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dc.contributor.authorEastwood, M
dc.contributor.authorMarc, ST
dc.contributor.authorGao, X
dc.contributor.authorSailem, H
dc.contributor.authorOffman, J
dc.contributor.authorKarteris, E
dc.contributor.authorFernandez, AM
dc.contributor.authorJonigk, D
dc.contributor.authorCookson, W
dc.contributor.authorMoffatt, M
dc.contributor.authorPopat, S
dc.contributor.authorMinhas, F
dc.contributor.authorRobertus, JL
dc.coverage.spatialNetherlands
dc.date.accessioned2023-10-02T11:36:26Z
dc.date.available2023-10-02T11:36:26Z
dc.date.issued2023-09-01
dc.identifierARTN 102628
dc.identifierS0933-3657(23)00142-2
dc.identifier.citationArtificial Intelligence in Medicine, 2023, 143 pp. 102628 -en_US
dc.identifier.issn0933-3657
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/6004
dc.identifier.eissn1873-2860
dc.identifier.eissn1873-2860
dc.identifier.doi10.1016/j.artmed.2023.102628
dc.description.abstractMalignant Mesothelioma is a difficult to diagnose and highly lethal cancer usually associated with asbestos exposure. It can be broadly classified into three subtypes: Epithelioid, Sarcomatoid, and a hybrid Biphasic subtype in which significant components of both of the previous subtypes are present. Early diagnosis and identification of the subtype informs treatment and can help improve patient outcome. However, the subtyping of malignant mesothelioma, and specifically the recognition of transitional features from routine histology slides has a high level of inter-observer variability. In this work, we propose an end-to-end multiple instance learning (MIL) approach for malignant mesothelioma subtyping. This uses an adaptive instance-based sampling scheme for training deep convolutional neural networks on bags of image patches that allows learning on a wider range of relevant instances compared to max or top-N based MIL approaches. We also investigate augmenting the instance representation to include aggregate cellular morphology features from cell segmentation. The proposed MIL approach enables identification of malignant mesothelial subtypes of specific tissue regions. From this a continuous characterisation of a sample according to predominance of sarcomatoid vs epithelioid regions is possible, thus avoiding the arbitrary and highly subjective categorisation by currently used subtypes. Instance scoring also enables studying tumor heterogeneity and identifying patterns associated with different subtypes. We have evaluated the proposed method on a dataset of 234 tissue micro-array cores with an AUROC of 0.89±0.05 for this task. The dataset and developed methodology is available for the community at: https://github.com/measty/PINS.
dc.formatPrint-Electronic
dc.format.extent102628 -
dc.languageeng
dc.language.isoengen_US
dc.publisherELSEVIERen_US
dc.relation.ispartofArtificial Intelligence in Medicine
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectCancer subtyping
dc.subjectComputational pathology
dc.subjectDeep learning
dc.subjectMalignant Mesothelioma
dc.subjectMultiple instance learning
dc.subjectHumans
dc.subjectMesothelioma, Malignant
dc.subjectNeural Networks, Computer
dc.subjectRecognition, Psychology
dc.titleMalignant Mesothelioma subtyping via sampling driven multiple instance prediction on tissue image and cell morphology data.en_US
dc.typeJournal Article
dcterms.dateAccepted2023-07-14
dc.date.updated2023-10-02T11:35:59Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1016/j.artmed.2023.102628en_US
rioxxterms.licenseref.startdate2023-09-01
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/37673586
pubs.organisational-groupICR
pubs.organisational-groupICR/Primary Group
pubs.organisational-groupICR/Primary Group/ICR Divisions
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology
pubs.organisational-groupICR/Primary Group/ICR Divisions/Clinical Studies/Thoracic Oncology/Thoracic Oncology (hon.)
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1016/j.artmed.2023.102628
pubs.volume143
dc.contributor.icrauthorPopat, Sanjay
icr.provenanceDeposited by Mr Arek Surman on 2023-10-02. Deposit type is initial. No. of files: 1. Files: 1-s2.0-S0933365723001422-main.pdf


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