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Leveraging artificial intelligence to predict ERG gene fusion status in prostate cancer

BACKGROUND: TMPRSS2-ERG gene rearrangement, the most common E26 transformation specific (ETS) gene fusion within prostate cancer, is known to contribute to the pathogenesis of this disease and carries diagnostic annotations for prostate cancer patients clinically. The ERG rearrangement status in pro...

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Autores principales: Dadhania, Vipulkumar, Gonzalez, Daniel, Yousif, Mustafa, Cheng, Jerome, Morgan, Todd M., Spratt, Daniel E., Reichert, Zachery R., Mannan, Rahul, Wang, Xiaoming, Chinnaiyan, Anya, Cao, Xuhong, Dhanasekaran, Saravana M., Chinnaiyan, Arul M., Pantanowitz, Liron, Mehra, Rohit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069768/
https://www.ncbi.nlm.nih.gov/pubmed/35513774
http://dx.doi.org/10.1186/s12885-022-09559-4
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author Dadhania, Vipulkumar
Gonzalez, Daniel
Yousif, Mustafa
Cheng, Jerome
Morgan, Todd M.
Spratt, Daniel E.
Reichert, Zachery R.
Mannan, Rahul
Wang, Xiaoming
Chinnaiyan, Anya
Cao, Xuhong
Dhanasekaran, Saravana M.
Chinnaiyan, Arul M.
Pantanowitz, Liron
Mehra, Rohit
author_facet Dadhania, Vipulkumar
Gonzalez, Daniel
Yousif, Mustafa
Cheng, Jerome
Morgan, Todd M.
Spratt, Daniel E.
Reichert, Zachery R.
Mannan, Rahul
Wang, Xiaoming
Chinnaiyan, Anya
Cao, Xuhong
Dhanasekaran, Saravana M.
Chinnaiyan, Arul M.
Pantanowitz, Liron
Mehra, Rohit
author_sort Dadhania, Vipulkumar
collection PubMed
description BACKGROUND: TMPRSS2-ERG gene rearrangement, the most common E26 transformation specific (ETS) gene fusion within prostate cancer, is known to contribute to the pathogenesis of this disease and carries diagnostic annotations for prostate cancer patients clinically. The ERG rearrangement status in prostatic adenocarcinoma currently cannot be reliably identified from histologic features on H&E-stained slides alone and hence requires ancillary studies such as immunohistochemistry (IHC), fluorescent in situ hybridization (FISH) or next generation sequencing (NGS) for identification. METHODS: OBJECTIVE: We accordingly sought to develop a deep learning-based algorithm to identify ERG rearrangement status in prostatic adenocarcinoma based on digitized slides of H&E morphology alone. DESIGN: Setting, and Participants: Whole slide images from 392 in-house and TCGA cases were employed and annotated using QuPath. Image patches of 224 × 224 pixel were exported at 10 ×, 20 ×, and 40 × for input into a deep learning model based on MobileNetV2 convolutional neural network architecture pre-trained on ImageNet. A separate model was trained for each magnification. Training and test datasets consisted of 261 cases and 131 cases, respectively. The output of the model included a prediction of ERG-positive (ERG rearranged) or ERG-negative (ERG not rearranged) status for each input patch. Outcome measurements and statistical analysis: Various accuracy measurements including area under the curve (AUC) of the receiver operating characteristic (ROC) curves were used to evaluate the deep learning model. RESULTS AND LIMITATIONS: All models showed similar ROC curves with AUC results ranging between 0.82 and 0.85. The sensitivity and specificity of these models were 75.0% and 83.1% (20 × model), respectively. CONCLUSIONS: A deep learning-based model can successfully predict ERG rearrangement status in the majority of prostatic adenocarcinomas utilizing only H&E-stained digital slides. Such an artificial intelligence-based model can eliminate the need for using extra tumor tissue to perform ancillary studies in order to assess for ERG gene rearrangement in prostatic adenocarcinoma.
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spelling pubmed-90697682022-05-05 Leveraging artificial intelligence to predict ERG gene fusion status in prostate cancer Dadhania, Vipulkumar Gonzalez, Daniel Yousif, Mustafa Cheng, Jerome Morgan, Todd M. Spratt, Daniel E. Reichert, Zachery R. Mannan, Rahul Wang, Xiaoming Chinnaiyan, Anya Cao, Xuhong Dhanasekaran, Saravana M. Chinnaiyan, Arul M. Pantanowitz, Liron Mehra, Rohit BMC Cancer Research Article BACKGROUND: TMPRSS2-ERG gene rearrangement, the most common E26 transformation specific (ETS) gene fusion within prostate cancer, is known to contribute to the pathogenesis of this disease and carries diagnostic annotations for prostate cancer patients clinically. The ERG rearrangement status in prostatic adenocarcinoma currently cannot be reliably identified from histologic features on H&E-stained slides alone and hence requires ancillary studies such as immunohistochemistry (IHC), fluorescent in situ hybridization (FISH) or next generation sequencing (NGS) for identification. METHODS: OBJECTIVE: We accordingly sought to develop a deep learning-based algorithm to identify ERG rearrangement status in prostatic adenocarcinoma based on digitized slides of H&E morphology alone. DESIGN: Setting, and Participants: Whole slide images from 392 in-house and TCGA cases were employed and annotated using QuPath. Image patches of 224 × 224 pixel were exported at 10 ×, 20 ×, and 40 × for input into a deep learning model based on MobileNetV2 convolutional neural network architecture pre-trained on ImageNet. A separate model was trained for each magnification. Training and test datasets consisted of 261 cases and 131 cases, respectively. The output of the model included a prediction of ERG-positive (ERG rearranged) or ERG-negative (ERG not rearranged) status for each input patch. Outcome measurements and statistical analysis: Various accuracy measurements including area under the curve (AUC) of the receiver operating characteristic (ROC) curves were used to evaluate the deep learning model. RESULTS AND LIMITATIONS: All models showed similar ROC curves with AUC results ranging between 0.82 and 0.85. The sensitivity and specificity of these models were 75.0% and 83.1% (20 × model), respectively. CONCLUSIONS: A deep learning-based model can successfully predict ERG rearrangement status in the majority of prostatic adenocarcinomas utilizing only H&E-stained digital slides. Such an artificial intelligence-based model can eliminate the need for using extra tumor tissue to perform ancillary studies in order to assess for ERG gene rearrangement in prostatic adenocarcinoma. BioMed Central 2022-05-05 /pmc/articles/PMC9069768/ /pubmed/35513774 http://dx.doi.org/10.1186/s12885-022-09559-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Dadhania, Vipulkumar
Gonzalez, Daniel
Yousif, Mustafa
Cheng, Jerome
Morgan, Todd M.
Spratt, Daniel E.
Reichert, Zachery R.
Mannan, Rahul
Wang, Xiaoming
Chinnaiyan, Anya
Cao, Xuhong
Dhanasekaran, Saravana M.
Chinnaiyan, Arul M.
Pantanowitz, Liron
Mehra, Rohit
Leveraging artificial intelligence to predict ERG gene fusion status in prostate cancer
title Leveraging artificial intelligence to predict ERG gene fusion status in prostate cancer
title_full Leveraging artificial intelligence to predict ERG gene fusion status in prostate cancer
title_fullStr Leveraging artificial intelligence to predict ERG gene fusion status in prostate cancer
title_full_unstemmed Leveraging artificial intelligence to predict ERG gene fusion status in prostate cancer
title_short Leveraging artificial intelligence to predict ERG gene fusion status in prostate cancer
title_sort leveraging artificial intelligence to predict erg gene fusion status in prostate cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9069768/
https://www.ncbi.nlm.nih.gov/pubmed/35513774
http://dx.doi.org/10.1186/s12885-022-09559-4
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