Abstract
Prolonged treatment with anti-CD20 antibodies can lead to hypogammaglobulinemia and increased infection risk in multiple sclerosis (MS). We investigated switch from anti-CD20 to cladribine as a strategy to prevent immunoglobulin reduction while preserving efficacy. We prospectively analysed serum IgG, IgM, neurofilament light (NfL) and glial fibrillary acidic protein (GFAP) in 44 patients, 14 who were switched from anti-CD20 to cladribine and 30 continuing anti-CD20. Over 1 year, serum IgG, IgM, NfL and GFAP remained stable after switch and similar to patients continuing anti-CD20. More than 90 % of patients remained free of disease activity. Cladribine should be further explored as de-escalating agent from anti-CD20 in MS.
Keywords:
Anti-CD20; Cladribine; De-escalation; Immunoglobulins; Neurofilaments.
Copyright © 2024. Published by Elsevier B.V.
MeSH terms
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Adult
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Antigens, CD20 / immunology
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Cladribine* / administration & dosage
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Cladribine* / pharmacology
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Drug Substitution
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Female
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Glial Fibrillary Acidic Protein / blood
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Humans
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Immunoglobulin G / blood
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Immunoglobulin M / blood
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Immunologic Factors / administration & dosage
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Immunologic Factors / pharmacology
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Immunosuppressive Agents / administration & dosage
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Male
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Middle Aged
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Multiple Sclerosis / blood
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Multiple Sclerosis / drug therapy
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Multiple Sclerosis / immunology
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Multiple Sclerosis, Relapsing-Remitting / blood
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Multiple Sclerosis, Relapsing-Remitting / drug therapy
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Neurofilament Proteins / blood
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Pilot Projects
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Prospective Studies
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Rituximab / administration & dosage
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Rituximab / pharmacology
Substances
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Cladribine
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neurofilament protein L
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Immunologic Factors
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Glial Fibrillary Acidic Protein
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Neurofilament Proteins
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Immunoglobulin G
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Immunoglobulin M
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Rituximab
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GFAP protein, human
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Immunosuppressive Agents
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Antigens, CD20