Evidence map›Paper›PMID 27405225›Full record

ArticleBMC neurology2016

Design of TRUST, a non-interventional, multicenter, 3-year prospective study investigating an integrated patient management approach in patients with relapsing-remitting multiple sclerosis treated with natalizumab.

Tjalf Ziemssen, Achim Gass, Jens Wuerfel, Antonios Bayas, Björn Tackenberg, Volker Limmroth, Ralf Linker, Mathias Mäurer, Judith Haas, Martin Stangel and 3 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in BMC neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 12 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 11 institutions in 2 countries.

Tjalf ZiemssenDepartment of Neurology, MS Center Dresden, Center of Clinical Neuroscience, University Hospital Carl Gustav Carus, Dresden University of Technology, Fetscherstr. 74, 01307, Dresden, Germany. Tjalf.Ziemssen@uniklinikum-dresden.de.ORCID http://orcid.org/0000-0001-8799-8202
Achim GassDepartment of Neurology, University Medicine Mannheim UMM, University of Heidelberg, Mannheim, Germany.
Jens WuerfelMedical Image Analysis Center (MIAC AG), Basel, Switzerland.
Antonios BayasDepartment of Neurology, Hospital Augsburg, Augsburg, Germany.
Björn TackenbergDepartment of Neurology, Philipps University and University Clinics Gießen and Marburg, Marburg, Germany.
Volker LimmrothDepartment of Neurology, Cologne General Hospitals, University of Cologne, Cologne, Germany.
Ralf LinkerDepartment of Neurology, Friedrich-Alexander University Erlangen, Erlangen, Germany.
Mathias MäurerDepartment of Neurology, Caritas Hospital Bad Mergentheim, Bad Mergentheim, Germany.
Judith HaasDepartment of Neurology, Jewish Hospital, Berlin, Germany.
Martin StangelDepartment of Neurology, Clinical Neuroimmunology and Neurochemistry, Hannover Medical School, Hannover, Germany.
Matthias MeergansBiogen, Zug, Switzerland.
Olof HarlinBiogen, Ismaning, Germany.
Hans-Peter HartungDepartment of Neurology and Center for Neuropsychiatry, Medical Faculty, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany.
Biogen (Germany) · DEBiogen (Switzerland) · CHCaritas-Krankenhaus Bad Mergentheim · DEFriedrich-Alexander-Universität Erlangen-Nürnberg · DEHeidelberg University · DEHeinrich Heine University Düsseldorf · DEMedizinische Hochschule Hannover · DEUniversitätsklinikum Gießen und Marburg · DEUniversity Hospital Augsburg · DEUniversity Hospital Carl Gustav Carus · DEUniversity of Cologne · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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. DISCUSSION: TRUST 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.

Indexed as

Clinical ProtocolsDisease ManagementAntibodies, Monoclonal, HumanizedFemaleHumansLeukoencephalopathy, Progressive MultifocalMagnetic Resonance ImagingMaleMultiple Sclerosis, Relapsing-RemittingNatalizumabProspective StudiesRisk AssessmentAntibodies, Monoclonal, HumanizedNatalizumabJohn Cunningham virusNatalizumabProgressive multifocal leukoencephalopathyRelapsing-remitting multiple sclerosis

Identifiers

PMID27405225
PMCPMC4942949
OpenAlexW2470661728

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.