Early high-efficacy treatment significantly reduces long-term disability in children with multiple sclerosis, new study finds

(Press-News.org) New research presented today at ECTRIMS 2024 reveals that initiating monoclonal antibody therapy during childhood, rather than delaying treatment until early adulthood, significantly reduces long-term disability in multiple sclerosis (MS) patients.1

The study, which utilised data from the French MS Registry, Italian MS Register, and the global MSBase Registry, analysed the outcomes of 282 patients with paediatric-onset MS who began experiencing symptoms before the age of 18 years. Patients were divided into two groups based on when they initiated monoclonal antibody treatment: either between the ages of 12-17 or 20-22 years.

To ensure comparability between the groups, the researchers used inverse probability treatment weighting based on propensity scores, which accounted for baseline differences in factors such as sex, age at symptom onset, time from onset to clinically definite MS, and the number of relapses. This approach enabled a clear assessment of how the timing of initiating high-efficacy therapy affects disability outcomes from ages 23 and over.

Using the Expanded Disability Status Scale (EDSS) to measure and monitor disability progression in MS, the study showed that patients who began treatment between the ages of 12-17 years (39% of the study group) had a mean absolute increase of only 0.40 points on the EDSS, compared to a 0.95-point increase in those who started treatment later (61% of the study group).

Between the ages of 23 and 27, the increase in EDSS scores from baseline was 0.57 points lower in the early treatment group compared to the late treatment group. The benefits of early treatment persisted throughout the median follow-up period of 10.8 years.  Dr Sifat Sharmin, research fellow in the Clinical Outcomes Research (CORe) Unit at the University of Melbourne and leader of the study states, “The substantially lower risk of progressing to higher disability levels in the early treatment group was particularly evident in the moderate disability range, where further progression was reduced by up to 97%.”

“This study highlights the critical importance of early intervention in paediatric-onset MS,” emphasises Dr. Sharmin. “Our findings indicate that initiating high-efficacy therapies like ocrelizumab, rituximab, or natalizumab during childhood can lead to significantly improved long-term outcomes, preserving neurological function and reducing disability progression.”

Currently, regulatory restrictions, due to limited evidence of the efficacy, safety, and impact of monoclonal antibodies on children's development, often delay access to these treatments for paediatric-onset MS patients until adulthood.2 “These findings are a strong argument for rethinking current treatment guidelines,” Dr. Sharmin urges. “By allowing earlier access to effective treatments, we can significantly enhance the quality of life for children with MS and reduce the burden of long-term disability.”

Looking ahead, the research team are dedicated to generating further evidence to support the proactive treatment of paediatric-onset MS, with a particular focus on assessing the long-term risks of immunosuppressive therapies in this population.

ENDS

 

Notes to Editors

A reference to ECTRIMS 2024 must be included in all coverage and/or articles associated with this study.

For more information or to arrange an expert interview, please contact the ECTRIMS Press Office at: press.ectrims@congrex.com

About the study author:

Dr Sifat Sharmin is a statistician and MS Australia postdoctoral research fellow in the Clinical Outcomes Research (CORe) Unit at the University of Melbourne, specialising in the analysis of large-scale longitudinal data from routine clinical practice. Her research focuses on bridging statistical advances with clinical decision-making in MS, investigating the prognostics and the effectiveness of available therapies to improve patient care. She has numerous MS publications, including many examining the effectiveness of different therapies.

About the European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS):

ECTRIMS is a non-profit organisation and an independent representative European-wide organisation devoted to MS. It serves as Europe’s and the world’s largest professional organisation dedicated to the understanding and treatment of MS.

The 40th ECTRIMS Congress takes place between 18-20 September 2024 in Copenhagen, Denmark.

Website: https://ectrims.eu/

References:

Long-term disability outcomes among children with multiple sclerosis treated with high-efficacy therapy, Sharmin, S. et al. (2024). Presented at ECTRIMS 2024. Mavridi, A., Bompou, M.E., Redmond, A. et al. (2024). Current and Emerging Treatment Options in Pediatric Onset Multiple Sclerosis. Sclerosis; 2(2):88-107. https://doi.org/10.3390/sclerosis2020007 END