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