Evidence map›Paper›PMID 42373934›Full record

ArticleTherapeutic innovation & regulatory science2026

The Effect of Covariate Adjustment for Cox Regression in Cardiovascular Outcome Trials.

Alexander Przybylski, Björn Holzhauer, Simon Wandel

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Article in Therapeutic innovation & regulatory science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Alexander PrzybylskiNovartis Pharmaceuticals UK Ltd., London, UK. alexander.przybylski@novartis.com.
Björn HolzhauerNovartis Pharma AG, Basel, Switzerland.
Simon WandelNovartis Pharma AG, Basel, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adjustment for prognostic baseline covariates is routinely used to increase power in randomized controlled trials. Yet, time-to-event outcomes are commonly analyzed using the log-rank test or Cox regression with no covariates besides treatment. Covariate adjustment in non-linear models is more complex than in linear models: effect measures such as hazard ratios are non-collapsible, risk scores may be weakly prognostic, and misspecification can inflate type I error. Nine cardiovascular outcome trials were re-analyzed with adjustment for existing risk scores and known prognostic factors. We also assessed whether adjustment for these covariates would be outperformed by adjustment for predictions from newly created models (so-called 'super covariates'). In addition to conditional Cox model analyses, marginal treatment effects were compared. We evaluated the strength of prognostic covariates required for adjustment to be worthwhile using simulations. Adjustment for existing risk scores and known prognostic factors had minimal impact on treatment effect estimates. Adjusting for newly developed model-based predictions on average improved conditional test statistics, but not consistently across studies or cross-validation folds. While the model-based predictions were stronger prognostic factors, variability of the gain in test statistic also increased. Efficiency gains for marginal estimates were consistent but modest. The simulations suggest that stronger prognostic covariates than the existing or our newly developed risk scores are required for greater efficiency gains. For cardiovascular outcome trials, covariate adjustment should be used more often, but one should assess the potential benefits carefully to avoid unrealistic expectations or unwarranted reductions in the target number of patients with an event.

Indexed as

Cardiovascular DiseasesRandomized Controlled Trials as TopicHumansPrognosisProportional Hazards ModelsCardiovascular outcome trialsCovariate adjustmentCox regressionSuper-covariatesTime-to-event

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Registered trials

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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.