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Automated tumor analysis for molecular profiling in lung cancer

The discovery and clinical application of molecular biomarkers in solid tumors, increasingly relies on nucleic acid extraction from FFPE tissue sections and subsequent molecular profiling. This in turn requires the pathological review of haematoxylin & eosin (H&E) stained slides, to ensure s...

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Autores principales: Hamilton, Peter W., Wang, Yinhai, Boyd, Clinton, James, Jacqueline A., Loughrey, Maurice B., Hougton, Joseph P., Boyle, David P., Kelly, Paul, Maxwell, Perry, McCleary, David, Diamond, James, McArt, Darragh G., Tunstall, Jonathon, Bankhead, Peter, Salto-Tellez, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4695036/
https://www.ncbi.nlm.nih.gov/pubmed/26317646
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author Hamilton, Peter W.
Wang, Yinhai
Boyd, Clinton
James, Jacqueline A.
Loughrey, Maurice B.
Hougton, Joseph P.
Boyle, David P.
Kelly, Paul
Maxwell, Perry
McCleary, David
Diamond, James
McArt, Darragh G.
Tunstall, Jonathon
Bankhead, Peter
Salto-Tellez, Manuel
author_facet Hamilton, Peter W.
Wang, Yinhai
Boyd, Clinton
James, Jacqueline A.
Loughrey, Maurice B.
Hougton, Joseph P.
Boyle, David P.
Kelly, Paul
Maxwell, Perry
McCleary, David
Diamond, James
McArt, Darragh G.
Tunstall, Jonathon
Bankhead, Peter
Salto-Tellez, Manuel
author_sort Hamilton, Peter W.
collection PubMed
description The discovery and clinical application of molecular biomarkers in solid tumors, increasingly relies on nucleic acid extraction from FFPE tissue sections and subsequent molecular profiling. This in turn requires the pathological review of haematoxylin & eosin (H&E) stained slides, to ensure sample quality, tumor DNA sufficiency by visually estimating the percentage tumor nuclei and tumor annotation for manual macrodissection. In this study on NSCLC, we demonstrate considerable variation in tumor nuclei percentage between pathologists, potentially undermining the precision of NSCLC molecular evaluation and emphasising the need for quantitative tumor evaluation. We subsequently describe the development and validation of a system called TissueMark for automated tumor annotation and percentage tumor nuclei measurement in NSCLC using computerized image analysis. Evaluation of 245 NSCLC slides showed precise automated tumor annotation of cases using Tissuemark, strong concordance with manually drawn boundaries and identical EGFR mutational status, following manual macrodissection from the image analysis generated tumor boundaries. Automated analysis of cell counts for % tumor measurements by Tissuemark showed reduced variability and significant correlation (p < 0.001) with benchmark tumor cell counts. This study demonstrates a robust image analysis technology that can facilitate the automated quantitative analysis of tissue samples for molecular profiling in discovery and diagnostics.
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spelling pubmed-46950362016-01-20 Automated tumor analysis for molecular profiling in lung cancer Hamilton, Peter W. Wang, Yinhai Boyd, Clinton James, Jacqueline A. Loughrey, Maurice B. Hougton, Joseph P. Boyle, David P. Kelly, Paul Maxwell, Perry McCleary, David Diamond, James McArt, Darragh G. Tunstall, Jonathon Bankhead, Peter Salto-Tellez, Manuel Oncotarget Research Paper The discovery and clinical application of molecular biomarkers in solid tumors, increasingly relies on nucleic acid extraction from FFPE tissue sections and subsequent molecular profiling. This in turn requires the pathological review of haematoxylin & eosin (H&E) stained slides, to ensure sample quality, tumor DNA sufficiency by visually estimating the percentage tumor nuclei and tumor annotation for manual macrodissection. In this study on NSCLC, we demonstrate considerable variation in tumor nuclei percentage between pathologists, potentially undermining the precision of NSCLC molecular evaluation and emphasising the need for quantitative tumor evaluation. We subsequently describe the development and validation of a system called TissueMark for automated tumor annotation and percentage tumor nuclei measurement in NSCLC using computerized image analysis. Evaluation of 245 NSCLC slides showed precise automated tumor annotation of cases using Tissuemark, strong concordance with manually drawn boundaries and identical EGFR mutational status, following manual macrodissection from the image analysis generated tumor boundaries. Automated analysis of cell counts for % tumor measurements by Tissuemark showed reduced variability and significant correlation (p < 0.001) with benchmark tumor cell counts. This study demonstrates a robust image analysis technology that can facilitate the automated quantitative analysis of tissue samples for molecular profiling in discovery and diagnostics. Impact Journals LLC 2015-08-03 /pmc/articles/PMC4695036/ /pubmed/26317646 Text en Copyright: © 2015 Hamilton et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Hamilton, Peter W.
Wang, Yinhai
Boyd, Clinton
James, Jacqueline A.
Loughrey, Maurice B.
Hougton, Joseph P.
Boyle, David P.
Kelly, Paul
Maxwell, Perry
McCleary, David
Diamond, James
McArt, Darragh G.
Tunstall, Jonathon
Bankhead, Peter
Salto-Tellez, Manuel
Automated tumor analysis for molecular profiling in lung cancer
title Automated tumor analysis for molecular profiling in lung cancer
title_full Automated tumor analysis for molecular profiling in lung cancer
title_fullStr Automated tumor analysis for molecular profiling in lung cancer
title_full_unstemmed Automated tumor analysis for molecular profiling in lung cancer
title_short Automated tumor analysis for molecular profiling in lung cancer
title_sort automated tumor analysis for molecular profiling in lung cancer
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4695036/
https://www.ncbi.nlm.nih.gov/pubmed/26317646
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