Progressive multiple sclerosis

被引:63
作者
Ontaneda, Daniel [1 ]
Fox, Robert J. [1 ]
机构
[1] Cleveland Clin, Lerner Coll Med, Mellen Ctr Multiple Sclerosis, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
clinical trials; multiple sclerosis; primary progressive; secondary progressive; DISABILITY STATUS SCALE; PLACEBO-CONTROLLED TRIAL; DOUBLE-BLIND; FUNCTIONAL COMPOSITE; INTERFERON BETA-1B; BRAIN ATROPHY; MS; MULTICENTER; EDSS; MRI;
D O I
10.1097/WCO.0000000000000195
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Purpose of reviewThe purpose of this study is to highlight the pathological features and clinical aspects of progressive multiple sclerosis (PMS) and also the results of clinical trial experience to date and review ongoing clinical trials and prospective new treatment options. This study will explain the challenges of clinical trial design in PMS.Recent findingsMultiple sclerosis (MS) has been identified as a chronic immune mediated disease, and the progressive phase of the disease appears to have significant neurodegenerative mechanisms. The classification of the course of PMS has been reorganized into categories of active vs. inactive inflammatory disease and the presence vs. absence of gradual disease progression. This differentiation allows clearer conceptualization of PMS and possibly even more efficient recruitment of PMS patients into clinical trials. Clinical trial experience to date in PMS has been negative with anti-inflammatory medications used in relapsing MS. Simvastatin was recently tested in a phase II trial and showed a 43% reduction of annualized atrophy progression in secondary progressive MS. Ongoing PMS trials are currently being conducted with the phosphodiesterase inhibitor ibudilast, S1P modulator siponimod and anti-B-cell therapy ocrelizumab. Several efforts for development of outcome measures in PMS are ongoing.SummaryPMS represents a significant challenge, as the pathogenesis of the disease is not well understood, no validated outcome metrics have been established and clinical trial experience to date has been disappointing. Advances in the understanding of the disease and lessons learned in previous clinical trials are paving the way for successful development of disease-modifying agents for this disease.
引用
收藏
页码:237 / 243
页数:7
相关论文
共 49 条
[11]   LOW-DOSE (7.5-MG) ORAL METHOTREXATE REDUCES THE RATE OF PROGRESSION IN CHRONIC PROGRESSIVE MULTIPLE-SCLEROSIS [J].
GOODKIN, DE ;
RUDICK, RA ;
MEDENDORP, SV ;
DAUGHTRY, MM ;
SCHWETZ, KM ;
FISCHER, J ;
VANDYKE, C .
ANNALS OF NEUROLOGY, 1995, 37 (01) :30-40
[12]   Rituximab in Patients with Primary Progressive Multiple Sclerosis Results of a Randomized Double-Blind Placebo-Controlled Multicenter Trial [J].
Hawker, Kathleen ;
O'Connor, Paul ;
Freedman, Mark S. ;
Calabresi, Peter A. ;
Antel, Jack ;
Simon, Jack ;
Hauser, Stephen ;
Waubant, Emmanuelle ;
Vollmer, Timothy ;
Panitch, Hillel ;
Zhang, Jiameng ;
Chin, Peter ;
Smith, Craig H. .
ANNALS OF NEUROLOGY, 2009, 66 (04) :460-471
[13]  
HUGHES RAC, 1988, LANCET, V2, P179
[14]   Lamotrigine for neuroprotection in secondary progressive multiple sclerosis: a randomised, double-blind, placebo-controlled, parallel-group trial [J].
Kapoor, Raju ;
Furby, Julian ;
Hayton, Thomas ;
Smith, Kenneth J. ;
Altmann, Daniel R. ;
Brenner, Robert ;
Chataway, Jeremy ;
Hughes, Richard A. C. ;
Miller, David H. .
LANCET NEUROLOGY, 2010, 9 (07) :681-688
[15]   Placebo-controlled multicentre randomised trial of interferon β-1b in treatment of secondary progressive multiple sclerosis [J].
Kappos, L ;
Polman, C ;
Pozzilli, C ;
Thompson, A ;
Dahlke, F ;
Knight, R ;
Hern, J ;
Coleman, R ;
Gerrie, L ;
Cooper, G ;
Moore, J ;
Boringa, J ;
van Oosten, B ;
Ronner, H ;
Schrijver, H ;
Truyen, L ;
Montalbán, J ;
Río, J ;
Tintoré, M ;
Jacas, C ;
Marzo, E ;
Lechner-Scott, J ;
Huber, S ;
Lienert, C ;
Brunnschweiler, H ;
Hawkins, S ;
Droogan, A ;
McDonnell, G ;
Duddy, M ;
McKinstry, S ;
Altenkirch, H ;
Baum, K ;
Einhäupl, K ;
Marx, P ;
Poewe, W ;
Walter, G ;
Akman, H ;
Brockmeier, B ;
Scherer, P ;
Zschenderlein, R ;
Schmierer, K ;
Gelderblom, H ;
Hartmann, A ;
Stapf, C ;
Lüschow, A ;
Mackert, B ;
Schumacher, H ;
Masuhr, F ;
Hempel, T ;
Zimmermann, R .
LANCET, 1998, 352 (9139) :1491-1497
[16]   Interferon beta-1b in secondary progressive MS - A combined analysis of the two trials [J].
Kappos, L ;
Weinshenker, B ;
Pozzilli, C ;
Thompson, AJ ;
Dahlke, F ;
Beckmann, K ;
Polman, C ;
McFarland, H .
NEUROLOGY, 2004, 63 (10) :1779-1787
[17]  
King J, 2001, NEUROLOGY, V56, P1496
[18]  
Koch MW, 2014, J NEUROL NEUROSURG P
[19]   Multiple sclerosis and chronic autoimmune encephalomyelitis -: A comparative quantitative study of axonal injury in active, inactive, and remyelinated lesions [J].
Kornek, B ;
Storch, MK ;
Weissert, R ;
Wallstroem, E ;
Stefferl, A ;
Olsson, T ;
Linington, C ;
Schmidbauer, M ;
Lassmann, H .
AMERICAN JOURNAL OF PATHOLOGY, 2000, 157 (01) :267-276
[20]   Responsiveness and predictive value of EDSS and MSFC in primary progressive MS [J].
Kragt, J. J. ;
Thompson, A. J. ;
Montalban, X. ;
Tintore, M. ;
Rio, J. ;
Polman, C. H. ;
Uitdehaag, B. M. J. .
NEUROLOGY, 2008, 70 (13) :1084-1091