Evidence map›Paper›PMID 34433679›Full record

Trial reportNeurology2021

Comparison of the EDSS, Timed 25-Foot Walk, and the 9-Hole Peg Test as Clinical Trial Outcomes in Relapsing-Remitting Multiple Sclerosis.

Marcus W Koch, Jop P Mostert, Jerry S Wolinsky, Fred D Lublin, Bernard Uitdehaag, Gary R Cutter

Registry-linked trialOpen access · greenAbstract readClinical Trial, Phase IIIComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00211887 (A Multi-Center, Double-Blind, Randomized Study Comparing the Combined Use of Interferon Beta-1a and Glatiramer Acetate to Either Agent Alone in Patients With Relapsing-Remitting Multiple Sclerosis), which is not on this map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
3.6field-weighted citation impact, top 6% 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.

NCT00211887 phase3completednot on this map

A Multi-Center, Double-Blind, Randomized Study Comparing the Combined Use of Interferon Beta-1a and Glatiramer Acetate to Either Agent Alone in Patients With Relapsing-Remitting Multiple Sclerosis (CombiRx)

TypeinterventionalSponsorFred LublinRan2005 to 2013Enrolled1,008ConditionsRelapsing Remitting Multiple SclerosisArmsInterferon beta 1-a, glatiramer acetate, placebo
3 · Its place in the literature

Who cites it

29 citing papers in PubMed, 39 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Observational
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Brain hemodynamic responses and fall prediction in older adults with multiple sclerosis.Multiple sclerosis (Houndmills, Basingstoke, England) · 2024
    Article
  17. Depressive Symptoms in Multiple Sclerosis: Links to Body Composition, Physical Activity, and Functional Ability.Medical science monitor : international medical journal of experimental and clinical research · 2024
    Article
  18. Review
  19. Frontal-striatal tract integrity and depression in older adults with and without multiple sclerosis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
    Article
  20. Article
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

6 authors at 1 institution in 3 countries.

Marcus W KochFrom the Departments of Clinical Neurosciences (M.W.K.) and Community Health Sciences (M.W.K.), University of Calgary, Alberta, Canada; Department of Neurology (J.P.M.), Rijnstate Hospital, Arnhem, the Netherlands; Department of Neurology (J.S.W.), McGovern Medical School, University of Texas Health Science Center at Houston (UTHealth); Corinne Goldsmith Dickinson Center for MS (F.D.L.), Icahn School of Medicine at Mount Sinai, New York, NY; Department of Neurology (B.U.), MS Center Amsterdam, Amsterdam University Medical Centers, the Netherlands; and Department of Biostatistics (G.R.C.), University of Alabama at Birmingham. mwkoch@ucalgary.ca.
Jop P MostertFrom the Departments of Clinical Neurosciences (M.W.K.) and Community Health Sciences (M.W.K.), University of Calgary, Alberta, Canada; Department of Neurology (J.P.M.), Rijnstate Hospital, Arnhem, the Netherlands; Department of Neurology (J.S.W.), McGovern Medical School, University of Texas Health Science Center at Houston (UTHealth); Corinne Goldsmith Dickinson Center for MS (F.D.L.), Icahn School of Medicine at Mount Sinai, New York, NY; Department of Neurology (B.U.), MS Center Amsterdam, Amsterdam University Medical Centers, the Netherlands; and Department of Biostatistics (G.R.C.), University of Alabama at Birmingham.
Jerry S WolinskyFrom the Departments of Clinical Neurosciences (M.W.K.) and Community Health Sciences (M.W.K.), University of Calgary, Alberta, Canada; Department of Neurology (J.P.M.), Rijnstate Hospital, Arnhem, the Netherlands; Department of Neurology (J.S.W.), McGovern Medical School, University of Texas Health Science Center at Houston (UTHealth); Corinne Goldsmith Dickinson Center for MS (F.D.L.), Icahn School of Medicine at Mount Sinai, New York, NY; Department of Neurology (B.U.), MS Center Amsterdam, Amsterdam University Medical Centers, the Netherlands; and Department of Biostatistics (G.R.C.), University of Alabama at Birmingham.ORCID 0000-0002-8197-2762
Fred D LublinFrom the Departments of Clinical Neurosciences (M.W.K.) and Community Health Sciences (M.W.K.), University of Calgary, Alberta, Canada; Department of Neurology (J.P.M.), Rijnstate Hospital, Arnhem, the Netherlands; Department of Neurology (J.S.W.), McGovern Medical School, University of Texas Health Science Center at Houston (UTHealth); Corinne Goldsmith Dickinson Center for MS (F.D.L.), Icahn School of Medicine at Mount Sinai, New York, NY; Department of Neurology (B.U.), MS Center Amsterdam, Amsterdam University Medical Centers, the Netherlands; and Department of Biostatistics (G.R.C.), University of Alabama at Birmingham.
Bernard UitdehaagFrom the Departments of Clinical Neurosciences (M.W.K.) and Community Health Sciences (M.W.K.), University of Calgary, Alberta, Canada; Department of Neurology (J.P.M.), Rijnstate Hospital, Arnhem, the Netherlands; Department of Neurology (J.S.W.), McGovern Medical School, University of Texas Health Science Center at Houston (UTHealth); Corinne Goldsmith Dickinson Center for MS (F.D.L.), Icahn School of Medicine at Mount Sinai, New York, NY; Department of Neurology (B.U.), MS Center Amsterdam, Amsterdam University Medical Centers, the Netherlands; and Department of Biostatistics (G.R.C.), University of Alabama at Birmingham.
Gary R CutterFrom the Departments of Clinical Neurosciences (M.W.K.) and Community Health Sciences (M.W.K.), University of Calgary, Alberta, Canada; Department of Neurology (J.P.M.), Rijnstate Hospital, Arnhem, the Netherlands; Department of Neurology (J.S.W.), McGovern Medical School, University of Texas Health Science Center at Houston (UTHealth); Corinne Goldsmith Dickinson Center for MS (F.D.L.), Icahn School of Medicine at Mount Sinai, New York, NY; Department of Neurology (B.U.), MS Center Amsterdam, Amsterdam University Medical Centers, the Netherlands; and Department of Biostatistics (G.R.C.), University of Alabama at Birmingham.
University of Calgary · CA

Funding

Extension of Combination Therapy for Multiple Sclerosis (eCombiRx)U01NS045719 · NINDS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI LUBLIN, FRED D · 2003 to 2012
$44.7M
NINDS NIH HHS U01 NS045719
6 · The paper itself

Abstract

BACKGROUND AND

objectivesClinical trials in relapsing-remitting multiple sclerosis (RRMS) usually use the Expanded Disability Status Scale (EDSS) as their primary disability outcome measure, while the more recently developed outcomes timed 25-ft walk (T25FW) and 9-hole peg test (NHPT) may be more useful and patient relevant. The objective of this work was to compare the EDSS to the T25FW and NHPT in a large RRMS randomized controlled trial (RCT) dataset.

methodsWe used the dataset from Combination Therapy in Patients With Relapsing-Remitting Multiple Sclerosis (CombiRx) (clinicaltrials.gov identifier NCT00211887), a large phase 3 RCT, to compare the EDSS to the alternative outcomes T25FW and NHPT. We investigated disability worsening vs similarly defined improvement, unconfirmed vs confirmed and sustained disability change, and the presentation methods cumulative Kaplan-Meier survival curves vs cross-sectional disability worsening.

resultsCombiRx included 1,008 participants. A comparison of confirmed and sustained worsening events showed that, throughout the trial, there were substantially fewer sustained than confirmed events, with a positive predictive value of confirmed for sustained worsening at 24 months of 0.73 for the EDSS, 0.73 for the T25FW, and 0.8 for the NHPT. More concerning were the findings that worsening on the EDSS occurred as frequently as similarly defined improvement throughout the 3 years of follow-up and that improvement rates increased in parallel with worsening rates. The T25FW showed low improvement rates of <10% throughout the trial. We also found that Kaplan-Meier survival analysis, the standard presentation and analysis method in modern RRMS trials, yields exaggerated estimates of disability worsening. With the Kaplan-Meier method, the proportion of patients with worsening events steadily increases until it reaches several-fold the number of events seen with more conservative analysis methods. For 3-month confirmed disability worsening up to 36 months, the Kaplan-Meier method yields 2.6-fold higher estimates for the EDSS, 2.9-fold higher estimates for the T25FW, and 5.1-fold higher estimates for the NHPT compared to a more conservative presentation of the same data. DISCUSSION: Our analyses raise concerns about using the EDSS as the standard disability outcome in RRMS trials and suggest that the T25FW may be a more useful measure. These findings are relevant for the design and critical appraisal of RCTs.

Indexed as

Disability EvaluationTreatment OutcomeAdultDouble-Blind MethodDrug Therapy, CombinationFemaleGlatiramer AcetateHumansInterferon-betaMaleMiddle AgedMultiple Sclerosis, Relapsing-RemittingGlatiramer AcetateInterferon-beta

Identifiers

PMID34433679
PMCPMC9246083
OpenAlexW3193714945

What OpenQuestion holds

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Read underepoch 390

Registered trials

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.