Cargando…

Artificial Intelligence-based Tumor Segmentation in Mouse Models of Lung Adenocarcinoma

BACKGROUND: Mouse models are highly effective for studying the pathophysiology of lung adenocarcinoma and evaluating new treatment strategies. Treatment efficacy is primarily determined by the total tumor burden measured on excised tumor specimens. The measurement process is time-consuming and prone...

Descripción completa

Detalles Bibliográficos
Autores principales: Arlova, Alena, Jin, Chengcheng, Wong-Rolle, Abigail, Chen, Eric S., Lisle, Curtis, Brown, G. Thomas, Lay, Nathan, Choyke, Peter L., Turkbey, Baris, Harmon, Stephanie, Zhao, Chen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860735/
https://www.ncbi.nlm.nih.gov/pubmed/35242446
http://dx.doi.org/10.1016/j.jpi.2022.100007
_version_ 1784654737984978944
author Arlova, Alena
Jin, Chengcheng
Wong-Rolle, Abigail
Chen, Eric S.
Lisle, Curtis
Brown, G. Thomas
Lay, Nathan
Choyke, Peter L.
Turkbey, Baris
Harmon, Stephanie
Zhao, Chen
author_facet Arlova, Alena
Jin, Chengcheng
Wong-Rolle, Abigail
Chen, Eric S.
Lisle, Curtis
Brown, G. Thomas
Lay, Nathan
Choyke, Peter L.
Turkbey, Baris
Harmon, Stephanie
Zhao, Chen
author_sort Arlova, Alena
collection PubMed
description BACKGROUND: Mouse models are highly effective for studying the pathophysiology of lung adenocarcinoma and evaluating new treatment strategies. Treatment efficacy is primarily determined by the total tumor burden measured on excised tumor specimens. The measurement process is time-consuming and prone to human errors. To address this issue, we developed a novel deep learning model to segment lung tumor foci on digitally scanned hematoxylin and eosin (H&E) histology slides. METHODS: Digital slides of 239 mice from 9 experimental cohorts were split into training (n=137), validation (n=37), and testing cohorts (n=65). Image patches of 500×500 pixels were extracted from 5× and 10× magnifications, along with binary masks of expert annotations representing ground-truth tumor regions. Deep learning models utilizing DeepLabV3+ and UNet architectures were trained for binary segmentation of tumor foci under varying stain normalization conditions. The performance of algorithm segmentation was assessed by Dice Coefficient, and detection was evaluated by sensitivity and positive-predictive value (PPV). RESULTS: The best model on patch-based validation was DeepLabV3+ using a Resnet-50 backbone, which achieved Dice 0.890 and 0.873 on validation and testing cohort, respectively. This result corresponded to 91.3 Sensitivity and 51.0 PPV in the validation cohort and 93.7 Sensitivity and 51.4 PPV in the testing cohort. False positives could be reduced 10-fold with thresholding artificial intelligence (AI) predicted output by area, without negative impact on Dice Coefficient. Evaluation at various stain normalization strategies did not demonstrate improvement from the baseline model. CONCLUSIONS: A robust AI-based algorithm for detecting and segmenting lung tumor foci in the pre-clinical mouse models was developed. The output of this algorithm is compatible with open-source software that researchers commonly use.
format Online
Article
Text
id pubmed-8860735
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-88607352022-03-02 Artificial Intelligence-based Tumor Segmentation in Mouse Models of Lung Adenocarcinoma Arlova, Alena Jin, Chengcheng Wong-Rolle, Abigail Chen, Eric S. Lisle, Curtis Brown, G. Thomas Lay, Nathan Choyke, Peter L. Turkbey, Baris Harmon, Stephanie Zhao, Chen J Pathol Inform Original Research Article BACKGROUND: Mouse models are highly effective for studying the pathophysiology of lung adenocarcinoma and evaluating new treatment strategies. Treatment efficacy is primarily determined by the total tumor burden measured on excised tumor specimens. The measurement process is time-consuming and prone to human errors. To address this issue, we developed a novel deep learning model to segment lung tumor foci on digitally scanned hematoxylin and eosin (H&E) histology slides. METHODS: Digital slides of 239 mice from 9 experimental cohorts were split into training (n=137), validation (n=37), and testing cohorts (n=65). Image patches of 500×500 pixels were extracted from 5× and 10× magnifications, along with binary masks of expert annotations representing ground-truth tumor regions. Deep learning models utilizing DeepLabV3+ and UNet architectures were trained for binary segmentation of tumor foci under varying stain normalization conditions. The performance of algorithm segmentation was assessed by Dice Coefficient, and detection was evaluated by sensitivity and positive-predictive value (PPV). RESULTS: The best model on patch-based validation was DeepLabV3+ using a Resnet-50 backbone, which achieved Dice 0.890 and 0.873 on validation and testing cohort, respectively. This result corresponded to 91.3 Sensitivity and 51.0 PPV in the validation cohort and 93.7 Sensitivity and 51.4 PPV in the testing cohort. False positives could be reduced 10-fold with thresholding artificial intelligence (AI) predicted output by area, without negative impact on Dice Coefficient. Evaluation at various stain normalization strategies did not demonstrate improvement from the baseline model. CONCLUSIONS: A robust AI-based algorithm for detecting and segmenting lung tumor foci in the pre-clinical mouse models was developed. The output of this algorithm is compatible with open-source software that researchers commonly use. Elsevier 2022-01-20 /pmc/articles/PMC8860735/ /pubmed/35242446 http://dx.doi.org/10.1016/j.jpi.2022.100007 Text en © 2022 Published by Elsevier Inc. on behalf of Association for Pathology Informatics. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research Article
Arlova, Alena
Jin, Chengcheng
Wong-Rolle, Abigail
Chen, Eric S.
Lisle, Curtis
Brown, G. Thomas
Lay, Nathan
Choyke, Peter L.
Turkbey, Baris
Harmon, Stephanie
Zhao, Chen
Artificial Intelligence-based Tumor Segmentation in Mouse Models of Lung Adenocarcinoma
title Artificial Intelligence-based Tumor Segmentation in Mouse Models of Lung Adenocarcinoma
title_full Artificial Intelligence-based Tumor Segmentation in Mouse Models of Lung Adenocarcinoma
title_fullStr Artificial Intelligence-based Tumor Segmentation in Mouse Models of Lung Adenocarcinoma
title_full_unstemmed Artificial Intelligence-based Tumor Segmentation in Mouse Models of Lung Adenocarcinoma
title_short Artificial Intelligence-based Tumor Segmentation in Mouse Models of Lung Adenocarcinoma
title_sort artificial intelligence-based tumor segmentation in mouse models of lung adenocarcinoma
topic Original Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8860735/
https://www.ncbi.nlm.nih.gov/pubmed/35242446
http://dx.doi.org/10.1016/j.jpi.2022.100007
work_keys_str_mv AT arlovaalena artificialintelligencebasedtumorsegmentationinmousemodelsoflungadenocarcinoma
AT jinchengcheng artificialintelligencebasedtumorsegmentationinmousemodelsoflungadenocarcinoma
AT wongrolleabigail artificialintelligencebasedtumorsegmentationinmousemodelsoflungadenocarcinoma
AT chenerics artificialintelligencebasedtumorsegmentationinmousemodelsoflungadenocarcinoma
AT lislecurtis artificialintelligencebasedtumorsegmentationinmousemodelsoflungadenocarcinoma
AT browngthomas artificialintelligencebasedtumorsegmentationinmousemodelsoflungadenocarcinoma
AT laynathan artificialintelligencebasedtumorsegmentationinmousemodelsoflungadenocarcinoma
AT choykepeterl artificialintelligencebasedtumorsegmentationinmousemodelsoflungadenocarcinoma
AT turkbeybaris artificialintelligencebasedtumorsegmentationinmousemodelsoflungadenocarcinoma
AT harmonstephanie artificialintelligencebasedtumorsegmentationinmousemodelsoflungadenocarcinoma
AT zhaochen artificialintelligencebasedtumorsegmentationinmousemodelsoflungadenocarcinoma