Department of Clinical Neurosciences, University of Calgary, Calgary, AB, Canada.
Department of Community Health Sciences, University of Calgary, Calgary, AB, Canada.
Eur J Neurol. 2021 Jun;28(6):2115-2120. doi: 10.1111/ene.14732. Epub 2021 Jan 24.
It is unclear which cognitive outcome measure is the most useful for clinical trials in multiple sclerosis. To investigate the usefulness of the Symbol Digit Modalities Test (SDMT) as a clinical outcome measure in secondary progressive multiple sclerosis (SPMS), we describe the frequency of worsening and improvement events in a large randomized controlled trial (RCT) dataset.
Using original trial data from the ASCEND trial (n = 889), a recent large RCT in SPMS, we describe worsening and similarly defined improvement with and without 3-month confirmation on the SDMT in the whole trial cohort and unconfirmed worsening and improvement on the Paced Auditory Serial Addition Test (PASAT) in a smaller subset (n = 107).
Somewhat unexpectedly, SDMT scores steadily increased throughout the 2 years of follow-up in this trial. There were overall few SDMT worsening events throughout the trial (generally fewer than 10% of participants), but improvement events steadily increased from around 50% of participants with improvement at 12 weeks to more than 70% at 84 weeks and beyond. PASAT scores followed a similar pattern.
In this well-characterized clinical trial cohort, the SDMT does not reflect the steady cognitive decline that patients with SPMS experience. Both SDMT and PASAT scores improve throughout follow-up, possibly due to a practice effect. The SDMT may not be a useful outcome measure of disease progression in 2-year clinical trials in SPMS.
在多发性硬化症的临床试验中,哪种认知结果测量最有用尚不清楚。为了研究符号数字模态测验(SDMT)作为继发进展型多发性硬化症(SPMS)的临床结局测量指标的有用性,我们在一项大型随机对照试验(RCT)数据集描述了恶化和改善事件的频率。
使用 ASCEND 试验(n=889)的原始试验数据,这是一项针对 SPMS 的大型近期 RCT,我们描述了在整个试验队列中使用 SDMT 进行的未经 3 个月确认的恶化和类似定义的改善,以及在较小子集(n=107)中未经确认的 Paced Auditory Serial Addition Test(PASAT)恶化和改善。
出乎意料的是,在该试验的 2 年随访过程中,SDMT 分数稳步上升。整个试验中,SDMT 恶化事件总体较少(通常少于 10%的参与者),但改善事件稳步增加,从 12 周时约 50%的参与者改善,到 84 周及以后超过 70%。PASAT 分数也呈现出类似的模式。
在这个特征明确的临床试验队列中,SDMT 并不能反映 SPMS 患者经历的稳定认知下降。SDMT 和 PASAT 分数在整个随访过程中都有所提高,这可能是由于练习效应。SDMT 可能不是 SPMS 2 年临床试验中疾病进展的有用结局测量指标。