Abstract

BackgroundNatalizumab provides rapid and high-efficacy control of multiple sclerosis disease activity with long-term stabilization. However, the benefits of the drug are countered by a risk of developing progressive multifocal leukoencephalopathy in patients infected with the John Cunningham Virus. Close monitoring is required in patients with increased progressive multifocal leukoencephalopathy risk receiving natalizumab in the long-term for an optimal benefit-risk evaluation. Standardized high-quality monitoring procedures may provide a superior basis for individual benefit and risk evaluation and thus improve treatment decisions. The non-interventional study TRUST was designed to capture natalizumab effectiveness under real-life conditions and to examine alternate approaches for clinical assessments, magnetic resonance imaging monitoring and use of biomarkers for progressive multifocal leukoencephalopathy risk stratification.Methods/DesignTRUST is a non-interventional, multicenter, prospective cohort study conducted at approximately 200 German neurological centers. The study is intended to enroll 1260 relapsing-remitting multiple sclerosis patients with ongoing natalizumab therapy for at least 12 months. Patients will be followed for a period of 3 years, irrespective of treatment changes after study start. Data on clinical, subclinical and patient-centric outcomes will be documented in order to compare the effectiveness of continuous versus discontinued natalizumab treatment. Furthermore, the type and frequency of clinical, magnetic resonance imaging and biomarker assessments, reasons for continuation or discontinuation of therapy and the safety profile of natalizumab will be collected to explore the impact of a systematic patient management approach and its potential impact on patient outcome. Specifically, the role of biomarkers, the use of expert opinions, the impact of high-frequency magnetic resonance imaging assessment for early progressive multifocal leukoencephalopathy detection and the role of additional radiological and clinical expert advice will be explored.DiscussionTRUST was initiated in spring 2014 and enrollment is anticipated to be completed by mid 2016. Annual interim analyses will deliver continuous information and transparency with regard to the patient cohorts and the completeness and quality of data as well as closely monitor any safety signals in the natalizumab-treated cohort. The study’s results may provide insights into opportunities to improve the benefit-risk assessment in clinical practice and support treatment decisions.

Highlights

  • Natalizumab provides rapid and high-efficacy control of multiple sclerosis disease activity with longterm stabilization

  • TRUST was initiated in spring 2014 and enrollment is anticipated to be completed by mid 2016

  • Here we report on the study design of the prospective, multicenter, non-interventional, long-term cohort study TRUST

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Summary

Discussion

We report on the study design of the prospective, multicenter, non-interventional, long-term cohort study TRUST. The study should improve the understanding of the use and discontinuation of natalizumab in the routine clinical practice setting, the influence of natalizumab on MS disease course, the effectiveness of sustained natalizumab treatment and the utility of risk-management and surveillance tools as well as expert opinions in the real-life setting. The utilization and the diagnostic and predictive value of risk stratification approaches (antiJCV antibody serostatus and index as well as additional non-validated biomarkers), as well as the use of MRI for the early detection of PML, have not been assessed to date in patients on long-term natalizumab treatment or in those switching to other MS therapies in routine clinical practice. The results of this study are expected to contribute to the improvement of MS patient management and to facilitate rational treatment decisions in patients receiving long-term therapy with natalizumab.

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Methods/Design
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