Efficacy of tocilizumab in highly relapsing MOGAD with an inadequate response to intravenous immunoglobulin therapy: A case series
•MOGAD may exhibit high disease activity despite immunotherapies.•Relapses during IVIG treatment prompted the transition to tocilizumab.•All patients in this study achieved relapse-free after tocilizumab therapy.•Tocilizumab appears effective in MOGAD patients with poor response to IVIG. Myelin olig...
Saved in:
Published in | Multiple sclerosis and related disorders Vol. 91; p. 105859 |
---|---|
Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Netherlands
Elsevier B.V
01.11.2024
|
Subjects | |
Online Access | Get full text |
ISSN | 2211-0348 2211-0356 2211-0356 |
DOI | 10.1016/j.msard.2024.105859 |
Cover
Summary: | •MOGAD may exhibit high disease activity despite immunotherapies.•Relapses during IVIG treatment prompted the transition to tocilizumab.•All patients in this study achieved relapse-free after tocilizumab therapy.•Tocilizumab appears effective in MOGAD patients with poor response to IVIG.
Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) is an inflammatory disease affecting the central nervous system that may require long-term immunotherapy in relapsing cases. While immunotherapies utilized in neuromyelitis optica spectrum disorder have shown varying efficacy in MOGAD, intravenous immunoglobulin G (IVIG) recently emerged as a promising treatment. Tocilizumab, a monoclonal antibody that targets the interleukin-6 (IL-6) receptor, has been reported to be effective in refractory MOGAD in several case studies, where tocilizumab was introduced primarily due to rituximab failure.
This retrospective study was conducted in a single center and focused on MOGAD patients receiving tocilizumab therapy, who have shown limited response to various immunotherapies, including intravenous immunoglobulin G (IVIG) maintenance.
This study included four patients, three adults, and one child. They experienced a median of 9 attacks (range 6-9) throughout their disease course despite at least two immunotherapies. All patients transitioned to tocilizumab after experiencing a median of two relapses (range 1-3) while on IVIG maintenance for a median of 21.9 months (range 21.3-49.6 months). Following the monthly tocilizumab administration at a dose of 8g/kg, all patients remained relapse-free with a median follow-up duration of 25.0 months (range 9.8-51.3 months) without reported adverse events.
Targeting the IL-6 pathway appears to offer therapeutic benefits in highly relapsing MOGAD patients who poorly respond to IVIG maintenance therapy. |
---|---|
Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 ObjectType-Report-3 ObjectType-Case Study-4 |
ISSN: | 2211-0348 2211-0356 2211-0356 |
DOI: | 10.1016/j.msard.2024.105859 |