Evidence map›Paper›PMID 25909083›Full record

ArticleAnnals of clinical and translational neurology2015

Comparative efficacy of switching to natalizumab in active multiple sclerosis.

Timothy Spelman, Tomas Kalincik, Annie Zhang, Fabio Pellegrini, Heinz Wiendl, Ludwig Kappos, Larisa Tsvetkova, Shibeshih Belachew, Robert Hyde, Freek Verheul and 12 more

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
8.2field-weighted citation impact, top 2% 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

27 citing papers in PubMed, 1 synthesis or guideline pooled it, 63 citations in OpenAlex.

  1. Pooled it
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  11. Early Aggressive Treatment Approaches for Multiple Sclerosis.Current treatment options in neurology · 2021
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  14. Observational
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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

22 authors at 16 institutions in 8 countries.

Timothy SpelmanDepartment of Medicine and Melbourne Brain Centre at the Royal Melbourne Hospital, University of Melbourne Melbourne, Australia.
Tomas KalincikDepartment of Medicine and Melbourne Brain Centre at the Royal Melbourne Hospital, University of Melbourne Melbourne, Australia.
Annie ZhangBiogen Idec Inc. Cambridge, Massachusetts.
Fabio PellegriniDepartment of Basic Medical Sciences, Neuroscience and Sense Organs, University of Bari Bari, Italy.
Heinz WiendlDepartment of Neurology, University of Münster Münster, Germany.
Ludwig KapposDepartment of Neurology, University Hospital Basel Basel, Switzerland.
Larisa TsvetkovaBiogen Idec Int BV Badhoevedorp, The Netherlands.
Shibeshih BelachewBiogen Idec Inc. Cambridge, Massachusetts.
Robert HydeBiogen Idec Inc. Cambridge, Massachusetts.
Freek VerheulGroene Hart Ziekenhuis Gouda, The Netherlands.
Francois Grand-MaisonNeuro Rive-Sud, Hôpital Charles LeMoyne Quebec, Canada.
Guillermo IzquierdoHospital Universitario Virgen Macarena Sevilla, Spain.
Pierre GrammondCenter de réadaptation déficience physique Chaudière-Appalache Levis, Canada.
Pierre DuquetteHôpital Notre Dame Montreal, Quebec, Canada.
Alessandra LugaresiMS Center, Department of Neuroscience, Imaging and Clinical Sciences, University "G. d'Annunzio" Chieti, Italy.
Jeannette Lechner-ScottJohn Hunter Hospital Newcastle, Australia.
Celia Oreja-GuevaraUniversity Hospital San Carlos Madrid, Spain.
Raymond HuppertsOrbis Medical Centre Sittard-Geleen, The Netherlands.
Thor PetersenKommunehospitalet Arhus C, Denmark.
Michael BarnettBrain and Mind Research Institute Sydney, Australia.
Maria TrojanoDepartment of Basic Medical Sciences, Neuroscience and Sense Organs, University of Bari Bari, Italy.
Helmut ButzkuevenDepartment of Medicine and Melbourne Brain Centre at the Royal Melbourne Hospital, University of Melbourne Melbourne, Australia ; Department of Neurology, Eastern Health, Monash University Box Hill, Australia.
Biogen (United States) · USUniversity of Bari Aldo Moro · ITBiogen (Netherlands) · NLEastern Health · AUGroene Hart Ziekenhuis · NLHôpital Charles-Le Moyne · CAHôpital Notre-Dame · CAHospital Clínico San Carlos · ESHospital Universitario Virgen Macarena · ESJohn Hunter Hospital · AUThe Royal Melbourne Hospital · AUUniversity Hospital of Basel · CHUniversity of Chieti-Pescara · ITUniversity of Melbourne · AUUniversity of Münster · DEZuyderland Medisch Centrum · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo compare treatment efficacy and persistence in patients who switched to natalizumab versus those who switched between glatiramer acetate (GA) and interferon-beta (IFNβ) after an on-treatment relapse on IFNβ or GA using propensity score matched real-world datasets.

methodsPatients included were registered in MSBase or the TYSABRI Observational Program (TOP), had relapsed on IFNβ or GA within 12 months prior to switching to another therapy, and had initiated natalizumab or IFNβ/GA treatment ≤6 months after discontinuing prior therapy. Covariates were balanced across post switch treatment groups by propensity score matching at treatment initiation. Relapse, persistence, and disability measures were compared between matched treatment arms in the total population (n = 869/group) and in subgroups defined by prior treatment history (IFNβ only [n = 578/group], GA only [n = 165/group], or both IFNβ and GA [n = 176/group]).

resultsCompared to switching between IFNβ and GA, switching to natalizumab reduced annualized relapse rate in year one by 65-75%, the risk of first relapse by 53-82% (mean follow-up 1.7-2.2 years) and treatment discontinuation events by 48-65% (all P ≤ 0.001). In the total population, switching to natalizumab reduced the risk of confirmed disability progression by 26% (P = 0.036) and decreased the total disability burden by 1.54 EDSS-years (P < 0.0001) over the first 24 months post switch.

interpretationUsing large, real-world, propensity-matched datasets we demonstrate that after a relapse on IFNβ or GA, switching to natalizumab (rather than between IFNβ and GA) led to superior outcomes for patients in all measures assessed. Results were consistent regardless of the prior treatment identity.

Identifiers

PMID25909083
PMCPMC4402083
OpenAlexW2077200500

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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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.