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Application of deep learning to identify ductal carcinoma in situ and microinvasion of the breast using ultrasound imaging

BACKGROUND: The treatment and prognosis of breast ductal carcinoma in situ (DCIS) with and without microinvasion (MIC) are different. Ultrasound imaging shows that DCIS is a heterogeneous breast tumor with diverse manifestations. DCIS means that the cancer cells are confined in the duct without pene...

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Autores principales: Zhu, Meng, Pi, Yong, Jiang, Zekun, Wu, Yanyan, Bu, Hong, Bao, Ji, Chen, Yujuan, Zhao, Lijun, Peng, Yulan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403599/
https://www.ncbi.nlm.nih.gov/pubmed/36060588
http://dx.doi.org/10.21037/qims-22-46
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author Zhu, Meng
Pi, Yong
Jiang, Zekun
Wu, Yanyan
Bu, Hong
Bao, Ji
Chen, Yujuan
Zhao, Lijun
Peng, Yulan
author_facet Zhu, Meng
Pi, Yong
Jiang, Zekun
Wu, Yanyan
Bu, Hong
Bao, Ji
Chen, Yujuan
Zhao, Lijun
Peng, Yulan
author_sort Zhu, Meng
collection PubMed
description BACKGROUND: The treatment and prognosis of breast ductal carcinoma in situ (DCIS) with and without microinvasion (MIC) are different. Ultrasound imaging shows that DCIS is a heterogeneous breast tumor with diverse manifestations. DCIS means that the cancer cells are confined in the duct without penetrating the basement membrane, MIC means that the cancer cells penetrate the basement membrane and the maximum diameter of any largest invasive lesion is less than or equal to 1 mm. This study was designed to evaluate how deep learning can be used to identify DCIS with MIC on ultrasound images. METHODS: The clinical and ultrasound data of 467 consecutive inpatients diagnosed with DCIS (213 with MIC) in West China Hospital of Sichuan University were collected from January 2013 to April 2019 and randomly apportioned to training and internal validation sets. An external validation set comprised data from Sichuan Provincial People's Hospital with 101 patients (33 with MIC) collected between January 2017 and December 2019. There were 2,492 original images; 66% of these were used to establish a model, and the remaining 34% were used to evaluate the model. Three experienced breast ultrasound clinicians analyzed the ultrasound images to establish a logistic regression model. Finally, the logistic regression model and five deep learning models (ResNet-50, ResNet-101, DenseNet-161, DenseNet-169, and Inception-v3) were compared and evaluated to assess their diagnostic efficiency when identifying MIC based on ultrasound image data. RESULTS: The characteristics of high nuclear grade (P<0.001), necrosis (P=0.006), estrogen receptor negative (ER(−); P=0.003), progesterone receptor negative (PR(−); P=0.001), human epidermal growth factor receptor 2 positive (HER2+; P=0.034), lymphatic metastasis (P=0.008), and calcification (P<0.001) all showed significant correlations with MIC. The Inception-v3 model achieved the best performance (P<0.05) in MIC identification. The area under the receiver operating curve (AUC) of the Inception-v3 model was 0.803 [95% confidence interval (CI): 0.709 to 0.878], with a classification accuracy of 0.766, a sensitivity of 0.767, and a specificity of 0.765. CONCLUSIONS: Deep learning can be used to identify MIC of breast DCIS from ultrasound images. Models based on Inception-v3 can provide automated detection of DCIS with MIC from ultrasound images.
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spelling pubmed-94035992022-09-01 Application of deep learning to identify ductal carcinoma in situ and microinvasion of the breast using ultrasound imaging Zhu, Meng Pi, Yong Jiang, Zekun Wu, Yanyan Bu, Hong Bao, Ji Chen, Yujuan Zhao, Lijun Peng, Yulan Quant Imaging Med Surg Original Article BACKGROUND: The treatment and prognosis of breast ductal carcinoma in situ (DCIS) with and without microinvasion (MIC) are different. Ultrasound imaging shows that DCIS is a heterogeneous breast tumor with diverse manifestations. DCIS means that the cancer cells are confined in the duct without penetrating the basement membrane, MIC means that the cancer cells penetrate the basement membrane and the maximum diameter of any largest invasive lesion is less than or equal to 1 mm. This study was designed to evaluate how deep learning can be used to identify DCIS with MIC on ultrasound images. METHODS: The clinical and ultrasound data of 467 consecutive inpatients diagnosed with DCIS (213 with MIC) in West China Hospital of Sichuan University were collected from January 2013 to April 2019 and randomly apportioned to training and internal validation sets. An external validation set comprised data from Sichuan Provincial People's Hospital with 101 patients (33 with MIC) collected between January 2017 and December 2019. There were 2,492 original images; 66% of these were used to establish a model, and the remaining 34% were used to evaluate the model. Three experienced breast ultrasound clinicians analyzed the ultrasound images to establish a logistic regression model. Finally, the logistic regression model and five deep learning models (ResNet-50, ResNet-101, DenseNet-161, DenseNet-169, and Inception-v3) were compared and evaluated to assess their diagnostic efficiency when identifying MIC based on ultrasound image data. RESULTS: The characteristics of high nuclear grade (P<0.001), necrosis (P=0.006), estrogen receptor negative (ER(−); P=0.003), progesterone receptor negative (PR(−); P=0.001), human epidermal growth factor receptor 2 positive (HER2+; P=0.034), lymphatic metastasis (P=0.008), and calcification (P<0.001) all showed significant correlations with MIC. The Inception-v3 model achieved the best performance (P<0.05) in MIC identification. The area under the receiver operating curve (AUC) of the Inception-v3 model was 0.803 [95% confidence interval (CI): 0.709 to 0.878], with a classification accuracy of 0.766, a sensitivity of 0.767, and a specificity of 0.765. CONCLUSIONS: Deep learning can be used to identify MIC of breast DCIS from ultrasound images. Models based on Inception-v3 can provide automated detection of DCIS with MIC from ultrasound images. AME Publishing Company 2022-09 /pmc/articles/PMC9403599/ /pubmed/36060588 http://dx.doi.org/10.21037/qims-22-46 Text en 2022 Quantitative Imaging in Medicine and Surgery. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Zhu, Meng
Pi, Yong
Jiang, Zekun
Wu, Yanyan
Bu, Hong
Bao, Ji
Chen, Yujuan
Zhao, Lijun
Peng, Yulan
Application of deep learning to identify ductal carcinoma in situ and microinvasion of the breast using ultrasound imaging
title Application of deep learning to identify ductal carcinoma in situ and microinvasion of the breast using ultrasound imaging
title_full Application of deep learning to identify ductal carcinoma in situ and microinvasion of the breast using ultrasound imaging
title_fullStr Application of deep learning to identify ductal carcinoma in situ and microinvasion of the breast using ultrasound imaging
title_full_unstemmed Application of deep learning to identify ductal carcinoma in situ and microinvasion of the breast using ultrasound imaging
title_short Application of deep learning to identify ductal carcinoma in situ and microinvasion of the breast using ultrasound imaging
title_sort application of deep learning to identify ductal carcinoma in situ and microinvasion of the breast using ultrasound imaging
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403599/
https://www.ncbi.nlm.nih.gov/pubmed/36060588
http://dx.doi.org/10.21037/qims-22-46
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