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Mid-Infrared Imaging Characterization to Differentiate Lung Cancer Subtypes

Introduction: Lung cancer is the most common malignancy worldwide. Squamous cell carcinoma (SQ) and adenocarcinoma (LUAD) are the two most frequent histological subtypes. Small cell carcinoma (SCLC) subtype has the worst prognosis. Differential diagnosis is essential for proper oncological treatment...

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Autores principales: Kontsek, E., Pesti, A., Slezsák, J., Gordon, P., Tornóczki, T., Smuk, G., Gergely, S., Kiss, A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428038/
https://www.ncbi.nlm.nih.gov/pubmed/36061143
http://dx.doi.org/10.3389/pore.2022.1610439
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author Kontsek, E.
Pesti, A.
Slezsák, J.
Gordon, P.
Tornóczki, T.
Smuk, G.
Gergely, S.
Kiss, A.
author_facet Kontsek, E.
Pesti, A.
Slezsák, J.
Gordon, P.
Tornóczki, T.
Smuk, G.
Gergely, S.
Kiss, A.
author_sort Kontsek, E.
collection PubMed
description Introduction: Lung cancer is the most common malignancy worldwide. Squamous cell carcinoma (SQ) and adenocarcinoma (LUAD) are the two most frequent histological subtypes. Small cell carcinoma (SCLC) subtype has the worst prognosis. Differential diagnosis is essential for proper oncological treatment. Life science associated mid- and near-infrared based microscopic techniques have been developed exponentially, especially in the past decade. Vibrational spectroscopy is a potential non-destructive approach to investigate malignancies. Aims: Our goal was to differentiate lung cancer subtypes by their label-free mid-infrared spectra using supervised multivariate analyses. Material and Methods: Formalin-fixed paraffin-embedded (FFPE) samples were selected from the archives. Three subtypes were selected for each group: 10-10 cases SQ, LUAD and SCLC. 2 μm thick sections were cut and laid on aluminium coated glass slides. Transflection optical setup was applied on Perkin-Elmer infrared microscope. 250 × 600 μm areas were imaged and the so-called mid-infrared fingerprint region (1800-648cm(−1)) was further analysed with linear discriminant analysis (LDA) and support vector machine (SVM) methods. Results: Both “patient-based” and “pixel-based” approaches were examined. Patient-based analysis by using 3 LDA models and 2 SVM models resulted in different separations. The higher the cut-off value the lower is the accuracy. The linear C-support vector classification (C-SVC) SVM resulted in the best (100%) accuracy for the three subtypes using a 50% cut-off value. The pixel-based analysis gave, similarly, the linear C-SVC SVM model to be the most efficient in the statistical indicators (SQ sensitivity 81.65%, LUAD sensitivity 82.89% and SCLC sensitivity 88.89%). The spectra cut-off, the kernel function and the algorithm function influence the accuracy. Conclusion: Mid-Infrared imaging could be used to differentiate FFPE lung cancer subtypes. Supervised multivariate tools are promising to accurately separate lung tumor subtypes. The long-term perspective is to develop a spectroscopy-based diagnostic tool, revolutionizing medical differential diagnostics, especially cancer identification.
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spelling pubmed-94280382022-09-01 Mid-Infrared Imaging Characterization to Differentiate Lung Cancer Subtypes Kontsek, E. Pesti, A. Slezsák, J. Gordon, P. Tornóczki, T. Smuk, G. Gergely, S. Kiss, A. Pathol Oncol Res Pathology and Oncology Archive Introduction: Lung cancer is the most common malignancy worldwide. Squamous cell carcinoma (SQ) and adenocarcinoma (LUAD) are the two most frequent histological subtypes. Small cell carcinoma (SCLC) subtype has the worst prognosis. Differential diagnosis is essential for proper oncological treatment. Life science associated mid- and near-infrared based microscopic techniques have been developed exponentially, especially in the past decade. Vibrational spectroscopy is a potential non-destructive approach to investigate malignancies. Aims: Our goal was to differentiate lung cancer subtypes by their label-free mid-infrared spectra using supervised multivariate analyses. Material and Methods: Formalin-fixed paraffin-embedded (FFPE) samples were selected from the archives. Three subtypes were selected for each group: 10-10 cases SQ, LUAD and SCLC. 2 μm thick sections were cut and laid on aluminium coated glass slides. Transflection optical setup was applied on Perkin-Elmer infrared microscope. 250 × 600 μm areas were imaged and the so-called mid-infrared fingerprint region (1800-648cm(−1)) was further analysed with linear discriminant analysis (LDA) and support vector machine (SVM) methods. Results: Both “patient-based” and “pixel-based” approaches were examined. Patient-based analysis by using 3 LDA models and 2 SVM models resulted in different separations. The higher the cut-off value the lower is the accuracy. The linear C-support vector classification (C-SVC) SVM resulted in the best (100%) accuracy for the three subtypes using a 50% cut-off value. The pixel-based analysis gave, similarly, the linear C-SVC SVM model to be the most efficient in the statistical indicators (SQ sensitivity 81.65%, LUAD sensitivity 82.89% and SCLC sensitivity 88.89%). The spectra cut-off, the kernel function and the algorithm function influence the accuracy. Conclusion: Mid-Infrared imaging could be used to differentiate FFPE lung cancer subtypes. Supervised multivariate tools are promising to accurately separate lung tumor subtypes. The long-term perspective is to develop a spectroscopy-based diagnostic tool, revolutionizing medical differential diagnostics, especially cancer identification. Frontiers Media S.A. 2022-08-17 /pmc/articles/PMC9428038/ /pubmed/36061143 http://dx.doi.org/10.3389/pore.2022.1610439 Text en Copyright © 2022 Kontsek, Pesti, Slezsák, Gordon, Tornóczki, Smuk, Gergely and Kiss. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pathology and Oncology Archive
Kontsek, E.
Pesti, A.
Slezsák, J.
Gordon, P.
Tornóczki, T.
Smuk, G.
Gergely, S.
Kiss, A.
Mid-Infrared Imaging Characterization to Differentiate Lung Cancer Subtypes
title Mid-Infrared Imaging Characterization to Differentiate Lung Cancer Subtypes
title_full Mid-Infrared Imaging Characterization to Differentiate Lung Cancer Subtypes
title_fullStr Mid-Infrared Imaging Characterization to Differentiate Lung Cancer Subtypes
title_full_unstemmed Mid-Infrared Imaging Characterization to Differentiate Lung Cancer Subtypes
title_short Mid-Infrared Imaging Characterization to Differentiate Lung Cancer Subtypes
title_sort mid-infrared imaging characterization to differentiate lung cancer subtypes
topic Pathology and Oncology Archive
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9428038/
https://www.ncbi.nlm.nih.gov/pubmed/36061143
http://dx.doi.org/10.3389/pore.2022.1610439
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