Evidence map›Paper›PMID 34816454›Full record

ArticleMuscle & nerve2022

Slowing the loss of physical function in amyotrophic lateral sclerosis with edaravone: Post hoc analysis of ALSFRS-R item scores in pivotal study MCI186-19.

Benjamin Rix Brooks, Erik P Pioro, Jonathan Katz, Fumihiro Takahashi, Koji Takei, Jeffrey Zhang, Stephen Apple

Open access · hybridAbstract read
In one paragraph

Article in Muscle & nerve, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 27% 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

7 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
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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

7 authors at 6 institutions in 2 countries.

Benjamin Rix BrooksAtrium Health Neurosciences Institute, Carolinas Medical Center, University of North Carolina School of Medicine - Charlotte Campus, North Carolina, USA.ORCID 0000-0002-1914-5061
Erik P PioroNeuromuscular Division, Davee Department of Neurology, Northwestern University, Feinberg School of Medicine, Chicago, Illinois, USA.ORCID 0000-0002-0737-6065
Jonathan KatzDepartment of Neurology, Forbes Norris MDA/ALS Center, California Pacific Medical Center, San Francisco, California, USA.
Fumihiro TakahashiMitsubishi Tanabe Pharma Corporation, Tokyo, Japan.
Koji TakeiMitsubishi Tanabe Pharma Corporation, Tokyo, Japan.
Jeffrey ZhangPrinceton Pharmatech, Princeton, New Jersey, USA.
Stephen AppleMitsubishi Tanabe Pharma America, Inc, Jersey City, New Jersey, USA.ORCID 0000-0002-3051-3953
Mitsubishi Group (Japan) · JPCalifornia Pacific Medical Center · USMitsubishi Corporation (United States) · USNeurosciences Institute · USNorthwestern University · USPrinceton University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPhase 3 study MCI186-19 demonstrated less loss of physical function with edaravone versus placebo, as measured by the revised Amyotrophic Lateral Sclerosis Functional Rating Scale (ALSFRS-R) total score. A 1-point drop in an individual ALSFRS-R item may be clinically meaningful. We assessed ALSFRS-R item score changes to identify clinical features protected by edaravone treatment.

methodsTime-to-event analysis was used to assess the cumulative probabilities of reductions in ALSFRS-R item scores and Amyotrophic Lateral Sclerosis Assessment Questionnaire (ALSAQ-40) subdomain scores.

resultsEdaravone use was accompanied by: (1) delayed drop of ≥1 point in ALSFRS-R item score for four items: salivation, walking, climbing stairs, orthopnea (unadjusted), or for two items: walking, climbing stairs (after Bonferroni correction for multiple comparisons); (2) delayed score transition from 4 or 3 at baseline to ≤2 for five items: swallowing, eating motion, walking, climbing stairs, orthopnea (unadjusted), or for one item: climbing stairs (after Bonferroni correction for multiple comparisons); and (3) delayed worsening of ALSAQ-40 domain scores representing daily living/independence, eating and drinking (unadjusted). DISCUSSION: These post-hoc analyses identified the ALSFRS-R item scores and ALSAQ-40 domain scores that were associated with preserved gross motor function and health-related quality of life, respectively, after edaravone treatment. Limitations of post-hoc analyses should be considered when interpreting these results. We recommend that clinical trials employing the ALSFRS-R include this type of analysis as a pre-specified secondary outcome measure.

Indexed as

Amyotrophic Lateral SclerosisDouble-Blind MethodEdaravoneHumansQuality of LifeSurveys and QuestionnairesEdaravoneALSFRS-R item scoresclinical trialsdisease progressionfunctional declinegross motor function

Identifiers

PMID34816454
PMCPMC9299623
OpenAlexW3216567520

What OpenQuestion holds

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LicenceCC BY-NC
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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.