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Updated: Jun 29, 2025

The Multiple Sclerosis Performance Test MSPT: An iPad-Based Disability Assessment Tool
Published on: June 30, 2014
Real-world persistence of multiple sclerosis disease-modifying therapies
Emma C Tallantyre1,2, Ruth Dobson3,4, Joseph L J Froud1,5
1Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK.
Treatment persistence for multiple sclerosis (MS) varies by therapy. Immune-reconstituting therapies like alemtuzumab show higher long-term persistence compared to older disease-modifying therapies (DMTs).
Area of Science:
- Neurology
- Immunology
- Pharmacology
Background:
- Treatment persistence is crucial for managing multiple sclerosis (MS), reflecting therapy efficacy and tolerability.
- Understanding real-world persistence and discontinuation reasons for disease-modifying therapies (DMTs) is vital for optimizing patient care.
Purpose of the Study:
- To determine real-world persistence rates of DMTs in people with MS (pwMS).
- To identify primary reasons for DMT discontinuation in pwMS.
- To compare persistence across different classes of MS DMTs.
Main Methods:
- Retrospective analysis of treatment data from 4366 pwMS across 13 UK centers (2021).
- Inclusion criteria: exposure to at least one MS DMT with a complete prescription history.
- Kaplan-Meier survival analysis used to assess DMT persistence; discontinuation defined by starting a new DMT for immune reconstituting therapies.
Main Results:
- Median time on a single maintenance DMT was 4.3 years.
- Most common discontinuation reasons: adverse events (35.0%) and lack of efficacy (30.3%).
- After 10 years, only 20% on alemtuzumab switched DMTs, versus 82% on interferon or glatiramer acetate.
Conclusions:
- Immune-reconstituting DMTs demonstrate potential for sustained treatment in relapsing MS.
- Comparative DMT persistence data aids in informed treatment decisions and personalized MS management.
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