Early treatment delays long-term disability accrual in RRMS: Results from the BMSD network

Author:

Iaffaldano Pietro1ORCID,Lucisano Giuseppe2,Butzkueven Helmut3,Hillert Jan4,Hyde Robert5,Koch-Henriksen Nils6,Magyari Melinda6ORCID,Pellegrini Fabio5,Spelman Tim7ORCID,Sørensen Per Soelberg6,Vukusic Sandra8ORCID,Trojano Maria1

Affiliation:

1. Department of Basic Medical Sciences, Neurosciences and Sense Organs, University of Bari Aldo Moro, Bari, Italy

2. Department of Basic Medical Sciences, Neurosciences and Sense Organs, University of Bari Aldo Moro, Bari, Italy/Center for Outcomes Research and Clinical Epidemiology (CORESEARCH), Pescara, Italy

3. Department of Neurology, Box Hill Hospital, Monash University, Melbourne, VIC, Australia

4. Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden

5. Biogen International GmbH, Zug, Switzerland

6. Department of Neurology, The Danish Multiple Sclerosis Registry, Rigshospitalet, Copenhagen, Denmark

7. Department of Neurology, Box Hill Hospital, Monash University, Melbourne, VIC, Australia/Department of Clinical Neuroscience, Karolinska Institutet, Stockholm, Sweden

8. Neurology, Multiple Sclerosis, Myelin Disorders and Neuroinflammation, Pierre Wertheimer Neurological Hospital, Hospices Civils de Lyon, Lyon, France/Observatoire Français de la Sclérose en Plaques (OFSEP), Lyon, France

Abstract

Background: The optimal timing of treatment starts for achieving the best control on the long-term disability accumulation in multiple sclerosis (MS) is still to be defined. Objective: The aim of this study was to estimate the optimal time to start disease-modifying therapies (DMTs) to prevent the long-term disability accumulation in MS, using a pooled dataset from the Big Multiple Sclerosis Data (BMSD) network. Methods: Multivariable Cox regression models adjusted for the time to first treatment start from disease onset (in quintiles) were used. To mitigate the impact of potential biases, a set of pairwise propensity score (PS)-matched analyses were performed. The first quintile, including patients treated within 1.2 years from onset, was used as reference. Results: A cohort of 11,871 patients (median follow-up after treatment start: 13.2 years) was analyzed. A 3- and 12-month confirmed disability worsening event and irreversible Expanded Disability Status Scale (EDSS) 4.0 and 6.0 scores were reached by 7062 (59.5%), 4138 (34.9%), 3209 (31.1%), and 1909 (16.5%) patients, respectively. The risk of reaching all the disability outcomes was significantly lower ( p < 0.0004) for the first quintile patients’ group. Conclusion: Real-world data from the BMSD demonstrate that DMTs should be commenced within 1.2 years from the disease onset to reduce the risk of disability accumulation over the long term.

Funder

Biogen

Publisher

SAGE Publications

Subject

Neurology (clinical),Neurology

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