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Dimethyl fumarate vs Teriflunomide: an Italian time-to-event data analysis
Emanuele D'Amico1, Aurora Zanghì2, Mariangela Sciandra3
1Department "G.F. Ingrassia", MS Center University of Catania, Policlinico G. Rodolico, V. Santa Sofia 78, 95123, Catania, Italy. emanuele.damico@unict.it.
Dimethyl fumarate (DMF) and teriflunomide (TRF) are oral disease-modifying therapies for relapsing-remitting multiple sclerosis (RRMS). After 38 months, DMF showed a significantly lower risk of relapse compared to TRF, with similar control of MRI activity and disability progression.
Area of Science:
- Neurology
- Immunology
- Pharmacology
Background:
- Oral disease-modifying therapies (DMTs) have transformed the treatment landscape for relapsing-remitting multiple sclerosis (RRMS).
- Understanding the comparative effectiveness of different oral DMTs is crucial for optimizing patient care.
Purpose of the Study:
- To compare the real-world effectiveness of dimethyl fumarate (DMF) and teriflunomide (TRF) in a large, multicenter Italian cohort of RRMS patients.
- To evaluate treatment outcomes based on time-to-first-relapse, time-to-Magnetic Resonance Imaging (MRI)-activity, and time-to-disability-progression.
Main Methods:
- A retrospective analysis of 1445 RRMS patients treated with DMF or TRF between 2012 and 2018 across twelve Italian multiple sclerosis centers.
- Time-varying Cox-model analysis was employed to assess the primary outcomes, adjusting for baseline characteristics.
Main Results:
- Patients on TRF were older, predominantly male, and had a higher baseline disability level compared to those on DMF.
- While no significant difference in relapse risk was observed within the first 38 months, DMF demonstrated a significantly lower hazard of relapse beyond 38 months of therapy (HR=3.83, p=0.033).
- Both DMF and TRF showed comparable efficacy in controlling MRI activity and preventing disability progression.
Conclusions:
- Dimethyl fumarate (DMF) offers superior relapse-free survival compared to teriflunomide (TRF) for relapsing-remitting multiple sclerosis patients after 38 months of treatment.
- Both oral DMTs effectively manage disease activity and disability progression, but DMF may provide additional benefits in long-term relapse prevention.
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