomes were assessed using univariable Cox proportional hazards models.

Results: Patients who received rituximab as the last DMT before AHSCT had a reduced hazard of inflammatory disease activity (HR 0.18, 95% CI 0.04 to 0.78). Epstein-Barr virus detection was associated with a higher hazard of inflammatory disease activity (HR 2.3, 95% CI 1.05 to 5.07). CDW was associated with longer disease durations (HR 1.09, 95% CI 1.00 to 1.19) and was negatively associated with gadolinium-enhancing lesions (HR 0.08, 95% CI 0.01 to 0.64). No CDW events occurred in treatment-naive patients.

Conclusions: Prior rituximab treatment appears to be protective against inflammatory activity after AHSCT. Disease duration and gadolinium-enhancing lesions are major determinants of disability following AHSCT.

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来源期刊
CiteScore
15.70
自引率
1.80%
发文量
888
审稿时长
6 months
期刊介绍: The Journal of Neurology, Neurosurgery & Psychiatry (JNNP) aspires to publish groundbreaking and cutting-edge research worldwide. Covering the entire spectrum of neurological sciences, the journal focuses on common disorders like stroke, multiple sclerosis, Parkinson’s disease, epilepsy, peripheral neuropathy, subarachnoid haemorrhage, and neuropsychiatry, while also addressing complex challenges such as ALS. With early online publication, regular podcasts, and an extensive archive collection boasting the longest half-life in clinical neuroscience journals, JNNP aims to be a trailblazer in the field.
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