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进展性多发性硬化症临床试验:经验教训。

Progressive MS trials: Lessons learned.

机构信息

The Queen Square Multiple Sclerosis Centre, Department of Neuroinflammation, UCL Institute of Neurology, University College London, London, UK/Department of Neurology-Neuroimmunology and Multiple Sclerosis Centre of Catalonia (Cemcat), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.

Department of Neurology-Neuroimmunology and Multiple Sclerosis Centre of Catalonia (Cemcat), Hospital Universitari Vall d'Hebron, Universitat Autònoma de Barcelona, Barcelona, Spain.

出版信息

Mult Scler. 2017 Oct;23(12):1583-1592. doi: 10.1177/1352458517729460.

Abstract

Up to very recently, no treatments had proved effective in progressive multiple sclerosis (MS). In 2016, four drugs, two tested in phase 3 and two in phase 2 trials, showed a beneficial effect in primary or secondary progressive MS. Although this could indicate a turning point in progressive MS treatment, most of these successes have been modest and mainly restricted to patients with active inflammation, in the context of trials with powerful anti-inflammatory agents. This paper summarises these reasons, particularly focusing on the main lessons learned for the design of future trials. First, a drug's mechanism of action should tackle the specific pathogenic mechanisms that characterise progressive MS. Second, trial populations where new drugs are to be tested should be carefully chosen, possibly including younger patients with shorter disease durations, which have greater chances of showing active deterioration during the trial, therefore increasing the power to detect treatment effects. Third, outcome measures used in future phase 2 and phase 3 trials should be highly sensitive and be accompanied by smart trial designs.

摘要

直到最近,还没有有效的治疗方法可以治疗进展性多发性硬化症(MS)。2016 年,有四种药物,两种在 3 期临床试验中进行了测试,两种在 2 期临床试验中进行了测试,显示出对原发性或继发性进展性 MS 有有益的影响。尽管这可能标志着进展性 MS 治疗的一个转折点,但这些成功大多是适度的,主要限于有活跃炎症的患者,在使用强力抗炎药物的试验中。本文总结了这些原因,特别是特别关注为未来试验设计而吸取的主要经验教训。首先,药物的作用机制应该针对进展性 MS 的特定致病机制。其次,要仔细选择将要测试新药的试验人群,可能包括年龄较小、疾病持续时间较短的患者,这些患者在试验期间更有可能出现明显恶化,从而提高检测治疗效果的能力。第三,未来 2 期和 3 期临床试验中使用的疗效指标应该高度敏感,并伴有明智的试验设计。

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