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继发进展型多发性硬化症的药物治疗:概述。

Pharmacotherapy in Secondary Progressive Multiple Sclerosis: An Overview.

机构信息

Queen Square Multiple Sclerosis Centre, Department of Neuroinflammation, UCL Institute of Neurology, Faculty of Brain Sciences, UCL, London, UK.

出版信息

CNS Drugs. 2018 Jun;32(6):499-526. doi: 10.1007/s40263-018-0538-0.

Abstract

Multiple sclerosis is an immune-mediated inflammatory disease of the central nervous system characterised by demyelination, neuroaxonal loss and a heterogeneous clinical course. Multiple sclerosis presents with different phenotypes, most commonly a relapsing-remitting course and, less frequently, a progressive accumulation of disability from disease onset (primary progressive multiple sclerosis). The majority of people with relapsing-remitting multiple sclerosis, after a variable time, switch to a stage characterised by gradual neurological worsening known as secondary progressive multiple sclerosis. We have a limited understanding of the mechanisms underlying multiple sclerosis, and it is believed that multiple genetic, environmental and endogenous factors are elements driving inflammation and ultimately neurodegeneration. Axonal loss and grey matter damage have been regarded as amongst the leading causes of irreversible neurological disability in the progressive stages. There are over a dozen disease-modifying therapies currently licenced for relapsing-remitting multiple sclerosis, but none of these has provided evidence of effectiveness in secondary progressive multiple sclerosis. Recently, there has been some early modest success with siponimod in secondary progressive multiple sclerosis and ocrelizumab in primary progressive multiple sclerosis. Finding treatments to delay or prevent the courses of secondary progressive multiple sclerosis is an unmet and essential goal of the research in multiple sclerosis. In this review, we discuss new findings regarding drugs with immunomodulatory, neuroprotective or regenerative properties and possible treatment strategies for secondary progressive multiple sclerosis. We examine the field broadly to include trials where participants have progressive or relapsing phenotypes. We summarise the most relevant results from newer investigations from phase II and III randomised controlled trials over the past decade, with particular attention to the last 5 years.

摘要

多发性硬化症是一种中枢神经系统的免疫介导的炎症性疾病,其特征是脱髓鞘、神经轴突丢失和异质性临床病程。多发性硬化症表现出不同的表型,最常见的是复发缓解型病程,较少见的是从疾病发作开始逐渐累积残疾的进展型(原发性进展性多发性硬化症)。大多数复发缓解型多发性硬化症患者在经过一段时间后,会转变为以逐渐神经恶化为特征的阶段,称为继发进展性多发性硬化症。我们对多发性硬化症的发病机制的了解有限,据信多种遗传、环境和内源性因素是驱动炎症并最终导致神经退行性变的因素。轴突丢失和灰质损伤被认为是进展期不可逆性神经功能障碍的主要原因之一。目前有十几种疾病修正治疗药物被许可用于治疗复发缓解型多发性硬化症,但没有一种药物在继发进展型多发性硬化症中证明有效。最近,西尼莫德在继发进展型多发性硬化症和奥瑞珠单抗在原发性进展型多发性硬化症中取得了一些早期适度的成功。寻找能够延缓或预防继发进展型多发性硬化症病程的治疗方法是多发性硬化症研究中的一个未满足的基本目标。在这篇综述中,我们讨论了具有免疫调节、神经保护或再生特性的药物的新发现以及继发进展型多发性硬化症的可能治疗策略。我们广泛考察了包括具有进展或复发表型的参与者的试验。我们总结了过去十年中来自 II 期和 III 期随机对照试验的较新调查的最相关结果,特别关注过去 5 年的结果。

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