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dc.contributor.authorNallala, J
dc.contributor.authorGriggs, R
dc.contributor.authorLloyd, GR
dc.contributor.authorStone, N
dc.contributor.authorShepherd, NA
dc.date.accessioned2022-05-10T09:03:56Z
dc.date.issued2022-04-28
dc.date.updated2022-05-09T15:23:30Z
dc.description.abstractPurpose: The differential diagnosis of epithelial misplacement from invasive cancer in the colon is a challenging endeavour, augmented by the introduction of bowel cancer population screening. The main aim of the work is to test, as a proof-of concept study, the ability of the infrared spectroscopic imaging approach to differentiate epithelial misplacement from adenocarcinoma in sigmoid colonic adenomatous polyps. Methods: Ten samples from each of the four diagnostic groups, normal colonic mucosa, adenomatous polyps with low grade dysplasia, epithelial misplacement in adenomatous polyps and adenocarcinoma, were analysed using IR spectroscopic imaging and data processing methods. IR spectral images were subjected to data pre-processing and cluster analysis based segmentation to identify epithelial, connective tissue and stromal regions. Statistical analysis was carried out using principal component analysis and linear discriminant analysis based cross validation, to classify spectral features according to the pathology, and the diagnostic attributes were compared. Results: The combined 4-group classification model on an average showed a sensitivity of 64%, a specificity of 88% and an accuracy of 76% for prediction based on a ‘single spectrum’, whilst a ‘majority-vote’ prediction on an average showed a sensitivity of 73%, a specificity of 90% and an accuracy of 82%. The 2-group model, for the differential diagnosis of epithelial misplacement versus adenocarcinoma, showed an average sensitivity and specificity of 82.5% for prediction based on a ‘single spectrum’ whilst a ‘majority-vote’ classification showed an average sensitivity and specificity of 90%. A 92% area under the curve (AUC) value was obtained when evaluating the classifier using the Receiver Operating Characteristics (ROC) curves. Conclusions: IR spectroscopy shows promise in its ability to differentiate epithelial misplacement from adenocarcinoma in tissue sections, considered as one of the most challenging endeavours in population-wide diagnostic histopathology. Further studies with larger series, including cases with challenging diagnostic features are required to ascertain the capability of this modern digital pathology approach. In the long-term, IR spectroscopy based pathology which is relatively low-cost and rapid, could be a promising endeavour to consider for integration into the existing histopathology pathway, in particular for population based screening programmes where large number of samples are scrutinised.en_GB
dc.description.sponsorshipNational Institute for Health Research (NIHR)en_GB
dc.format.extent2632010x221088960-
dc.identifier.citationVol. 15en_GB
dc.identifier.doihttps://doi.org/10.1177/2632010x221088960
dc.identifier.grantnumberCSA/03/07/017en_GB
dc.identifier.urihttp://hdl.handle.net/10871/129573
dc.identifierORCID: 0000-0002-9473-5782 (Nallala, Jayakrupakar)
dc.language.isoenen_GB
dc.publisherSAGE Publicationsen_GB
dc.rights© The Author(s) 2022. Open access. This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).en_GB
dc.subjectEpithelial misplacementen_GB
dc.subjectpseudo-invasionen_GB
dc.subjectadenocarcinomaen_GB
dc.subjectsigmoid colonen_GB
dc.subjectinfra-red spectroscopyen_GB
dc.subjectspectral histopathologyen_GB
dc.titleInfrared Spectroscopic Analysis in the Differentiation of Epithelial Misplacement From Adenocarcinoma in Sigmoid Colonic Adenomatous Polypsen_GB
dc.typeArticleen_GB
dc.date.available2022-05-10T09:03:56Z
dc.identifier.issn2632-010X
dc.descriptionThis is the final version. Available on open access from SAGE Publications via the DOI in this recorden_GB
dc.descriptionAvailability of Data and Material: The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable requesten_GB
dc.identifier.eissn2632-010X
dc.identifier.journalClinical Pathologyen_GB
dc.relation.ispartofClinical Pathology, 15
dc.rights.urihttps://creativecommons.org/licenses/by/4.0en_GB
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2022-04-25
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-05-10T08:28:35Z
refterms.versionFCDVoR
refterms.dateFOA2025-03-06T23:14:54Z
refterms.panelBen_GB
refterms.dateFirstOnline2022-04-28


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© The Author(s) 2022. Open access. This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
Except where otherwise noted, this item's licence is described as © The Author(s) 2022. Open access. This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).