Escalating to medium- versus high-efficacy disease modifying therapy after low-efficacy treatment in relapsing remitting multiple sclerosis

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Jannis Müller - , University of Melbourne (Author)
  • Izanne Roos - , Royal Melbourne Hospital (Author)
  • Tomas Kalincik - , Royal Melbourne Hospital (Author)
  • Johannes Lorscheider - , University Hospital Basel (Author)
  • Edoardo Galli - , University Hospital Basel (Author)
  • Pascal Benkert - , University Hospital Basel (Author)
  • Sabine Schädelin - , University Hospital Basel (Author)
  • Sifat Sharmin - , Royal Melbourne Hospital (Author)
  • Maximilian Einsiedler - , University Hospital Basel (Author)
  • Peter Hänni - , Swiss Federation for Common Tasks of Health Insurances (SVK), Solothurn, Switzerland. (Author)
  • Jürg Schmid - , Swiss Federation for Common Tasks of Health Insurances (SVK), Solothurn, Switzerland. (Author)
  • Jens Kuhle - , University Hospital Basel (Author)
  • Tobias Derfuss - , University Hospital Basel (Author)
  • Cristina Granziera - , University Hospital Basel (Author)
  • Tjalf Ziemssen - , Department of Neurology, Dresden International University (DIU), University Hospital Carl Gustav Carus Dresden (Author)
  • Timo Siepmann - , Department of Neurology, Dresden International University (DIU), University Hospital Carl Gustav Carus Dresden (Author)
  • Özgür Yaldizli - , University Hospital Basel (Author)

Abstract

BACKGROUND: In patients with relapsing remitting multiple sclerosis (RRMS) on low-efficacy disease modifying therapies (DMT), the optimal strategy on how to escalate treatment once needed, remains unknown.

METHODS: We studied RRMS patients on low-efficacy DMTs listed in the Swiss National Treatment Registry, who underwent escalation to either medium- or high-efficacy DMTs. Propensity score-based matching was applied using 12 clinically relevant variables. Both groups were also separately matched with control subjects who did not escalate therapy. Time to relapse and to disability worsening were evaluated using Cox proportional hazard models.

RESULTS: Of 1037 eligible patients, we 1:1 matched 450 MS patients who switched from low-efficacy to medium-efficacy (n = 225; 76.0% females, aged 42.4 ± 9.9 years [mean ± SD], median EDSS 3.0 [IQR 2-4]) or high-efficacy DMTs (n = 225; 72.4% females, aged 42.2 ± 10.6 years, median EDSS 3.0 [IQR 2-4]). Escalation to high-efficacy DMTs was associated with lower hazards of relapses than medium-efficacy DMTs (HR = 0.67, 95% CI 0.47-0.95, p = .027) or control subjects (HR = 0.61, 95% CI 0.44-0.84, p = .003). By contrast, escalation from low to medium-efficacy DMTs did not alter the hazard for relapses when compared to controls (i.e. patients on low-efficacy DMT who did not escalate DMT during follow-up) CONCLUSION: Our nationwide registry analysis suggests that, once escalation from a low-efficacy DMT is indicated, switching directly to a high-efficacy treatment is superior to a stepwise escalation starting with a moderate-efficacy treatment.

Details

Original languageEnglish
Article numbere3498
Pages (from-to)e3498
JournalBrain and behavior
Volume14
Issue number5
Publication statusPublished - May 2024
Peer-reviewedYes

External IDs

PubMedCentral PMC11061202
Scopus 85191930538
ORCID /0000-0001-8799-8202/work/171553671

Keywords

Keywords

  • Humans, Multiple Sclerosis, Relapsing-Remitting/drug therapy, Female, Adult, Male, Middle Aged, Registries, Recurrence, Treatment Outcome, Switzerland