Evidence map›Paper›PMID 40491339›Full record

ArticleBiometrical journal. Biometrische Zeitschrift2025

Statistical Modeling to Adjust for Time Trends in Adaptive Platform Trials Utilizing Non-Concurrent Controls.

Pavla Krotka, Martin Posch, Mohamed Gewily, Günter Höglinger, Marta Bofill Roig

Abstract read
In one paragraph

Article in Biometrical journal. Biometrische Zeitschrift, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  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

5 authors.

Pavla KrotkaCenter for Medical Data Science, Medical University of Vienna, Vienna, Austria.ORCID 0000-0001-5727-4270
Martin PoschCenter for Medical Data Science, Medical University of Vienna, Vienna, Austria.
Mohamed GewilyDepartment of Pharmacy, Uppsala University, Uppsala, Sweden.
Günter HöglingerDepartment of Neurology, LMU University Hospital, Ludwig-Maximilians-Universität (LMU) München, Munich, Germany.
Marta Bofill RoigCenter for Medical Data Science, Medical University of Vienna, Vienna, Austria.ORCID 0000-0002-4400-7541

Funding

Austrian Science Fund ESP 442 ESPRIT-ProgrammDeutsche Forschungsgemeinschaft EXC 2145 SyNergy - ID 390857198European Joint Programme on Rare Diseases Improve-PSPSwedish Research Council 2018-03317
6 · The paper itself

Abstract

Utilizing non-concurrent control (NCC) data in the analysis of late-entering arms in platform trials has recently received considerable attention. While incorporating NCC can lead to increased power and lower sample sizes, it might introduce bias to the effect estimators if temporal drifts are present. Aiming to mitigate this potential bias, we propose various frequentist model-based approaches that leverage the NCC, while adjusting for time. One of the currently available models incorporates time as a categorical fixed effect, separating the trial duration into periods, defined as time intervals bounded by any arm entering or leaving the platform. In this work, we propose two extensions of this model. First, we consider an alternative definition of time by dividing the trial into fixed-length calendar time intervals. Second, we propose alternative model-based time adjustments. Specifically, we investigate adjusting for random effects and employing splines to model time with a polynomial function. We evaluate the performance of the proposed approaches in a simulation study and illustrate their use through a case study. We show that adjusting for time via a spline function controls the type I error in trials with a sufficiently smooth time trend pattern and may lead to power gains compared to the standard fixed effect model. However, the fixed effect model with period adjustment is the most robust model for arbitrary time trends, provided that the trend is equal across all arms. Especially, in trials with sudden changes in the time trend, the period-adjustment model is preferred if NCCs are included.

Indexed as

BiometryClinical Trials as TopicModels, StatisticalHumansTime Factorsnon‐concurrent controlsplatform trialsstatistical modelingtime trends

Identifiers

PMID40491339
PMCPMC12150008

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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.