从芬戈莫转为西泊尼莫治疗复发缓解型和继发性进行性多发性硬化症的益处和风险

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY Drugs in Research & Development Pub Date : 2023-12-01 Epub Date: 2023-08-28 DOI:10.1007/s40268-023-00434-6
Martin Vališ, Anat Achiron, Hans Peter Hartung, Jan Mareš, Veronika Tichá, Pavel Štourač, Simona Halusková, Francesco Angelucci, Zbyšek Pavelek
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引用次数: 0

摘要

多发性硬化症(MS)是一种影响中枢神经系统(CNS)的慢性神经退行性疾病。目前,多发性硬化症的治疗仅限于美国食品和药物管理局(FDA)和欧洲药品管理局(EMA)批准的几种通过免疫调节作用减缓疾病进展的药物。芬戈莫德和西波尼莫德具有相似的作用机制,因此,它们的治疗效果可能具有可比性。然而,尽管fingolimod主要用于复发缓解型多发性硬化症(RRMS),但根据EMA标签,西ponimod被推荐用于活动性继发性进展型多发性硬化症(SPMS)。临床医生和科学家正在分析患者是否可以从芬戈莫德转向西波尼莫德,并从治疗的角度确定这种转换的利弊。在这篇综述中,我们旨在讨论这两种药物的治疗效果,以及在最常见的多发性硬化症、RRMS和SPMS患者中,从芬戈莫德转向西泊尼莫的利弊。
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The Benefits and Risks of Switching from Fingolimod to Siponimod for the Treatment of Relapsing-Remitting and Secondary Progressive Multiple Sclerosis.

Multiple sclerosis (MS) is a chronic neurodegenerative disease that affects the central nervous system (CNS). Currently, MS treatment is limited to several Food and Drug Administration (FDA)- and European Medicines Agency (EMA)-approved medications that slow disease progression by immunomodulatory action. Fingolimod and siponimod have similar mechanisms of action, and consequently, their therapeutic effects may be comparable. However, while fingolimod is mainly used for relapsing-remitting MS (RRMS), siponimod, according to EMA label, is recommended for active secondary progressive MS (SPMS). Clinicians and scientists are analysing whether patients can switch from fingolimod to siponimod and identifying the advantages or disadvantages of such a switch from a therapeutic point of view. In this review, we aim to discuss the therapeutic effects of these two drugs and the advantages/disadvantages of switching treatment from fingolimod to siponimod in patients with the most common forms of MS, RRMS and SPMS.

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来源期刊
Drugs in Research & Development
Drugs in Research & Development Pharmacology, Toxicology and Pharmaceutics-Pharmacology
CiteScore
5.10
自引率
0.00%
发文量
31
审稿时长
8 weeks
期刊介绍: Drugs in R&D is an international, peer reviewed, open access, online only journal, and provides timely information from all phases of drug research and development that will inform clinical practice. Healthcare decision makers are thus provided with knowledge about the developing place of a drug in therapy. The Journal includes: Clinical research on new and established drugs; Preclinical research of direct relevance to clinical drug development; Short communications and case study reports that meet the above criteria will also be considered; Reviews may also be considered.
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