Evidence map›Paper›PMID 41614472›Full record

ArticleEuropean stroke journal2026

Calibrated non-inferiority margin: a new pragmatic method to account for population shift in stroke trials.

Nuala Peter, Hannah Johns, Bruce C V Campbell, Bijoy Menon, Mark W Parsons, Leonid Churilov

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Article in European stroke journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Nuala PeterGlobal Biostatistics and Data Sciences, Boehringer Ingelheim Pharma GmbH and Co. KG, Biberach an der Riss, Germany.ORCID 0009-0004-5376-0238
Hannah JohnsMelbourne Medical School, University of Melbourne, Melbourne, Victoria, Australia.ORCID 0000-0003-2135-0504
Bruce C V CampbellDepartment of Medicine and Neurology, Melbourne Brain Centre, Royal Melbourne Hospital, University of Melbourne, Parkville, Victoria, Australia.ORCID 0000-0003-3632-9433
Bijoy MenonCalgary Stroke Program, University of Calgary Cumming School of Medicine, Calgary, Alberta, Canada.ORCID 0000-0002-3466-496X
Mark W ParsonsDepartment of Neurology, Liverpool Hospital, Liverpool, New South Wales, Australia.ORCID 0000-0001-8874-2487
Leonid ChurilovMelbourne Medical School, University of Melbourne, Melbourne, Victoria, Australia.ORCID 0000-0002-9807-6606

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionNon-inferiority trials in acute ischemic stroke (AIS) are crucial to improve access to high-quality care. Population shifts must be accounted for when estimating non-inferiority margins, eg, changes in population characteristics (trial vs historical data); however, existing methods have practical and statistical limitations. We propose a pragmatic conceptual approach and fully pre-specifiable procedure for calibrating non-inferiority margins that account for population shifts in observed trial populations. PATIENTS AND

methodsOur approach splits trial and historical data into subgroups based on relevant effect-modifying covariates. Trial data from TASTE, which investigated the effect (mRS score 0-1 at day 90) of tenecteplase vs alteplase, were compared to historical data from the Stroke Thrombolysis Trialists' Collaboration (STTC) meta-analysis (alteplase vs control). We reweighted the STTC treatment effect to match the shifted AIS population in TASTE before deriving the calibrated non-inferiority margin.

resultsFor both datasets, subgroups were based on onset-to-treatment time and baseline NIHSS values. The reweighted risk difference for alteplase vs control was 11.70% (95% CI, 6.67-16.73); the conservative treatment-effect estimate was 6.67%, corresponding to a risk difference of 3.33% (50% reduction). Hence, the calibrated margin for comparing alternative interventions to alteplase was set at -3.33%, consistent with the European Stroke Organisation's clinically recommended margin (-3.0%).

conclusionOur conceptual approach to estimate calibrated non-inferiority margins is a simple and pragmatic alternative to existing methods to account for population shifts in stroke trials. The supporting procedure has already been applied.

Indexed as

Fibrinolytic AgentsIschemic StrokeStrokeTissue Plasminogen ActivatorFemaleHumansFibrinolytic AgentsTissue Plasminogen Activatoradaptive trialsnon-inferioritypopulation shiftstatisticsstrokeSTTCTASTE

Identifiers

PMID41614472
PMCPMC12866653

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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.