Key result
Scheduled antibody testing significantly increased the proportion of multiple sclerosis patients who had a change in interferon-β therapy compared to usual care (19.6% vs 14.0%, p=0.004).
Why the study?
Does scheduled antibody testing alter therapy management in patients with multiple sclerosis on high-dose interferon-β?
RCT (n=1,358)
Open-label
1:1 assignment ratio stratified by center
Yes
Does scheduled antibody testing alter therapy management in patients with multiple sclerosis on high-dose interferon-β?
Providing clinicians with scheduled antibody test results significantly increased the rate of therapy changes in multiple sclerosis patients on high-dose interferon-beta.
Scheduled antibody testing increases interferon-β therapy changes in MS; supports routine monitoring to guide management decisions.
BACKGROUND: Many patients with relapsing-remitting multiple sclerosis (MS) treated with high-dose interferon-β (IFNβ) develop serum binding antibodies (BAb) and neutralizing antibodies (NAb). NAb reduces the biological activity of IFNβ, which contributes to clinical failure in these patients. We investigated whether access to antibody (Ab) test results would alter usual care of (IFNβ)-treated patients and whether BAb could predict NAb. METHODS: This was a randomized, controlled, open-label, parallel-group, multicenter study in patients with multiple sclerosis. Subjects (n = 1358) were randomly assigned to Ab testing or usual care. BAb and NAb titres were measured using standard assays. Primary and secondary outcomes were the proportion of patients whose IFNβ therapy changed and the type of and reasons for therapy changes. RESULTS: Therapy changes differed between the Ab testing and usual care arms (19.6% and 14.0%, respectively; p = 0 · 004). Results from Ab testing were more frequently reported as the reason for therapy change in the Ab testing arm than in the usual care arm (p < 0.0001). NAb and BAb positivity significantly increased the likelihood of therapy change and reduced IFNβ-associated adverse events. BAb titres were a significant predictor of NAb positivity (p = 0.0012). Initial BAb-positive and NAb-positive status in both study arms had a significant impact on the overall number of patients with a therapy change (p < 0.05). CONCLUSION: Access to Ab test results impacted therapy management. BAb titres can predict NAb positivity in patients on high-dose IFNβ.
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Fox et al. (2014) conducted an RCT in Multiple sclerosis (n=1,358). Scheduled antibody testing vs. Usual care was evaluated on Proportion of patients whose IFN β therapy changed (p=0.004). Scheduled antibody testing significantly increased the proportion of multiple sclerosis patients who had a change in interferon-β therapy compared to usual care (19.6% vs 14.0%, p=0.004).
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