Evidence map›Paper›PMID 28754093›Full record

ArticleBMC medical research methodology2017

A comparison of the conditional inference survival forest model to random survival forests based on a simulation study as well as on two applications with time-to-event data.

Justine B Nasejje, Henry Mwambi, Keertan Dheda, Maia Lesosky

Abstract readComparative Study
In one paragraph

Article in BMC medical research methodology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

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39citing papers 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

The trial behind it

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3 · Its place in the literature

Who cites it

39 citing papers in PubMed.

  1. Scientific reports · 2020
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  4. Survival-LCS: Rule-Based Survival Analysis without Proportional Hazard Assumptions.ACM transactions on evolutionary learning and optimization · 2026
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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Justine B NasejjeSchool of Statistics, Mathematics and Computer Science, University of Kwazulu-Natal, Pietermaritzburg, South Africa. justinenasejje@gmail.com.
Henry MwambiSchool of Statistics, Mathematics and Computer Science, University of Kwazulu-Natal, Pietermaritzburg, South Africa.
Keertan DhedaDivision of Pulmonology and UCT Lung Institute, Department of Medicine, University of Cape Town, Cape Town, South Africa.
Maia LesoskyDivision of Epidemiology and Biostatistics, School of Public Health and Family Medicine, University of Cape Town, Cape Town, South Africa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRandom survival forest (RSF) models have been identified as alternative methods to the Cox proportional hazards model in analysing time-to-event data. These methods, however, have been criticised for the bias that results from favouring covariates with many split-points and hence conditional inference forests for time-to-event data have been suggested. Conditional inference forests (CIF) are known to correct the bias in RSF models by separating the procedure for the best covariate to split on from that of the best split point search for the selected covariate.

methodsIn this study, we compare the random survival forest model to the conditional inference model (CIF) using twenty-two simulated time-to-event datasets. We also analysed two real time-to-event datasets. The first dataset is based on the survival of children under-five years of age in Uganda and it consists of categorical covariates with most of them having more than two levels (many split-points). The second dataset is based on the survival of patients with extremely drug resistant tuberculosis (XDR TB) which consists of mainly categorical covariates with two levels (few split-points).

resultsThe study findings indicate that the conditional inference forest model is superior to random survival forest models in analysing time-to-event data that consists of covariates with many split-points based on the values of the bootstrap cross-validated estimates for integrated Brier scores. However, conditional inference forests perform comparably similar to random survival forests models in analysing time-to-event data consisting of covariates with fewer split-points.

conclusionAlthough survival forests are promising methods in analysing time-to-event data, it is important to identify the best forest model for analysis based on the nature of covariates of the dataset in question.

Indexed as

AlgorithmsModels, StatisticalProportional Hazards ModelsSurvival AnalysisChildDrug ResistanceHumansTuberculosisUgandaConditional inference forestsRandom survival forestsSplit-pointsSurvival analysisSurvival trees

Identifiers

PMID28754093
PMCPMC5534080

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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.