Dang Chun, Lu Yaoheng, Xiong Ying
Department of Periodical Press/Chinese Evidence-Based Medicine Center, West China Hospital, Sichuan University, Chengdu, China.
Department of General Surgery, Chengdu Integrated Traditional Chinese Medicine and Western Medicine Hospital, Chengdu, China.
Neurol Sci. 2025 Aug 18. doi: 10.1007/s10072-025-08392-4.
Progressive multiple sclerosis (PMS) remains a therapeutic challenge, with limited effective treatments and a high degree of uncertainty surrounding long-term efficacy and safety. In this context, the recently published Cochrane network meta-analysis by Ridley et al. (2024) represents a significant effort to synthesise available evidence on immunomodulatory and immunosuppressive therapies in PMS. This article provides a structured summary and critical commentary on the findings of the Cochrane review. It highlights key clinical insights, evidence gaps, and methodological limitations that have implications for practice and future research. Based on data from 23 randomised controlled trials involving over 10,000 participants, the Cochrane review reported modest relapse-reducing effects for rituximab and interferon beta-1b. However, no interventions demonstrated consistent or high-certainty evidence for delaying disability progression. Interferon beta-1a was associated with a higher rate of treatment discontinuation due to adverse events. Notably, the majority of studies had short follow-up durations and did not assess health-related quality of life. Our commentary underscores the limited clinical impact of current therapies in PMS and the persistent uncertainty in the evidence base. We advocate for more robust, independent trials incorporating longer follow-up, head-to-head comparisons, and standardised, patientcentred outcome reporting. We also call attention to the need for better integration of real-world data to improve the applicability of trial findings. This Cochrane review provides timely and methodologically sound evidence on pharmacological management in PMS. However, the overall modest benefits observed reinforce the urgent need for high-quality, patient-focused research to guide future therapeutic development and clinical decision-making.
进行性多发性硬化症(PMS)仍然是一个治疗难题,有效治疗方法有限,且长期疗效和安全性存在高度不确定性。在此背景下,里德利等人(2024年)最近发表的Cochrane网络荟萃分析代表了一项重大努力,旨在综合PMS免疫调节和免疫抑制疗法的现有证据。本文对Cochrane综述的结果进行了结构化总结和批判性评论。它突出了对实践和未来研究有影响的关键临床见解、证据空白和方法学局限性。基于23项涉及10000多名参与者的随机对照试验数据,Cochrane综述报告了利妥昔单抗和干扰素β-1b在降低复发方面有适度效果。然而,没有干预措施显示出在延缓残疾进展方面有一致或高度确定的证据。干扰素β-1a因不良事件导致治疗中断的发生率较高。值得注意的是,大多数研究的随访时间较短,且未评估与健康相关的生活质量。我们的评论强调了当前疗法对PMS的临床影响有限以及证据基础中持续存在的不确定性。我们主张进行更有力、独立的试验,纳入更长时间的随访、直接比较以及标准化、以患者为中心的结果报告。我们还提请注意需要更好地整合真实世界数据,以提高试验结果的适用性。这项Cochrane综述为PMS的药物管理提供了及时且方法学合理的证据。然而,观察到的总体适度益处强化了对高质量、以患者为重点的研究的迫切需求,以指导未来的治疗发展和临床决策。