Evidence map›Paper›PMID 34320986›Full record

ArticleBiomedical engineering online2021

Classification of microcalcification clusters in digital breast tomosynthesis using ensemble convolutional neural network.

Bingbing Xiao, Haotian Sun, You Meng, Yunsong Peng, Xiaodong Yang, Shuangqing Chen, Zhuangzhi Yan, Jian Zheng

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Article in Biomedical engineering online, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

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10citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

10 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Bingbing Xiao *Institute of Biomedical Engineering, School of Communication and Information Engineering, Shanghai University, Shanghai, China.
Haotian Sun *University of Science and Technology of China, Hefei, China.
You MengDepartment of Breast Surgery, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou, China.
Yunsong PengUniversity of Science and Technology of China, Hefei, China.
Xiaodong YangDepartment of Medical Imaging, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, China.
Shuangqing ChenGusu School, Nanjing Medical University, Suzhou, China. sznaonao@163.com.
Zhuangzhi YanInstitute of Biomedical Engineering, School of Communication and Information Engineering, Shanghai University, Shanghai, China. zzyan@shu.edu.cn.
Jian ZhengDepartment of Medical Imaging, Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, China. zhengj@sibet.ac.cn.

Funding

Applied Basic Research Project in Suzhou sys2018083The Research Project of Gusu School of Nanjing Medical University GSKY20210227
6 · The paper itself

Abstract

backgroundThe classification of benign and malignant microcalcification clusters (MCs) is an important task for computer-aided diagnosis (CAD) of digital breast tomosynthesis (DBT) images. Influenced by imaging method, DBT has the characteristic of anisotropic resolution, in which the resolution of intra-slice and inter-slice is quite different. In addition, the sharpness of MCs in different slices of DBT is quite different, among which the clearest slice is called focus slice. These characteristics limit the performance of CAD algorithms based on standard 3D convolution neural network (CNN).

methodsTo make full use of the characteristics of the DBT, we proposed a new ensemble CNN, which consists of the 2D ResNet34 and the anisotropic 3D ResNet to extract the 2D focus slice features and 3D contextual features of MCs, respectively. Moreover, the anisotropic 3D convolution is used to build 3D ResNet to avoid the influence of DBT anisotropy.

resultsThe proposed method was evaluated on 495 MCs in DBT images of 275 patients, which are collected from our collaborative hospital. The area under the curve (AUC) of receiver operating characteristic (ROC) and accuracy of classifying benign and malignant MCs using decision-level ensemble strategy were 0.8837 and 82.00%, which were significantly higher than the experimental results of 2D ResNet34 (AUC: 0.8264, ACC: 76.00%) and anisotropic 3D ResNet (AUC: 0.8455, ACC: 76.00%). Compared with the results of 3D features classification in the radiomics, the AUC of the deep learning method with decision-level ensemble strategy was improved by 0.0435, and the F1 score was improved from 79.37 to 85.71%. More importantly, the sensitivity increased from 78.13 to 84.38%, and the specificity increased from 66.67 to 77.78%, which effectively reduced the false positives of diagnosis

conclusionThe results fully prove that the ensemble CNN can effectively integrate 2D features and 3D features, improve the classification performance of benign and malignant MCs in DBT, and reduce the false positives.

Indexed as

Breast NeoplasmsCalcinosisDiagnosis, Computer-AssistedFemaleHumansMammographyNeural Networks, ComputerROC CurveClassificationConvolution neural networkDigital breast tomosynthesisEnsemble learningMicrocalcification cluster

Identifiers

PMID34320986
PMCPMC8317331

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