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Ofatumumab versus Teriflunomide in Multiple Sclerosis.奥法妥木单抗与特立氟胺治疗多发性硬化症的比较。
N Engl J Med. 2020 Aug 6;383(6):546-557. doi: 10.1056/NEJMoa1917246.
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Contribution of Relapse-Independent Progression vs Relapse-Associated Worsening to Overall Confirmed Disability Accumulation in Typical Relapsing Multiple Sclerosis in a Pooled Analysis of 2 Randomized Clinical Trials.在两项随机临床试验的汇总分析中,复发无关进展与复发相关恶化对典型复发型多发性硬化症总体确认残疾累积的贡献。
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Diroximel Fumarate Demonstrates an Improved Gastrointestinal Tolerability Profile Compared with Dimethyl Fumarate in Patients with Relapsing-Remitting Multiple Sclerosis: Results from the Randomized, Double-Blind, Phase III EVOLVE-MS-2 Study.在复发缓解型多发性硬化症患者中,与富马酸二甲酯相比,富马酸二罗西美显示出更好的胃肠道耐受性:随机、双盲、III期EVOLVE-MS-2研究结果。
CNS Drugs. 2020 Feb;34(2):185-196. doi: 10.1007/s40263-020-00700-0.
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B cells in autoimmune and neurodegenerative central nervous system diseases.自身免疫性和神经退行性中枢神经系统疾病中的 B 细胞。
Nat Rev Neurosci. 2019 Dec;20(12):728-745. doi: 10.1038/s41583-019-0233-2. Epub 2019 Nov 11.
5
Risk of natalizumab-associated PML in patients with MS is reduced with extended interval dosing.多发性硬化症患者使用延长间隔剂量可降低纳他珠单抗相关进行性多灶性脑白质病的风险。
Neurology. 2019 Oct 8;93(15):e1452-e1462. doi: 10.1212/WNL.0000000000008243. Epub 2019 Sep 12.
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Safety and efficacy of ozanimod versus interferon beta-1a in relapsing multiple sclerosis (RADIANCE): a multicentre, randomised, 24-month, phase 3 trial.奥扎莫德与干扰素β-1a 在复发型多发性硬化症(RADIANCE)中的安全性和疗效:一项多中心、随机、24 个月、3 期临床试验。
Lancet Neurol. 2019 Nov;18(11):1021-1033. doi: 10.1016/S1474-4422(19)30238-8. Epub 2019 Sep 3.
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Safety and efficacy of ozanimod versus interferon beta-1a in relapsing multiple sclerosis (SUNBEAM): a multicentre, randomised, minimum 12-month, phase 3 trial.奥扎莫德与干扰素β-1a 在复发型多发性硬化症中的安全性和疗效(SUNBEAM):一项多中心、随机、至少 12 个月、3 期临床试验。
Lancet Neurol. 2019 Nov;18(11):1009-1020. doi: 10.1016/S1474-4422(19)30239-X. Epub 2019 Sep 3.
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Silent progression in disease activity-free relapsing multiple sclerosis.疾病活动无复发缓解型多发性硬化的静息进展。
Ann Neurol. 2019 May;85(5):653-666. doi: 10.1002/ana.25463. Epub 2019 Mar 30.
9
Autologous Hematopoietic Cell Transplantation for Treatment-Refractory Relapsing Multiple Sclerosis: Position Statement from the American Society for Blood and Marrow Transplantation.自体造血细胞移植治疗难治性复发性多发性硬化症:美国血液和骨髓移植学会立场声明。
Biol Blood Marrow Transplant. 2019 May;25(5):845-854. doi: 10.1016/j.bbmt.2019.02.014. Epub 2019 Feb 19.
10
The prevalence of MS in the United States: A population-based estimate using health claims data.美国多发性硬化症的患病率:基于健康索赔数据的人群估计。
Neurology. 2019 Mar 5;92(10):e1029-e1040. doi: 10.1212/WNL.0000000000007035. Epub 2019 Feb 15.

多发性硬化症的治疗:综述

Treatment of Multiple Sclerosis: A Review.

作者信息

Hauser Stephen L, Cree Bruce A C

机构信息

UCSF Weill Institute for Neurosciences and Department of Neurology, University of California, San Francisco.

UCSF Weill Institute for Neurosciences and Department of Neurology, University of California, San Francisco.

出版信息

Am J Med. 2020 Dec;133(12):1380-1390.e2. doi: 10.1016/j.amjmed.2020.05.049. Epub 2020 Jul 17.

DOI:10.1016/j.amjmed.2020.05.049
PMID:32682869
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7704606/
Abstract

Multiple sclerosis (MS) is an autoimmune demyelinating and neurodegenerative disease of the central nervous system, and the leading cause of nontraumatic neurological disability in young adults. Effective management requires a multifaceted approach to control acute attacks, manage progressive worsening, and remediate bothersome or disabling symptoms associated with this illness. Remarkable advances in treatment of all forms of MS, and especially for relapsing disease, have favorably changed the long-term outlook for many patients. There also has been a conceptual shift in understanding the immune pathology of MS, away from a purely T-cell-mediated model to recognition that B cells have a key role in pathogenesis. The emergence of higher-efficacy drugs requiring less frequent administration have made these preferred options in terms of tolerability and adherence. Many experts now recommend use of these as first-line treatment for many patients with early disease, before permanent disability is evident.

摘要

多发性硬化症(MS)是一种中枢神经系统的自身免疫性脱髓鞘和神经退行性疾病,也是年轻成人非创伤性神经残疾的主要原因。有效的管理需要多方面的方法来控制急性发作、处理病情的进行性恶化,并缓解与该疾病相关的令人烦恼或致残的症状。各种形式的MS治疗,尤其是复发型疾病的治疗取得了显著进展,这对许多患者的长期预后产生了积极影响。在理解MS的免疫病理学方面也发生了概念上的转变,从单纯的T细胞介导模型转向认识到B细胞在发病机制中起关键作用。需要给药频率更低的高效药物的出现,使其在耐受性和依从性方面成为首选。现在许多专家建议,对于许多早期疾病患者,在永久性残疾明显之前,将这些药物用作一线治疗。