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

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

Affiliations
Review

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

Patricia K Coyle et al. Ann Clin Transl Neurol. 2024 Apr.

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.

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Conflict of interest statement

PKC has consulted for Accordant, Biogen, Bristol Myers Squibb, Eli Lilly and Company, Genentech, GlaxoSmithKline, Horizon Therapeutics, LabCorp, Mylan, Novartis, Sanofi/Genzyme, and TG Therapeutics; and has received research support from Actelion, Alkermes, Celgene, CorEvitas, Genentech/Roche, Janssen Pharmaceuticals, MedDay, NINDS, Novartis, and Sanofi/Genzyme. MSF has received research or educational grants from Sanofi/Genzyme Canada; received honoraria or consultation fees from Alexion/Astra Zeneca, Biogen Idec, EMD Inc/EMD Serono/Merck Serono, F. Hoffmann‐La Roche, Find Therapeutics, Novartis, Quanterix, Sanofi/Genzyme, and Teva Canada Innovation; is a member of a company advisory board, board of directors or other similar group of Actelion/Janssen (J&J), Alexion/Astra Zeneca, Atara Biotherapeutics, Bayer Healthcare, Celestra Health, EMD Inc./Merck Serono, F. Hoffmann‐La Roche, Find Therapeutics, Novartis, Sanofi/Genzyme, and Setpoint Medical; has participated in a company sponsored speaker's bureau for Sanofi/Genzyme and EMD Serono. BAC has received personal compensation from Mylan for consulting, and from Applied Clinical Intelligence for serving as an external adjudicator for a clinical trial conducted by Sanofi. BACC reports personal compensation for consulting for Alexion, Atara, Autobahn, Avotres, Biogen, Boston Pharma, EMD Serono, Gossamer Bio, Hexal/Sandoz, Horizon, Immunic AG, Kyverna, Neuron23, Novartis, Sanofi, and TG Therapeutics and research support from Genentech. CEM has consulted for Alexion, ANI, Banner Life Sciences, Biogen, Bristol Myers Squibb, EMD Serono, Genentech/Roche, Sanofi/Genzyme, Horizon Therapeutics, Immunic AG, Janssen/Actelion, Novartis, and TG Therapeutics.

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