Evidence map›Paper›PMID 40705274›Full record

ArticlePhysical and engineering sciences in medicine2025

An approach for cancer outcomes modelling using a comprehensive synthetic dataset.

Lorna Tu, Hervé H F Choi, Haley Clark, Samantha A M Lloyd

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Article in Physical and engineering sciences in medicine, 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

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Lorna TuDepartment of Physics and Astronomy, University of British Columbia, Vancouver, BC, Canada. lornatu@phas.ubc.ca.ORCID https://orcid.org/0000-0002-6902-8998
Hervé H F ChoiDepartment of Medical Physics, BC Cancer - Vancouver, Vancouver, BC, Canada.
Haley ClarkDepartment of Physics and Astronomy, University of British Columbia, Vancouver, BC, Canada.
Samantha A M LloydDepartment of Physics and Astronomy, University of British Columbia, Vancouver, BC, Canada.

Funding

Natural Sciences and Engineering Research Council of Canada PGS D- 579626- 2023
6 · The paper itself

Abstract

Limited patient data availability presents a challenge for efficient machine learning (ML) model development. Recent studies have proposed methods to generate synthetic medical images but lack the corresponding prognostic information required for predicting outcomes. We present a cancer outcomes modelling approach that involves generating a comprehensive synthetic dataset which can accurately mimic a real dataset. A real public dataset containing computed tomography-based radiomic features and clinical information for 132 non-small cell lung cancer patients was used. A synthetic dataset of virtual patients was synthesized using a conditional tabular generative adversarial network. Models to predict two-year overall survival were trained on real or synthetic data using combinations of four feature selection methods (mutual information, ANOVA F-test, recursive feature elimination, random forest (RF) importance weights) and six ML algorithms (RF, k-nearest neighbours, logistic regression, support vector machine, XGBoost, Gaussian Naïve Bayes). Models were tested on withheld real data and externally validated. Real and synthetic datasets were similar, with an average one minus Kolmogorov-Smirnov test statistic of 0.871 for continuous features. Chi-square test confirmed agreement for discrete features (p < 0.001). XGBoost using RF importance-based features performed the most consistently for both datasets, with percent differences in balanced accuracy and area under the precision-recall curve of < 1.3%. Preliminary findings demonstrate the potential application of synthetic radiomic and clinical data augmentation for cancer outcomes modelling, although further validation with larger diverse datasets is crucial. While our approach was described in a lung context, it may be applied to other sites or endpoints.

Indexed as

Lung NeoplasmsAgedAlgorithmsCarcinoma, Non-Small-Cell LungFemaleHumansMachine LearningMaleMiddle AgedPrognosisSupport Vector MachineTomography, X-Ray ComputedTreatment OutcomeData augmentationNon-small cell lung cancerOutcomes predictionOverall survivalRadiomicsSynthetic data

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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.