Primary progressive multiple sclerosis: current therapeutic strategies and future perspectives

被引:18
作者
Gajofatto, Alberto [1 ]
Turatti, Marco [2 ]
Benedetti, Maria Donata [2 ]
机构
[1] Univ Verona, Dept Neurosci Biomed & Movement Sci, Verona, Italy
[2] Azienda Osped Univ Integrata Verona, Dept Neurosci, Verona, Italy
关键词
Multiple sclerosis; primary progressive; treatment; disease-modifying therapy; immunosuppressive drugs; immunomodulatory drugs; ocrelizumab; PLACEBO-CONTROLLED TRIAL; TOTAL LYMPHOID IRRADIATION; RECOMBINANT-HUMAN-ERYTHROPOIETIN; DOUBLE-BLIND; PHASE-III; INTERFERON BETA-1B; NATURAL-HISTORY; CONTROLLED MULTICENTER; GLATIRAMER ACETATE; EFFICACY ANALYSIS;
D O I
10.1080/14737175.2017.1257385
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Introduction: Multiple sclerosis (MS) is a chronic inflammatory condition of the central nervous system with heterogeneous features. Primary progressive (PP) MS is a rare disease subtype characterized by continuous disability worsening from onset. No disease-modifying therapy is currently approved for PP MS due to the negative or inconsistent results of clinical trials conducted on a wide range of interventions, which are reviewed in the present paper. Areas covered: The features and results of randomized trials of disease-modifying treatments for PP MS are discussed, including immunosuppressants, immunomodulators, monoclonal antibodies, and putative neuroprotective agents. Expert commentary: The recent encouraging results of the ocrelizumab trial in PP MS, the first to reach the primary disability endpoint, indicate B cells as a promising therapeutic target to prevent disease progression. Other emerging treatment strategies include cell metabolism modulation and inflammatory pathways inhibition, which are being investigated in several ongoing phase II and III placebocontrolled trials. Future PP MS trials will need to systematically include efficacy endpoints other than physical disability alone, such as cognition, quality of life, advanced MRI measures and molecular biomarkers.
引用
收藏
页码:393 / 406
页数:14
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