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Intravenous methylprednisolone as add-on induction therapy for chronic inflammatory demyelinating polyradiculoneuropathy: a randomised controlled trial

  • Sander R.M. Bus
  • , Iris N. van Doorn
  • , Laura Zambreanu
  • , On behalf of the OPTIC study group
  • , Luuk Wieske
  • , Johannes A. Bogaards
  • , Ahmed Abbas
  • , Yusuf A. Rajabally
  • , Alexander F.J.E. Vrancken
  • , Pieter A. van Doorn
  • , Robert D.M. Hadden
  • , Camiel Verhamme
  • , Rob J. de Haan
  • , Corianne A.J.M. de Borgie
  • , Ivo N. van Schaik
  • , Michael P. Lunn
  • , Filip Eftimov*
  • , Janneke G.J. Hoeijmakers
  • , Nicol Voermans
  • , Paul W. Wirtz
  • Mariëlle Padberg, Maarten de Rijk, Adája Baars, Govind Chavada, James Miller, James K.L. Holt, Stephen W. Reddel
*Corresponding author for this work
  • Amsterdam UMC
  • National Hospital for Neurology and Neurosurgery
  • University Hospitals Birmingham NHS Foundation Trust
  • Utrecht University
  • King’s College Hospital
  • Sanquin Blood Supply Foundation
  • University College London Hospitals NHS Foundation Trust

Research output: Contribution to journalArticleAcademicpeer-review

4 Citations (Scopus)
1 Downloads (Pure)

Abstract

Background: Most patients with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) require maintenance treatment. We aimed to determine whether combined treatment with intravenous immunoglobulin (IVIg) and intravenous methylprednisolone (IVMP) increases remission rates compared with IVIg and placebo. Methods: We performed a randomised, double-blind, placebo-controlled study. Adults with CIDP who were treatment naive, relapsed after a remission or required continued treatment after a single IVIg dose were included. Participants were treated with IVMP (1000 mg) or placebo (sodium chloride) every 3 weeks for 18 weeks. All participants received IVIg treatment consisting of a loading dose (2 g/kg) and serial maintenance treatments (1 g/kg). The primary outcome was remission, defined as sustained improvement on disability scales at 52 weeks without need for further treatment. Results: Enrolment was halted after the inclusion of 77 of the 96 planned participants because of safety concerns: four thromboembolic events occurred in the IVIg/IVMP group compared with none in the IVIg/placebo group. 14 of 37 (38%) participants in the IVIg/IVMP group were in remission at 52 weeks compared with 11 out of 40 (28%) in the IVIg/placebo group, with a difference of 10% (95% CI −11 to 31; p=0.47). Several secondary outcomes showed a greater magnitude of improvement in disability and impairment at 18 and 52 weeks in the IVIg/IVMP group. Conclusions: The study was prematurely stopped due to safety concerns after four thromboembolic events in the IVIg plus IVMP group. Combined treatment did not lead to significantly more frequent remissions than IVIg alone in the doses used in this study. Trial registration number: ISRCTN15893334.

Original languageEnglish
Pages (from-to)558-566
Number of pages9
JournalJournal of Neurology, Neurosurgery and Psychiatry
Volume97
Issue number6
DOIs
Publication statusPublished - Jun 2026

Bibliographical note

Publisher Copyright: © Author(s) (or their employer(s)) 2026.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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