Evidence map›Paper›PMID 42611869›Full record

ArticlePloS one2026

Evaluating the impact of segmentation strategies on radiomic feature stability for paediatric brain tumour diagnosis using diffusion weighted imaging.

Timothy Mulvany, Daniel Griffiths-King, Lara Worthington, Katherine Crombie, Heather E L Rose, Andrew Peet, John Apps, Jan Novak

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Article in PloS one, 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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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

8 authors.

Timothy MulvanyAston Institute of Health and Neurodevelopment, Aston University, Birmingham, United Kingdom.ORCID https://orcid.org/0009-0000-1699-4415
Daniel Griffiths-KingAston Institute of Health and Neurodevelopment, Aston University, Birmingham, United Kingdom.
Lara WorthingtonDepartment of Oncology, Birmingham Women's and Children's Hospital NHS Foundation Trust, Birmingham, United Kingdom.
Katherine CrombieInstitute of Cancer & Genomics Science, University of Birmingham, Birmingham, United Kingdom.ORCID https://orcid.org/0009-0006-4405-7561
Heather E L RoseMedical Physics Nottingham University Hospitals NHS Trust, Nottingham, United Kingdom.ORCID https://orcid.org/0000-0002-0346-1334
Andrew PeetDepartment of Oncology, Birmingham Women's and Children's Hospital NHS Foundation Trust, Birmingham, United Kingdom.
John AppsDepartment of Oncology, Birmingham Women's and Children's Hospital NHS Foundation Trust, Birmingham, United Kingdom.
Jan NovakAston Institute of Health and Neurodevelopment, Aston University, Birmingham, United Kingdom.ORCID https://orcid.org/0000-0001-5173-3608

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThis research aims to comprehensively assess the impact of both conservatively and extensively delineated Regions of Interest (ROI) on subsequent quantitative in-vivo characterisation of paediatric brain tumours using diffusion-weighted MRI.

methodsUtilising a retrospective cohort of 106 paediatric brain tumour patients, ground truth (GT) ROIs delineating tumour boundaries were eroded or dilated, simulating conservative and extensive ROI drawing strategies respectively. Stability was evaluated for 19 first-order radiomic features extracted from Apparent Diffusion Coefficient (ADC) maps within each ROI. Further, these features were used to train a series of machine learning models to evaluate the impact of ROI boundaries on downstream diagnostic classification.

resultsFor 18/19 first-order features, ROI dilation introduced significantly (p < 0.01) greater feature variability than erosion, with large effect size (d > 0.8) for 11 features. This relationship was variable between diagnoses, and strongest amongst pilocytic astrocytomas. Diagnostic models trained using features from GT ROIs were negatively impacted with classification accuracy reduced by 3.8 ± 0.8% and 5.6 ± 0.9% for low-level erosion and dilation respectively. Inclusion of eroded/dilated ROI features into the training dataset combined with stable-feature selection partially mitigated the impact of erosion/dilation on model accuracy with 1.4 ± 0.7% and 2.9 ± 0.3% accuracy drop compared model accuracy on features extracted from GT ROIs.

conclusionThe consistently reduced impact of conservative boundaries over extensive ones suggests that, in terms of segmentation strategies, exclusion of ambiguous boundary regions may be preferable over their inclusion. Additionally, diagnostic models exhibited improved robustness to variable ROI drawing strategies through training augmentation and selection of stable features.

Indexed as

Brain NeoplasmsDiffusion Magnetic Resonance ImagingAdolescentChildChild, PreschoolFemaleHumansImage Processing, Computer-AssistedMachine LearningMaleRadiomicsRetrospective Studies

Identifiers

PMID42611869
PMCPMC13484970

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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.