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进展性多发性硬化症的临床试验:进展、新教训和遗留挑战。

Clinical trials for progressive multiple sclerosis: progress, new lessons learned, and remaining challenges.

机构信息

Queen Square Multiple Sclerosis Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK; Medical Research Council Clinical Trials Unit at UCL, Institute of Clinical Trials and Methodology, University College London, London, UK; National Institute for Health Research, University College London Hospitals, Biomedical Research Centre, London, UK.

Queen Square Multiple Sclerosis Centre, Department of Neuroinflammation, UCL Queen Square Institute of Neurology, Faculty of Brain Sciences, University College London, London, UK.

出版信息

Lancet Neurol. 2024 Mar;23(3):277-301. doi: 10.1016/S1474-4422(24)00027-9.

Abstract

Despite the success of disease-modifying treatments in relapsing multiple sclerosis, for many individuals living with multiple sclerosis, progressive disability continues to accrue. How to interrupt the complex pathological processes underlying progression remains a daunting and ongoing challenge. Since 2014, several immunomodulatory approaches that have modest but clinically meaningful effects have been approved for the management of progressive multiple sclerosis, primarily for people who have active inflammatory disease. The approval of these drugs required large phase 3 trials that were sufficiently powered to detect meaningful effects on disability. New classes of drug, such as Bruton tyrosine-kinase inhibitors, are coming to the end of their trial stages, several candidate neuroprotective compounds have been successful in phase 2 trials, and innovative approaches to remyelination are now also being explored in clinical trials. Work continues to define intermediate outcomes that can provide results in phase 2 trials more quickly than disability measures, and more efficient trial designs, such as multi-arm multi-stage and futility approaches, are increasingly being used. Collaborations between patient organisations, pharmaceutical companies, and academic researchers will be crucial to ensure that future trials maintain this momentum and generate results that are relevant for people living with progressive multiple sclerosis.

摘要

尽管在复发型多发性硬化症的治疗中取得了成功,但对于许多多发性硬化症患者来说,进行性残疾仍在不断累积。如何中断进行性疾病背后的复杂病理过程仍然是一个令人生畏且持续存在的挑战。自 2014 年以来,已经批准了几种免疫调节方法来治疗进行性多发性硬化症,这些方法具有适度但具有临床意义的疗效,主要用于患有活动性炎症性疾病的患者。这些药物的批准需要进行大型的 3 期临床试验,以充分检测对残疾的有意义的影响。新类别的药物,如 Bruton 酪氨酸激酶抑制剂,即将结束临床试验阶段,几种候选神经保护化合物在 2 期临床试验中取得了成功,目前也正在临床试验中探索创新的髓鞘再生方法。工作仍在继续定义中间结果,以便在 2 期临床试验中比残疾测量更快地提供结果,并且越来越多地使用更有效的试验设计,如多臂多阶段和无效性方法。患者组织、制药公司和学术研究人员之间的合作对于确保未来的试验保持这种势头并为进行性多发性硬化症患者产生相关结果至关重要。

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