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脊髓萎缩作为进展性多发性硬化症 II 期临床试验的主要结果指标。

Spinal cord atrophy as a primary outcome measure in phase II trials of progressive multiple sclerosis.

机构信息

Queen Square MS Centre, Department of Neuroinflammation, UCL Institute of Neurology, University College London (UCL), London, UK.

Queen Square MS Centre, Department of Neuroinflammation, UCL Institute of Neurology, University College London (UCL), London, UK/Translational Imaging Group, Centre for Medical Image Computing (CMIC), Department of Medical Physics and Biomedical Engineering, University College London (UCL), London, UK.

出版信息

Mult Scler. 2018 Jun;24(7):932-941. doi: 10.1177/1352458517709954. Epub 2017 May 18.

Abstract

OBJECTIVES

To measure the development of spinal cord (SC) atrophy over 1 year in patients with progressive multiple sclerosis (PMS) and determine the sample sizes required to demonstrate a reduction in spinal cord cross-sectional area (SC-CSA) as an outcome measure in clinical trials.

METHODS

In total, 44 PMS patients (26 primary progressive multiple sclerosis (PPMS), 18 secondary progressive multiple sclerosis (SPMS)) and 29 healthy controls (HCs) were studied at baseline and 12 months. SC-CSA was measured using the three-dimensional (3D) fast field echo sequences acquired at 3T and the active surface model. Multiple linear regressions were used to investigate changes in imaging measurements.

RESULTS

PPMS patients had shorter disease duration, lower Expanded Disability Status Scale (EDSS) and larger SC-CSA than SPMS patients. All patients together showed a significantly greater decrease in percentage SC-CSA change than HCs, which was driven by the PPMS. All patients deteriorated over 1 year, but no association was found between percentage SC-CSA change and clinical changes. The sample size per arm required to detect a 50% treatment effect over 1 year, at 80% power, was 57 for PPMS and 546 for SPMS.

CONCLUSION

SC-CSA may become an outcome measure in trials of PPMS patients, when they are at an early stage of the disease, have moderate disability and modest SC atrophy.

摘要

目的

测量进展型多发性硬化症(PMS)患者在 1 年内脊髓(SC)萎缩的发展情况,并确定在临床试验中作为结果测量来证明脊髓横截面积(SC-CSA)减少所需的样本量。

方法

共纳入 44 名 PMS 患者(26 名原发性进行性多发性硬化症(PPMS),18 名继发性进行性多发性硬化症(SPMS))和 29 名健康对照者(HCs),分别在基线和 12 个月时进行研究。使用 3T 获得的三维(3D)快速回波序列和主动表面模型来测量 SC-CSA。使用多元线性回归来研究影像学测量的变化。

结果

PPMS 患者的疾病持续时间较短,扩展残疾状况量表(EDSS)评分较低,SC-CSA 较大。所有患者的 SC-CSA 百分比变化的下降幅度明显大于 HCs,这主要是由 PPMS 患者引起的。所有患者在 1 年内都恶化了,但 SC-CSA 百分比变化与临床变化之间没有关联。在 1 年内,为了在 80%的效能下检测出 50%的治疗效果,每个手臂需要的样本量为 57 名 PPMS 患者和 546 名 SPMS 患者。

结论

当 PPMS 患者处于疾病早期、残疾程度中度且 SC 萎缩程度适中时,SC-CSA 可能成为临床试验的结果测量指标。

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