Evidence map›Paper›PMID 42252652›Full record

ArticleStatistics in medicine2026

Empirical Comparison of Win Ratio and Joint Frailty Models for Recurrent Event Endpoints With Applications in Oncology and Cardiology.

Adrien Orué, Derek Dinart, Laurent Billot, Carine Bellera, Virginie Rondeau

Abstract readComparative Study
In one paragraph

Article in Statistics in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Adrien OruéDepartment of Biostatistics, Bordeaux Population Health Research Center, INSERM U1219, Université de Bordeaux, Bordeaux, France.ORCID https://orcid.org/0009-0003-4041-5016
Derek DinartClinical and Epidemiological Research Unit, Institut Bergonié, Comprehensive Cancer Center, Inserm CIC1401, Bordeaux, France.
Laurent BillotThe George Institute for Global Health, Faculty of Medicine and Health, University of New South Wales, Sydney, Australia.
Carine BelleraClinical and Epidemiological Research Unit, Institut Bergonié, Comprehensive Cancer Center, Inserm CIC1401, Bordeaux, France.
Virginie RondeauDepartment of Biostatistics, Bordeaux Population Health Research Center, INSERM U1219, Université de Bordeaux, Bordeaux, France.

Funding

Institut National Du Cancer 18610
6 · The paper itself

Abstract

Composite endpoints that combine recurrent non-fatal events with a terminal event are increasingly used in randomized clinical trials, yet conventional time-to-first event analyses may obscure clinically relevant information. We compared two statistical frameworks tailored to such endpoints: the joint frailty model (JFM) and the last-event assisted recurrent-event win ratio (LWR). The JFM specifies proportional hazards for the recurrent and terminal events linked through a shared frailty, yielding covariate-adjusted, component-specific hazard ratios that account for informative recurrences and dependence with death. The LWR is a nonparametric, prioritized pairwise comparison that incorporates all observed events over follow-up and summarizes a population-level benefit of treatment while respecting a pre-specified hierarchy between death and recurrences. We first assessed the performance of the methods using simulations that varied both the gamma-frailty variance and the event rates. We next illustrated both approaches using two clinical application examples in oncology and cardiology, highlighting how conclusions depend on whether treatment primarily affects recurrent events, mortality, or both. The JFM provided component-specific estimates, while the LWR led to a summary measure of treatment effect with direction. Power was systematically improved with JFM, which thus appeared as the most reliable approach for inference and sample size estimation. Methodological extensions of the LWR to appropriately handle censoring and to formalize causal estimands remain a promising direction for future research.

Indexed as

CardiologyEndpoint DeterminationMedical OncologyModels, StatisticalRandomized Controlled Trials as TopicComputer SimulationFrailtyHumansProportional Hazards ModelsRecurrencecardiologyjoint frailty modelsoncologypowerrandomized clinical trialsrecurrent eventssample sizewin ratio

Identifiers

PMID42252652
PMCPMC13243822

What OpenQuestion holds

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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.