The wearing-off phenomenon of ocrelizumab in patients with multiple sclerosis

A A Toorop1, Z Y G J van Lierop1, E M M Strijbis1

  • 1Department of Neurology, MS Center Amsterdam, Amsterdam University Medical Centers, Vrije Universiteit Amsterdam, Amsterdam Neuroscience, Neurology Outpatient Clinic, De Boelelaan 1118, 1081 HV, Amsterdam, the Netherlands.

Abstract

Insights

More than half of multiple sclerosis (MS) patients on ocrelizumab experience the wearing-off phenomenon, with higher BMI being a key predictor. This symptom does not indicate inadequate MS disease control.

Area of Science:

  • Neurology
  • Immunology
  • Pharmacology

Background:

  • Monoclonal antibody therapy for multiple sclerosis (MS) can lead to a wearing-off phenomenon, characterized by symptom exacerbation before the next dose.
  • Understanding the prevalence and predictors of this phenomenon is crucial for optimizing MS treatment.

Purpose of the Study:

  • To assess the prevalence of the wearing-off phenomenon in MS patients treated with ocrelizumab.
  • To identify factors that predict the occurrence of the wearing-off phenomenon.

Main Methods:

  • Prospective cohort study of 117 MS patients receiving ocrelizumab for over a year.
  • Data collected via questionnaires, including demographics, clinical/radiological data, CD19 B-cell counts, and serum neurofilament light (sNfL) levels.
  • Logistic regression analysis used to identify predicting factors.

Main Results:

  • 61% of patients reported the wearing-off phenomenon, most commonly fatigue, cognitive, and sensory symptoms.
  • Higher body mass index (BMI ≥ 25) was the only significant predictor (OR 2.70).
  • Infusion interval, EDSS, MRI activity, relapses, B-cell counts, and sNfL were not predictors.

Conclusions:

  • The wearing-off phenomenon affects over half of MS patients on ocrelizumab, with BMI as a sole predictor.
  • This phenomenon does not appear to be linked to extended infusion intervals or elevated B-cell counts.
  • Ocrelizumab's wearing-off phenomenon does not seem to indicate suboptimal control of MS disease activity.

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