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Real‐world persistence of multiple sclerosis disease‐modifying therapies

Tallantyre, Emma C.; Dobson, Ruth; Froud, Joseph L. J.; St John, Frederika A.; Anderson, Valerie M.; Arun, Tarunya; Buckley, Lauren; Evangelou, Nikos; Ford, Helen L.; Galea, Ian; George, Sumi; Gray, Orla M.; Hibbert, Aimee M.; Hu, Mo; Hughes, Stella E.; Ingram, Gillian; Kalra, Seema; Lim, Chia‐Hui E.; Mathews, Joela T. M.; McDonnell, Gavin V.; Mescall, Naomi; Norris, Sam; Ramsay, Stephen J.; Rice, Claire M.; Russell, Melanie J.; Shawe‐Taylor, Marianne J.; Williams, Thomas E.; Harding, Katharine E.; Robertson, Neil P.

Authors

Emma C. Tallantyre

Ruth Dobson

Joseph L. J. Froud

Frederika A. St John

Valerie M. Anderson

Tarunya Arun

Lauren Buckley

Nikos Evangelou

Helen L. Ford

Ian Galea

Sumi George

Orla M. Gray

Aimee M. Hibbert

Mo Hu

Stella E. Hughes

Gillian Ingram

Seema Kalra

Chia‐Hui E. Lim

Joela T. M. Mathews

Gavin V. McDonnell

Naomi Mescall

Sam Norris

Stephen J. Ramsay

Claire M. Rice

Melanie J. Russell

Marianne J. Shawe‐Taylor

Thomas E. Williams

Katharine E. Harding

Neil P. Robertson



Abstract

Background and purpose: Treatment persistence is the continuation of therapy over time. It reflects a combination of treatment efficacy and tolerability. We aimed to describe real‐world rates of persistence on disease‐modifying therapies (DMTs) for people with multiple sclerosis (pwMS) and reasons for DMT discontinuation. Methods: Treatment data on 4366 consecutive people with relapse‐onset multiple sclerosis (MS) were pooled from 13 UK specialist centres during 2021. Inclusion criteria were exposure to at least one MS DMT and a complete history of DMT prescribing. PwMS in blinded clinical trials were excluded. Data collected included sex, age at MS onset, age at DMT initiation, DMT treatment dates, and reasons for stopping or switching DMT. For pwMS who had received immune reconstituting therapies (cladribine/alemtuzumab), discontinuation date was defined as starting an alternative DMT. Kaplan–Meier survival analyses were used to express DMT persistence. Results: In 6997 treatment events (1.6 per person with MS), median time spent on any single maintenance DMT was 4.3 years (95% confidence interval = 4.1–4.5 years). The commonest overall reasons for DMT discontinuation were adverse events (35.0%) and lack of efficacy (30.3%). After 10 years, 20% of people treated with alemtuzumab had received another subsequent DMT, compared to 82% of people treated with interferon or glatiramer acetate. Conclusions: Immune reconstituting DMTs may have the highest potential to offer a single treatment for relapsing MS. Comparative data on DMT persistence and reasons for discontinuation are valuable to inform treatment decisions and in personalizing treatment in MS.

Citation

Tallantyre, E. C., Dobson, R., Froud, J. L. J., St John, F. A., Anderson, V. M., Arun, T., …Robertson, N. P. (in press). Real‐world persistence of multiple sclerosis disease‐modifying therapies. European Journal of Neurology, Article e16289. https://doi.org/10.1111/ene.16289

Journal Article Type Article
Acceptance Date Mar 14, 2024
Online Publication Date Apr 3, 2024
Deposit Date Apr 8, 2024
Journal European Journal of Neurology
Print ISSN 1351-5101
Publisher Wiley
Peer Reviewed Peer Reviewed
Article Number e16289
DOI https://doi.org/10.1111/ene.16289
Keywords multiple sclerosis, treatment, persistence, disease‐modifying therapy


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