Evidence map›Paper›PMID 42120646›Full record

ArticleLifetime data analysis2026

Gradient boosting-based discrete failure time model for selecting time-varying effects and interactions.

Lingfeng Luo, Kevin He, Jeremy M G Taylor

Abstract read
In one paragraph

Article in Lifetime data analysis, 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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0citing papers in PubMed
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1 · What the graph read from it

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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.

Lingfeng LuoDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA.
Kevin HeDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA.
Jeremy M G TaylorDepartment of Biostatistics, University of Michigan, Ann Arbor, MI, USA. jmgt@umich.edu.ORCID http://orcid.org/0000-0003-2791-1229

Funding

Statistical Methods for Cancer BiomarkersR01CA129102 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI GHOSH, DEBASHIS, TAYLOR, JEREMY M.G. · 2009 to 2021
$3.3M
Improve Statistical Methods for Profiling of Healthcare ProvidersR01DK129539 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Zhi Kevin He · 2022 to 2026
$1.6M
NCI NIH HHS R01 CA129102NIDDK NIH HHS R01 DK129539NIH HHS CA-129102NIH HHS DK-129539.
6 · The paper itself

Abstract

Analyzing survival data from the National Cancer Institute's Surveillance, Epidemiology, and End Results (SEER) Program offers invaluable insight to guide cancer management. In these data the event times are recorded in units of months. In such datasets, it can be important to consider the selection of covariates, distinguish between time-varying and time-independent effects, and capture important interaction terms. However, variable selection is difficult to combine with the differentiation between time-varying and time-independent effects. Moreover, accurately selecting interaction terms is more challenging because of the hierarchy restriction that an interaction term should only enter a model if one or both associated main effects are also included. To resolve these issues, we develop a coordinate ascent-based gradient boosting procedure for discrete failure time models. This approach achieves variable selection in high-dimensional settings, differentiates between time-varying and time-independent variables, and selects important interaction terms under hierarchy restrictions. Traditional boosting stopping criteria are ad hoc, while preferable information-criteria-based rules necessitate defining degrees of freedom, a challenge in survival models. Our approach provides well-defined degrees of freedom and offers information-criteria-based stopping rules. Simulation studies show the proposed method achieves good selection performance. We apply the proposed method to SEER melanoma cancer data and select important risk factors, distinguish between time-varying and time-dependent effects and detect important two-way interactions.

Indexed as

Models, StatisticalBoosting Machine Learning AlgorithmsComputer SimulationHumansSEER ProgramSurvival AnalysisTime FactorsDiscrete failure timeHierarchical interactionsHigh dimensional variable selectionSurvival analysisTime-varying effects

Identifiers

PMID42120646
PMCPMC13167897

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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.