Evidence map›Paper›PMID 34383312›Full record

ArticleMuscle & nerve2021

Evaluating longitudinal therapy effects via the North Star Ambulatory Assessment.

Craig M McDonald, Lee-Jen Wei, Kevin M Flanigan, Gary Elfring, Panayiota Trifillis, Francesco Muntoni, ACT DMD Clinical Evaluator Training Group, ACT DMD Study Group

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Muscle & nerve, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01826487 (A Phase 3 Efficacy and Safety Study of Ataluren in Patients With Nonsense Mutation Dystrophinopathy), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.9field-weighted citation impact, top 28% 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.

NCT01826487 phase3completednot on this map

A Phase 3 Efficacy and Safety Study of Ataluren in Patients With Nonsense Mutation Dystrophinopathy

TypeinterventionalSponsorPTC TherapeuticsRan2013 to 2015Enrolled230ConditionsMuscular Dystrophy, Duchenne, Muscular Dystrophies, Muscular Disorders, Atrophic, Muscular DiseasesArmsAtaluren, Placebo
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Review
  5. 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

8 authors at 5 institutions in 2 countries.

Craig M McDonaldPhysical Medicine & Rehabilitation, University of California Davis, Davis, California, USA.
Lee-Jen WeiHarvard University, Boston, Massachusetts, USA.
Kevin M FlaniganNationwide Children's Hospital, Columbus, Ohio, USA.ORCID 0000-0001-6440-3376
Gary ElfringPTC Therapeutics Inc, South Plainfield, New Jersey, USA.
Panayiota TrifillisPTC Therapeutics Inc, South Plainfield, New Jersey, USA.
Francesco MuntoniUniversity College London Great Ormond Street Institute of Child Health and NIHR Biomedical Research Centre, London, UK.
ACT DMD Clinical Evaluator Training Group
ACT DMD Study Group
PTC Therapeutics (United States) · USGreat Ormond Street Hospital · GBHarvard University · USNationwide Children's Hospital · USUniversity of California, Davis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

INTRODUCTION/

aimsIn comparative studies, treatment effects are typically evaluated at a specific time point. When data are collected periodically, an alternative, clinically meaningful approach could be used to assess the totality of treatment effects. We applied a well-developed analytical procedure for evaluating longitudinal treatment effects using North Star Ambulatory Assessment (NSAA) data for illustration.

methodsThe NSAA comprises 17 scorable items/outcomes that measure changes in motor function. Using NSAA data from the published ataluren phase 3, randomized, placebo-controlled trial (NCT01826487), cumulative counts of failures to perform each item (transition from 2/1 [able/impaired] to 0 [unable]) were collected at specified time points for each patient over 48 wk. Treatment group-wise mean cumulative item failure count curves were constructed, comparing ataluren versus placebo and deflazacort versus prednisone/prednisolone among placebo-treated patients. The steeper the curve, the worse the outcome. A clinically meaningful summary of the between-group difference was provided for each comparison.

resultsThe curve was uniformly steeper for placebo than ataluren after 16 wk and for prednisone/prednisolone than deflazacort after 8 wk. The two curves in each comparison continued to diverge thereafter, indicating sustained treatment benefits over time. Using a unique analytical approach, cumulative failure rates were reduced, on average, by 27% for ataluren versus placebo (rate ratio, 0.73; 95% confidence interval [CI], 0.55-0.97; p = .027) and 28% for deflazacort versus prednisone/prednisolone (rate ratio, 0.72; 95% CI, 0.53-0.96; p = .028). DISCUSSION: Unlike fixed-time analyses, this analytical approach enabled demonstration of cumulative, longitudinal treatment effects over time using repeatedly measured NSAA observations.

Indexed as

Muscular Dystrophy, DuchenneClinical Trials, Phase III as TopicHumansPrednisolonePrednisoneRandomized Controlled Trials as TopicTreatment FailurePrednisolonePrednisoneDuchenne muscular dystrophyefficacymotor functionoutcome measuretreatment

Identifiers

PMID34383312
PMCPMC9290940
OpenAlexW3188033198

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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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.