Evidence map›Paper›PMID 38730097›Full record

Trial reportJournal of neurology2024

Long-term clinical outcomes in patients with CIS treated with interferon beta-1b: results from the 15-year follow up of the BENEFIT trial.

Ludwig Kappos, Gilles Edan, Mark S Freedman, Hans-Peter Hartung, Xavier Montalbán, Frederik Barkhof, Ralf Koelbach, David G MacManus, Eva-Maria Wicklein, BENEFIT and BENEFIT 15 Study Groups

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Ludwig KapposResearch Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), Departments of Head-Organs, Spine and Neuromedicine, Clinical Research, Biomedicine and Biomedical Engineering, University Hospital and University of Basel, Spitalstrasse 2, 4031, Basel, Switzerland. Ludwig.Kappos@usb.ch.ORCID http://orcid.org/0000-0003-4175-5509
Gilles EdanCHU Hôpital Pontchaillou, Rennes, France.
Mark S FreedmanDepartment of Medicine, University of Ottawa and The Ottawa Hospital Research Institute, Ottawa, Canada.
Hans-Peter HartungDepartment of Neurology, Medical Faculty, Heinrich-Heine Universität, Düsseldorf, Germany.
Xavier MontalbánMultiple Sclerosis Center of Catalonia (Cemcat), Hospital Universitari Vall d'Hebron, Barcelona, Spain.
Frederik BarkhofAmsterdam UMC, Location Vrije Universiteit, Amsterdam, The Netherlands.
Ralf KoelbachIngress-Health HWM GmbH, Wismar, Germany.
David G MacManusUCL Queen Square Institute of Neurology, London, UK.
Eva-Maria WickleinBayer AG, Berlin, Germany.
BENEFIT and BENEFIT 15 Study Groups

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple sclerosis (MS) treatment intervention with immunomodulating therapy at early disease stage improves short term clinical outcomes. The objective of this study is to describe the long-term outcomes and healthcare utilization of patients with clinically isolated syndrome (CIS) included in the Betaferon®/Betaseron® in Newly Emerging MS for Initial Treatment (BENEFIT) randomized, parallel group trial. In BENEFIT patients were assigned to "early" IFNB-1b treatment or placebo ("delayed" treatment). After 2 years or conversion to clinically definite multiple sclerosis (CDMS), all patients were offered IFNB-1b and were reassessed 15 years later. Of 468 patients, 261 (55.8%) were enrolled into BENEFIT 15 (161 [55.1%] from the early, 100 [56.8%] from the delayed treatment arm). In the full BENEFIT analysis set, risk of conversion to CDMS remained lower in the early treatment group ( - 30.5%; hazard ratio 0.695 [95% CI, 0.547-0.883]; p = 0.0029) with a 15.7% lower risk of relapse than in the delayed treatment group (p = 0.1008). Overall, 25 patients (9.6%; 9.9% early, 9.0% delayed) converted to secondary progressive multiple sclerosis. Disability remained low and stable with no significant difference between groups in Expanded Disability Status Scale score or MRI metrics. Paced Auditory Serial Addition Task-3 scores were better in the early treatment group (p = 0.0036 for treatment effect over 15 years). 66.3% of patients were still employed at Year 15 versus 74.7% at baseline. In conclusion, results 15 years from initial randomization support long-term benefits of early treatment with IFNB-1b.

Indexed as

Interferon beta-1bMultiple SclerosisAdultDemyelinating DiseasesDisease ProgressionDouble-Blind MethodFemaleFollow-Up StudiesHumansMaleMiddle AgedTreatment OutcomeYoung AdultInterferon beta-1bClinically isolated syndromeImmunotherapyInterferon beta-1bMultiple sclerosis

Identifiers

PMID38730097
PMCPMC11233376

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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.