https://doi.org/10.55788/8a5b49e0
EAFToS is a 2-part study conducted in 8 Australian clinics. It links data from the digital support platform MSGo to other real-world data sources. Part II explores the impact of ofatumumab on relevant patient-reported outcomes (PROs) via data linkage between MSGo, MSBase, and centrally reviewed MRI findings. The primary endpoint was adherence, defined as the proportion of doses taken within 3 days of the expected date during initiation and the first 3 months of maintenance. Dr Anneke van der Walt (Monash University, Australia) presented the results [1]. The interim results from part I were also presented at ACTRIMS 2025 [2].
The interim analysis of part II of the EAFToS study included 100 patients. The mean EDSS score at baseline was 1.45; the mean time since diagnosis was 6.8 years. Most patients (60%) had received prior therapy, usually ocrelizumab. Of 92 patients, 89 adhered to initiation doses 2 and 3 (proportion 0.967). Adherence to maintenance doses 2 and 3 administered within 28 days was perfect (proportion 1.000). Of 100 patients, 3 discontinued treatment within 12 months (proportion 0.030).
Patients remained satisfied with their treatment over 6 months. The Treatment Satisfaction Questionnaire for Medication scores at 6 months versus baseline were:
- global satisfaction, 68.52 versus 72.37;
- effectiveness, 67.44 versus 70.18;
- side effects, 78.78 versus 82.80; and
- convenience, 87.92 versus 87.15.
Work Productivity and Activity Impairment Questionnaire scores were also positively affected. Absenteeism improved from 11.63 at baseline to 9.21 after 6 months. Presenteeism, work productivity lost, and activity impairment also improved. EQ5D and fatigue scores remained stable.
- Van Der Walt A, et al. Real-world use of ofatumumab in relapsing MS: Interim analysis of patient-reported and clinical outcomes from the EAFToS II study. V422, ACTRIMS 2025, 27 February–01 March 2025, West Palm Beach, FL, USA.
- Hardy T, et al. Characterizing ofatumumab patient onboarding and utilization in relapsing multiple sclerosis using MSGo: 3rd interim analysis of part I of the EAFToS study. P420, ACTRIMS 2025, 27 February–01 March 2025, West Palm Beach, FL, USA.
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Table of Contents: ACTRIMS 2025
Featured articles
Atypical and radiological-only presentations often meet 2024 MS criteria
Meet the Trialist: Dr Jiwon Oh
Safety Studies
Comorbidity burden associated with risk of adverse events
Update on safety profile of cladribine tablets yields positive results
Safety of 30-minute ublituximab infusions confirmed
NMOSD/MOGAD
Meningococcal vaccination prior to ravulizumab use seems effective
More Highlights
Orelabrutinib highly effective in relapsing-remitting MS, based on MRI results
Immunomodulatory potential of ketogenic diet in MS confirmed
A pre-relapse immune signature implicates EBV reactivation in MS relapse
Prediction and Prognosis
Genetic and phenotypic risk model predicts MS
Novel AI algorithm better identifies risk factors of MS
Paramagnetic rim lesions predict effectiveness of tolebrutinib
Imaging
Atypical and radiological-only presentations often meet 2024 MS criteria
Real-world Effectiveness
Treatment with cladribine tablets: real-world insights
Favourable effectiveness and persistence of cladribine versus other oral DMTs
Ofatumumab: good initial adherence and treatment satisfaction
MS activity remains low on long-term fenebrutinib
Higher-dosed ocrelizumab associated with less disability accrual
Ocrelizumab significantly reduces new/enlarging cortical lesions
Discontinuing therapy has few risks in patients with MS over 60 years
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