Evidence map›Paper›PMID 36131595›Full record

Trial reportMultiple sclerosis (Houndmills, Basingstoke, England)2022

Overall Disability Response Score: An integrated endpoint to assess disability improvement and worsening over time in patients with multiple sclerosis.

Ih Chang, Ludwig Kappos, Gavin Giovannoni, Peter A Calabresi, Alfred Sandrock, Wenting Cheng, Shan Xiao, Katherine Riester, Shibeshih Belachew, Aaron Deykin and 1 more

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Multiple sclerosis (Houndmills, Basingstoke, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

4 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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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

11 authors at 7 institutions in 3 countries.

Ih ChangCerevel Therapeutics, Cambridge, MA, USA.
Ludwig KapposResearch Center for Clinical Neuroimmunology and Neuroscience Basel (RC2NB), Departments of Head, Spine and Neuromedicine, Clinical Research, Biomedicine and Biomedical Engineering, University Hospital Basel, University of Basel, Basel, Switzerland.ORCID 0000-0003-4175-5509
Gavin GiovannoniBarts and The London School of Medicine and Dentistry, Queen Mary University, London, UK.
Peter A CalabresiThe Johns Hopkins Multiple Sclerosis Center, Baltimore, MD, USA.ORCID 0000-0002-7776-6472
Alfred SandrockVoyager Therapeutics, Cambridge, MA, USA.
Wenting ChengBiogen, Cambridge, MA, USA.
Shan XiaoTakeda Pharmaceuticals, Lexington, MA, USA.
Katherine RiesterBiogen, Cambridge, MA, USA.
Shibeshih BelachewBiogen, Cambridge, MA, USA.
Aaron DeykinUpstream Bio, Waltham, MA, USA.
Bing ZhuBiogen, Cambridge, MA, USA.ORCID 0000-0002-3975-4366
Biogen (United States) · USCerevel Therapeutics (United States) · USMultiple Sclerosis Center of Atlanta · USQueen Mary University of London · GBTakeda (United States) · USUniversity of Basel · CHVoyager Therapeutics (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOverall Disability Response Score (ODRS) is a composite endpoint including Expanded Disability Status Scale, Timed 25-foot Walk, and 9-Hole Peg Test, designed to quantify both disability improvement and worsening in multiple sclerosis (MS).

objectiveTo assess the sensitivity and clinical meaningfulness of ODRS using natalizumab Phase 3 data sets (AFFIRM in relapsing-remitting MS and ASCEND in secondary progressive MS).

methodsDifferences in ODRS over 96 weeks, ODRS at Week 96, and slope of ODRS change per year between natalizumab and placebo groups were analyzed. Correlation between ODRS and changes in patient-reported outcomes was also analyzed.

resultsThe difference (95% confidence interval (CI)) in the ODRS over 96 weeks between natalizumab and placebo groups was 0.34 (0.21-0.46) in AFFIRM (

conclusionThis analysis supports ODRS as a sensitive and potentially clinically meaningful disability outcome measure in MS.

Indexed as

Multiple SclerosisMultiple Sclerosis, Chronic ProgressiveMultiple Sclerosis, Relapsing-RemittingDisability EvaluationHumansNatalizumabWalkingNatalizumabdisability improvementdisability progressionDisability worseningmulticomponent outcome measureODRSrelapsing-remitting multiple sclerosissecondary progressive multiple sclerosis

Identifiers

PMID36131595
PMCPMC9732786
OpenAlexW4296623167

What OpenQuestion holds

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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.