Evidence map›Paper›PMID 40165441›Full record

ArticleStatistical methods in medical research2025

A Weibull mixture cure frailty model for high-dimensional covariates.

Fatih Kızılaslan, David Michael Swanson, Valeria Vitelli

Abstract read
In one paragraph

Article in Statistical methods in medical research, 2025. 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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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Fatih KızılaslanOslo Centre for Biostatistics and Epidemiology, Department of Biostatistics, University of Oslo, Norway.
David Michael SwansonDepartment of Biostatistics, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.ORCID 0000-0003-3174-1656
Valeria VitelliOslo Centre for Biostatistics and Epidemiology, Department of Biostatistics, University of Oslo, Norway.ORCID 0000-0002-6746-0453

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A novel mixture cure frailty model is introduced for handling censored survival data. Mixture cure models are preferable when the existence of a cured fraction among patients can be assumed. However, such models are heavily underexplored: frailty structures within cure models remain largely undeveloped, and furthermore, most existing methods do not work for high-dimensional datasets, when the number of predictors is significantly larger than the number of observations. In this study, we introduce a novel extension of the Weibull mixture cure model that incorporates a frailty component, employed to model an underlying latent population heterogeneity with respect to the outcome risk. Additionally, high-dimensional covariates are integrated into both the cure rate and survival part of the model, providing a comprehensive approach to employ the model in the context of high-dimensional omics data. We also perform variable selection via an adaptive elastic-net penalization, and propose a novel approach to inference using the expectation-maximization (EM) algorithm. Extensive simulation studies are conducted across various scenarios to demonstrate the performance of the model, and results indicate that our proposed method outperforms competitor models. We apply the novel approach to analyze RNAseq gene expression data from bulk breast cancer patients included in The Cancer Genome Atlas (TCGA) database. A set of prognostic biomarkers is then derived from selected genes, and subsequently validated via both functional enrichment analysis and comparison to the existing biological literature. Finally, a prognostic risk score index based on the identified biomarkers is proposed and validated by exploring the patients' survival.

Indexed as

Models, StatisticalAlgorithmsBreast NeoplasmsComputer SimulationFemaleFrailtyHumansSurvival Analysisadaptive elastic-netbiomarker discoveryexpectation–maximization methodMixture cure frailty modelvariable selection

Identifiers

PMID40165441
PMCPMC12209551

What Socratic holds

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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 Socratic graph.