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探索自体造血干细胞移植治疗进展性多发性硬化症的潜力——系统评价。

Exploring the therapeutic potential of autologous hematopoietic stem cell transplantation in progressive multiple sclerosis-a systematic review.

机构信息

Institute of Neuroimmunology and Multiple Sclerosis, University Medical Centre Hamburg-Eppendorf, Hamburg, Germany.

Department of Stem Cell Transplantation, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.

出版信息

Eur J Neurol. 2024 Dec;31(12):e16427. doi: 10.1111/ene.16427. Epub 2024 Aug 5.

Abstract

BACKGROUND AND PURPOSE

The aim was to determine the value of autologous haematopoietic stem cell transplantation (aHSCT) as a therapeutic intervention for progressive multiple sclerosis (PMS) based on a systematic review of the current literature.

METHODS

All studies from the databases PubMed and Google Scholar published in English before February 2024 which provided individual data for PMS patients were systematically reviewed. PICO was defined as population (P), primary progressive MS and secondary progressive MS patients; intervention (I), treatment with aHSCT; comparison (C), none, disease-modifying therapy treated/relapsing-remitting MS cohorts if available; outcome (O), transplant-related mortality, progression-free survival (PFS) and no evidence of disease activity.

RESULTS

A total of 15 studies met the criteria including 665 patients with PMS (74 primary progressive MS, 591 secondary progressive MS) and 801 patients with relapsing-remitting MS as controls. PFS data were available for 647 patients. PMS patients showed more severe disability at baseline than relapsing-remitting MS patients. The average transplant-related mortality for PMS in 10 studies was 1.9%, with 10 deaths in 528 patients. PFS ranged from 0% to 78% in PMS groups 5 years after treatment initiation, demonstrating a high variability. No evidence of disease activity scores at 5 years ranged from 0% to 75%.

CONCLUSION

Based on the available data, aHSCT does not halt progression in people with PMS. However, there appears to be evidence of improved outcome in selected patients. Due to the heterogeneity of the available data, more comprehensive clinical trials assessing the efficacy of aHSCT across different patient groups are urgently needed to reduce variability and improve patient stratification.

摘要

背景与目的

本研究旨在通过对当前文献的系统回顾,确定自体造血干细胞移植(aHSCT)作为治疗进展型多发性硬化症(PMS)的价值。

方法

系统检索了 PubMed 和 Google Scholar 数据库中截至 2024 年 2 月前发表的所有英文研究,这些研究为 PMS 患者提供了个体数据。定义了 PICO 人群(P)为原发性进展型 MS 和继发性进展型 MS 患者;干预措施(I)为 aHSCT 治疗;对照组(C)为无、疾病修正治疗的患者/缓解-复发型 MS 队列(如适用);结局(O)为移植相关死亡率、无进展生存率(PFS)和无疾病活动证据。

结果

共有 15 项研究符合标准,包括 665 例 PMS 患者(74 例原发性进展型 MS,591 例继发性进展型 MS)和 801 例缓解-复发型 MS 患者作为对照组。647 例患者可提供 PFS 数据。与缓解-复发型 MS 患者相比,PMS 患者基线时的残疾程度更严重。10 项研究中 PMS 的平均移植相关死亡率为 1.9%,528 例患者中有 10 例死亡。治疗后 5 年 PMS 组的 PFS 范围为 0%至 78%,显示出很高的变异性。5 年时无疾病活动评分范围为 0%至 75%。

结论

根据现有数据,aHSCT 不能阻止 PMS 患者的进展。然而,在一些选定的患者中似乎有改善结局的证据。由于现有数据的异质性,迫切需要更全面的临床试验来评估不同患者群体中 aHSCT 的疗效,以减少变异性并改善患者分层。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ab/11555148/6621886946fb/ENE-31-e16427-g001.jpg

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