Treatment outcomes in multiple sclerosis using reduced and extended interval ocrelizumab dosing

Antonia McLean1, Simon Arnett1, Joshua Yap1

  • 1Department of Neurology, Gold Coast University Hospital, Southport QLD 4215, Australia.

Abstract

Insights

Reduced ocrelizumab dosing for multiple sclerosis (MS) patients showed similar clinical and radiological outcomes compared to standard dosing. This suggests modified ocrelizumab regimens are safe and effective for pwMS.

Area of Science:

  • Neurology
  • Immunology
  • Pharmacology

Background:

  • Ocrelizumab dosing was modified during the COVID-19 pandemic for people with multiple sclerosis (pwMS) due to infection risk and hospital access challenges.
  • Reduced dosing (RD) and extended interval dosing (EID) were implemented, deviating from standard dosing (SD).
  • The study aimed to compare the effectiveness and safety of these modified regimens against SD.

Purpose of the Study:

  • To evaluate the clinical and radiological outcomes of reduced ocrelizumab dosing (RD) and extended interval dosing (EID) in pwMS.
  • To assess the safety profile of modified ocrelizumab dosing strategies.
  • To compare these outcomes with standard dosing (SD) in a real-world setting.

Main Methods:

  • Retrospective data collection from 113 pwMS treated with ocrelizumab between 01/01/2018 and 01/01/2024.
  • Analysis of clinical relapse, MRI lesions, B cells, and immunoglobulin levels.
  • Calculation of annualized relapse risk and comparison across SD, RD, and EID groups.

Main Results:

  • No significant differences in clinical or radiological outcomes were observed between SD, RD, and EID regimens.
  • B-cell repopulation occurred more frequently with EID compared to SD.
  • A non-significant trend towards higher immunoglobulin levels was noted with RD and EID.

Conclusions:

  • Modified ocrelizumab dosing strategies (RD and EID) did not compromise clinical or radiological outcomes in pwMS.
  • These findings support the potential efficacy and safety of reduced ocrelizumab exposure.
  • Further prospective studies are warranted to explore these dosing strategies in MS management.

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