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1
Bioavailable central nervous system disease-modifying therapies for multiple sclerosis.多发性硬化症的中枢神经系统疾病修饰治疗的生物利用度。
Front Immunol. 2023 Nov 29;14:1290666. doi: 10.3389/fimmu.2023.1290666. eCollection 2023.
2
Narrative review based on fingolimod therapy in pediatric MS.基于芬戈莫德治疗儿童多发性硬化症的叙述性综述。
SAGE Open Med. 2023 May 8;11:20503121231171996. doi: 10.1177/20503121231171996. eCollection 2023.
3
An update on the use of sphingosine 1-phosphate receptor modulators for the treatment of relapsing multiple sclerosis.鞘氨醇 1-磷酸受体调节剂在治疗复发性多发性硬化症中的应用进展。
Expert Opin Pharmacother. 2023 Mar;24(4):495-509. doi: 10.1080/14656566.2023.2178898. Epub 2023 Mar 22.
4
The impact of sphingosine-1-phosphate receptor modulators on COVID-19 and SARS-CoV-2 vaccination.鞘氨醇-1-磷酸受体调节剂对 COVID-19 和 SARS-CoV-2 疫苗接种的影响。
Mult Scler Relat Disord. 2023 Jan;69:104425. doi: 10.1016/j.msard.2022.104425. Epub 2022 Nov 22.
5
S1P receptor modulators and the cardiovascular autonomic nervous system in multiple sclerosis: a narrative review.1-磷酸鞘氨醇受体调节剂与多发性硬化症中的心血管自主神经系统:一篇叙述性综述
Ther Adv Neurol Disord. 2022 Nov 22;15:17562864221133163. doi: 10.1177/17562864221133163. eCollection 2022.
6
Sphingosine-1 Phosphate Receptor Modulators: The Next Wave of Oral Therapies in Inflammatory Bowel Disease.鞘氨醇-1-磷酸受体调节剂:炎症性肠病口服治疗的新一波浪潮。
Gastroenterol Hepatol (N Y). 2022 May;18(5):265-271.
7
Sphingosine-1-Phosphate (S1P) and S1P Signaling Pathway Modulators, from Current Insights to Future Perspectives.鞘氨醇-1-磷酸(S1P)及其信号通路调节剂:从当前认识到未来展望。
Cells. 2022 Jun 29;11(13):2058. doi: 10.3390/cells11132058.
8
Long-term safety and efficacy of ozanimod in relapsing multiple sclerosis: Up to 5 years of follow-up in the DAYBREAK open-label extension trial.奥扎莫德治疗复发型多发性硬化症的长期安全性和疗效:DAYBREAK 开放性延伸试验长达 5 年的随访结果。
Mult Scler. 2022 Oct;28(12):1944-1962. doi: 10.1177/13524585221102584. Epub 2022 Jun 28.
9
Long-term Treatment With Ponesimod in Relapsing-Remitting Multiple Sclerosis: Results From Randomized Phase 2b Core and Extension Studies.在复发缓解型多发性硬化症中的长期用ponsimod 治疗:来自随机 2b 期核心和扩展研究的结果。
Neurology. 2022 Aug 23;99(8):e762-e774. doi: 10.1212/WNL.0000000000200606. Epub 2022 Jun 6.
10
COVID-19 Vaccination in Multiple Sclerosis and Inflammatory Diseases: Effects from Disease-Modifying Therapy, Long-Term Seroprevalence and Breakthrough Infections.多发性硬化症和炎症性疾病中的新冠病毒疫苗接种:疾病修正治疗的影响、长期血清阳性率和突破性感染
Vaccines (Basel). 2022 Apr 28;10(5):695. doi: 10.3390/vaccines10050695.

鞘氨醇 1-磷酸受体调节剂在多发性硬化症治疗中的应用:实践综述。

Sphingosine 1-phosphate receptor modulators in multiple sclerosis treatment: A practical review.

机构信息

Department of Neurology, Stony Brook Renaissance School of Medicine, Stony Brook University, Stony Brook, New York, USA.

University of Ottawa, Department of Medicine and the Ottawa Hospital Research Institute, Ottawa, Ontario, Canada.

出版信息

Ann Clin Transl Neurol. 2024 Apr;11(4):842-855. doi: 10.1002/acn3.52017. Epub 2024 Feb 16.

DOI:10.1002/acn3.52017
PMID:38366285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11021614/
Abstract

Four sphingosine 1-phosphate (S1P) receptor modulators (fingolimod, ozanimod, ponesimod, and siponimod) are approved by the US Food and Drug Administration for the treatment of multiple sclerosis. This review summarizes efficacy and safety data on these S1P receptor modulators, with an emphasis on similarities and differences. Efficacy data from the pivotal clinical trials are generally similar for the four agents. However, because no head-to-head clinical studies were conducted, direct efficacy comparisons cannot be made. Based on the adverse event profile of S1P receptor modulators, continued and regular monitoring of patients during treatment will be instructive. Notably, the authors recommend paying attention to the cardiac monitoring guidelines for these drugs, and when indicated screening for macular edema and cutaneous malignancies before starting treatment. To obtain the best outcome, clinicians should choose the drug based on disease type, history, and concomitant medications for each patient. Real-world data should help to determine whether there are meaningful differences in efficacy or side effects between these agents.

摘要

四种鞘氨醇 1-磷酸(S1P)受体调节剂(芬戈莫德、奥扎尼莫德、培尼莫德和西尼莫德)已获得美国食品和药物管理局批准用于治疗多发性硬化症。本综述总结了这些 S1P 受体调节剂的疗效和安全性数据,重点介绍了它们的相似之处和不同之处。四项关键性临床试验的疗效数据通常在这四种药物中是相似的。然而,由于没有进行头对头的临床研究,因此无法进行直接的疗效比较。基于 S1P 受体调节剂的不良事件谱,在治疗期间对患者进行持续和定期监测将具有指导意义。值得注意的是,作者建议关注这些药物的心脏监测指南,并在开始治疗前根据需要筛查黄斑水肿和皮肤恶性肿瘤。为了获得最佳结果,临床医生应根据疾病类型、病史和每位患者的伴随药物为其选择药物。真实世界的数据应有助于确定这些药物在疗效或副作用方面是否存在有意义的差异。