Zhang Yinan, Salter Amber, Wallström Erik, Cutter Gary, Stüve Olaf
Department of Neurology and Neurotherapeutics, the University of Texas Southwestern Medical Center, Dallas, TX, USA.
Division of Biostatistics, Washington University School of Medicine, St. Louis, MO, USA.
Ther Adv Neurol Disord. 2019 Feb 21;12:1756286419826547. doi: 10.1177/1756286419826547. eCollection 2019.
Clinical trials have advanced the treatment of multiple sclerosis (MS) by demonstrating the safety and efficacy of disease-modifying therapies (DMTs). This review discusses major changes to MS clinical trials in the era of DMTs. As treatment options for MS continue to increase, patients in modern MS trials present earlier and with milder disease compared with historic MS populations. While placebo-controlled trials for some questions may still be relevant, DMT trials in relapsing-remitting MS (RRMS) are no longer ethical. The replacement of the placebo arm by an active comparator arm in trials have raised the cost of trials by requiring larger sample sizes to detect on-study changes in treatment effects. Efforts to improve trial efficiency in RRMS have focused on exploring adaptive designs and relying on sensitive magnetic resonance imaging measures of disease activity. In trials for progressive forms of MS (PMS), the lack of sensitive outcome measures that can be used in shorter-term trials have delayed the development of effective treatments. Recent shifting of the focus to advancing trials in PMS has identified paraclinical outcome measurements with improved potential, and the testing of agents for neuroprotection and remyelination is in progress.
临床试验通过证明疾病修饰疗法(DMTs)的安全性和有效性,推动了多发性硬化症(MS)的治疗。本综述讨论了DMT时代MS临床试验的主要变化。随着MS治疗选择的不断增加,与历史上的MS患者群体相比,现代MS试验中的患者就诊时间更早,疾病症状也更轻。虽然对于某些问题,安慰剂对照试验可能仍然适用,但在复发缓解型MS(RRMS)中进行DMT试验已不符合伦理道德。在试验中用活性对照臂取代安慰剂臂,由于需要更大的样本量来检测治疗效果的研究内变化,增加了试验成本。提高RRMS试验效率的努力集中在探索适应性设计以及依赖疾病活动的敏感磁共振成像测量方法上。在进行性MS(PMS)试验中,缺乏可用于短期试验的敏感结局指标,延迟了有效治疗方法的开发。最近将重点转向推进PMS试验,已经确定了具有更大潜力的临床前结局测量方法,并且神经保护和髓鞘再生药物的试验正在进行中。