TY - GEN
T1 - Human ability enhancement for reading mammographic masses by a deep learning technique
AU - Homma, Noriyasu
AU - Noro, Kyohei
AU - Zhang, Xiaoyong
AU - Kon, Yutaro
AU - Ichiji, Kei
AU - Bukovsky, Ivo
AU - Sato, Akiko
AU - Mori, Naoko
N1 - Funding Information:
ACKNOWLEDGMENT This work was partially supported by Smart Aging Research Center, Tohoku University, and JSPS KAKENHI Grant Numbers JP18K19892, JP19H04479, and 20K08012.
Publisher Copyright:
© 2020 IEEE.
PY - 2020/12/16
Y1 - 2020/12/16
N2 - The usefulness of taking mammography has widely been recognized, but screening mammography occasionally results in an excessive recommendation for subsequent biopsy causing many women inconvenience and severe anxiety. Especially, there is a high chance of unnecessary biopsy recommendation for those findings which are difficult to be classified into malignancy and benignancy. However, few have focused on the computer-aided diagnosis (CAD) performance for such difficult cases. To address this problem, we developed a deep learning based classification technique to aid the difficult diagnosis. We evaluated 100 benign and malignant masses of the breast imaging-reporting and data system (BI-RADS) Category 4 that are generally difficult to be classified into malignant and benign. Five certificated doctors participated in the experiments where each doctor reads the 100 images alone first and a week later reads again with the proposed CAD system. The area under the receiver operating characteristic curve (AUC-ROC) for the CAD system was 0.79. This is greater than 0.65, the average value of the human readers' AUC-ROCs, while the average value of the human readers' AUC-ROCs reached the best value of 0.8 when they used the CAD system. These results suggest that the proposed CAD system is able to not only outperform human readers in classifying the masses, but also enhance the human performance in this difficult task.
AB - The usefulness of taking mammography has widely been recognized, but screening mammography occasionally results in an excessive recommendation for subsequent biopsy causing many women inconvenience and severe anxiety. Especially, there is a high chance of unnecessary biopsy recommendation for those findings which are difficult to be classified into malignancy and benignancy. However, few have focused on the computer-aided diagnosis (CAD) performance for such difficult cases. To address this problem, we developed a deep learning based classification technique to aid the difficult diagnosis. We evaluated 100 benign and malignant masses of the breast imaging-reporting and data system (BI-RADS) Category 4 that are generally difficult to be classified into malignant and benign. Five certificated doctors participated in the experiments where each doctor reads the 100 images alone first and a week later reads again with the proposed CAD system. The area under the receiver operating characteristic curve (AUC-ROC) for the CAD system was 0.79. This is greater than 0.65, the average value of the human readers' AUC-ROCs, while the average value of the human readers' AUC-ROCs reached the best value of 0.8 when they used the CAD system. These results suggest that the proposed CAD system is able to not only outperform human readers in classifying the masses, but also enhance the human performance in this difficult task.
KW - and deep learning
KW - breast cancer
KW - computer aided diagnosis
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U2 - 10.1109/BIBM49941.2020.9313564
DO - 10.1109/BIBM49941.2020.9313564
M3 - Conference contribution
AN - SCOPUS:85100356680
T3 - Proceedings - 2020 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2020
SP - 2962
EP - 2964
BT - Proceedings - 2020 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2020
A2 - Park, Taesung
A2 - Cho, Young-Rae
A2 - Hu, Xiaohua Tony
A2 - Yoo, Illhoi
A2 - Woo, Hyun Goo
A2 - Wang, Jianxin
A2 - Facelli, Julio
A2 - Nam, Seungyoon
A2 - Kang, Mingon
PB - Institute of Electrical and Electronics Engineers Inc.
T2 - 2020 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2020
Y2 - 16 December 2020 through 19 December 2020
ER -