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

被引:36
作者
Cawley, Niamh [1 ]
Tur, Carmen [1 ]
Prados, Ferran [1 ,2 ]
Plantone, Domenico [1 ]
Kearney, Hugh [1 ]
Abdel-Aziz, Khaled [1 ]
Ourselin, Sebastian [2 ]
Wheeler-Kingshott, Claudia A. M. Gandini [1 ]
Miller, David H. [1 ,3 ]
Thompson, Alan J. [1 ,3 ]
Ciccarelli, Olga [1 ,3 ]
机构
[1] UCL, UCL Inst Neurol, Dept Neuroinflammat, Queen Sq MS Ctr, 1st Floor,Russell Sq House,10-12 Russell Sq, London WC1B 5EH, England
[2] UCL, Translat Imaging Grp, CMIC, Dept Med Phys & Biomed Engn, London, England
[3] UCL Hosp Biomed Res Ctr, London, England
关键词
Multiple sclerosis; spinal cord; progressive; magnetic resonance imaging; atrophy; CERVICAL CORD; DISABILITY; SEGMENTATION; MATTER; MRI; LESIONS; GREY;
D O I
10.1177/1352458517709954
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objectives: To measure the development of spinal cord (SC) atrophy over 1year 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 12months. 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 1year, 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 1year, 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.
引用
收藏
页码:932 / 941
页数:10
相关论文
共 28 条
[1]   Evidence for early neurodegeneration in the cervical cord of patients with primary progressive multiple sclerosis [J].
Abdel-Aziz, Khaled ;
Schneider, Torben ;
Solanky, Bhavana S. ;
Yiannakas, Marios C. ;
Altmann, Dan R. ;
Wheeler-Kingshott, Claudia A. M. ;
Peters, Amy L. ;
Day, Brian L. ;
Thompson, Alan J. ;
Ciccarelli, Olga .
BRAIN, 2015, 138 :1568-1582
[2]   The spinal cord in multiple sclerosis: Relationship of high-spatial-resolution quantitative MR imaging findings to histopathologic results [J].
Bot, JCJ ;
Blezer, ELA ;
Kamphorst, W ;
Nijeholt, GJLA ;
Ader, HJ ;
Castelijns, JA ;
Ig, KN ;
Bergers, E ;
Ravid, R ;
Polman, C ;
Barkhof, F .
RADIOLOGY, 2004, 233 (02) :531-540
[3]   Association of asymptomatic spinal cord lesions and atrophy with disability 5 years after a clinically isolated syndrome [J].
Brownlee, W. J. ;
Altmann, D. R. ;
Da Mota, P. Alves ;
Swanton, J. K. ;
Miszkiel, K. A. ;
Wheeler-Kingshott, C. A. M. Gandini ;
Ciccarelli, O. ;
Miller, D. H. .
MULTIPLE SCLEROSIS JOURNAL, 2017, 23 (05) :665-674
[4]   STEPS: Similarity and Truth Estimation for Propagated Segmentations and its application to hippocampal segmentation and brain parcelation [J].
Cardoso, M. Jorge ;
Leung, Kelvin ;
Modat, Marc ;
Keihaninejad, Shiva ;
Cash, David ;
Barnes, Josephine ;
Fox, Nick C. ;
Ourselin, Sebastien .
MEDICAL IMAGE ANALYSIS, 2013, 17 (06) :671-684
[5]   Reducing the Impact of White Matter Lesions on Automated Measures of Brain Gray and White Matter Volumes [J].
Chard, Declan T. ;
Jackson, Jonathan S. ;
Miller, David H. ;
Wheeler-Kingshott, Claudia A. M. .
JOURNAL OF MAGNETIC RESONANCE IMAGING, 2010, 32 (01) :223-228
[6]   Spinal cord repair in MS Does mitochondrial metabolism play a role? [J].
Ciccarelli, O. ;
Altmann, D. R. ;
McLean, M. A. ;
Wheeler-Kingshott, C. A. ;
Wimpey, K. ;
Miller, D. H. ;
Thompson, A. J. .
NEUROLOGY, 2010, 74 (09) :721-727
[7]   Development of a multiple sclerosis functional composite as a clinical trial outcome measure [J].
Cutter, GR ;
Baier, ML ;
Rudick, RA ;
Cookfair, DL ;
Fischer, JS ;
Petkau, J ;
Syndulko, K ;
Weinshenker, BG ;
Antel, JP ;
Confavreux, C ;
Ellison, GW ;
Lublin, F ;
Miller, AE ;
Rao, SM ;
Reingold, S ;
Thompson, A ;
Willoughby, E .
BRAIN, 1999, 122 :871-882
[8]   Assessing brain atrophy rates in a large population of untreated multiple sclerosis subtypes [J].
De Stefano, N. ;
Giorgio, A. ;
Battaglini, M. ;
Rovaris, M. ;
Sormani, M. P. ;
Barkhof, F. ;
Korteweg, T. ;
Enzinger, C. ;
Fazekas, F. ;
Calabrese, M. ;
Dinacci, D. ;
Tedeschi, G. ;
Gass, A. ;
Montalban, X. ;
Rovira, A. ;
Thompson, A. ;
Comi, G. ;
Miller, D. H. ;
Filippi, M. .
NEUROLOGY, 2010, 74 (23) :1868-1876
[9]   Pathological study of spinal cord atrophy in multiple sclerosis suggests limited role of local lesions [J].
Evangelou, N ;
DeLuca, GC ;
Owens, T ;
Esiri, MM .
BRAIN, 2005, 128 :29-34
[10]   The Multiple Sclerosis Functional Composite measure (MSFC): an integrated approach to MS clinical outcome assessment [J].
Fischer, JS ;
Rudick, RA ;
Cutter, GR ;
Reingold, SC .
MULTIPLE SCLEROSIS JOURNAL, 1999, 5 (04) :244-250