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Disease-modifying treatment preferences and decision-making in a multiple sclerosis randomized and observational clinical trial (DELIVER-MS)

  • Emma C. Tallantyre
  • , Sarah M. Planchon
  • , Harriet Howard
  • , John Mays
  • , Nadia Frowd
  • , Jeffrey A. Cohen
  • , Alasdair Coles
  • , Carrie M. Hersh
  • , Deborah M. Miller
  • , Meredith Dever
  • , Emma H. Gray
  • , Nicholas G. LaRocca
  • , Kunio Nakamura
  • , Clare Bale
  • , Gwen Covey-Crump
  • , Enrique Alvarez
  • , Tarunya Arun
  • , Wallace J. Brownlee
  • , Matt Craner
  • , Leorah Freeman
  • Natasha Frost, Myla D. Goldman, Rajesh K. Gupta, Katharine E. Harding, Jeremy Hobart, George J. Hutton, Megan H. Hyland, Seema Kalra, Meena Kannan, Orhun Kantarci, Daniel Lashley, Oliver Lily, Don Mahad, Jacqueline A. Nicholas, Richard Nicholas, David Paling, Owen R. Pearson, Claire M. Rice, Rohini Samudralwar, William F. Schmalstieg, Mini Singh, Ei Zune The, Bianca Weinstock-Guttman, Aram Zabeti, Thomas E. Love, Douglas D. Gunzler, Yi Liu, Stephen Gerry, Nikos Evangelou, Daniel Ontaneda
  • Cardiff University
  • Cardiff & Vale University Health Board
  • Mellen Ctr. for MS Treatm./Res.
  • Nottingham University Hospitals NHS Trust
  • University of Cambridge
  • Cleveland Clinic Foundation
  • MS Society
  • National MS Society
  • Nottingham
  • University of Bristol
  • Rocky Mountain MS Center
  • University of Warwick
  • Neurology Clinical Reference Group
  • University College London
  • University College London Hospitals NHS Foundation Trust
  • University of Oxford
  • Frimley Health NHS Foundation Trust
  • University of Texas at Austin
  • University of Wisconsin-Madison
  • Virginia Commonwealth University
  • University of Texas Health Science Center at Houston
  • Aneurin Bevan Health Board
  • University of Plymouth
  • Baylor College of Medicine
  • University of Rochester
  • University Hospitals of North Midlands NHS Trust
  • Keele University
  • Atlanta Neuroscience Institute
  • Mayo Clinic Rochester, MN
  • Leeds Teaching Hospitals NHS Trust
  • University of Edinburgh
  • Riverside Methodist Hospital
  • Imperial College Healthcare NHS Trust
  • Sheffield Teaching Hospitals NHS Foundation Trust
  • Swansea Bay University Health Board
  • North Bristol NHS Trust
  • University of Pennsylvania
  • University of Minnesota Twin Cities
  • University of Virginia
  • University Hospitals of Leicester NHS Trust
  • University of Cincinnati
  • Case Western Reserve University
  • University of Nottingham

Research output: Contribution to journalArticlepeer-review

Abstract

Background: There is growing support for high-efficacy disease-modifying therapy (DMT) in multiple sclerosis (MS), but escalation (ESC) approaches remain common. Objective: To describe decision-making in a pragmatic trial of early high-efficacy treatment (EHT) versus ESC. Methods: DELIVER-MS is a multi-center, pragmatic, randomized controlled trial (RCT) with a parallel observational study (OBS), which enrolled treatment-naïve people with RRMS in 31 UK/US sites. Primary outcome was as follows: 36-month brain volume loss according to initial treatment approach (EHT vs. ESC). Stepwise multivariable logistic regression was used to predict participation in RCT versus OBS and choice of EHT versus ESC within the OBS cohort. Results: In total, 816 people with MS were enrolled. Participants declined randomization due to preference for a particular DMT (85%), efficacy concerns (20%), and safety concerns (9%). RCT versus OBS participation was associated with lower relapse rate (p = 0.043) and greater brain parenchymal fraction (p = 0.002). Among 374 in the OBS cohort, 125 (33%) chose ESC and 249 (67%) chose EHT. People commencing EHT had higher education attainment (p < 0.001) and relapse rate (p = 0.025). Conclusion: Baseline DELIVER-MS data demonstrate that participants with milder disease are more likely to participate in RCT. The choice of EHT versus ESC was associated with demographic factors and disease activity. Clinical trial registration: NCT03535298.

Original languageEnglish
Pages (from-to)722-736
Number of pages15
JournalMultiple Sclerosis Journal
Volume32
Issue number7
DOIs
StatePublished - Jun 2026

Keywords

  • clinical trial
  • disease-modifying therapy
  • escalation
  • high efficacy
  • Multiple sclerosis

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