卷积神经网络
深度学习
医学
模式治疗法
人工智能
肝肿瘤
代表(政治)
模式识别(心理学)
放射科
计算机科学
病理
内科学
肝细胞癌
政治
政治学
法学
作者
Masaya Sato,Tamaki Kobayashi,Yoko Soroida,Takashi Tanaka,T. Nakatsuka,Hayato Nakagawa,Ayaka Nakamura,M. Kurihara,Momoe Endo,Hiromi Hikita,Mamiko Sato,Hiroaki Gotoh,Tomomi Iwai,Ryosuke Tateishi,Kazuhiko Koike,Yutaka Yatomi
摘要
Abstract Background and Aim Recently, multimodal representation learning for images and other information such as numbers or language has gained much attention. The aim of the current study was to analyze the diagnostic performance of deep multimodal representation model‐based integration of tumor image, patient background, and blood biomarkers for the differentiation of liver tumors observed using B‐mode ultrasonography (US). Method First, we applied supervised learning with a convolutional neural network (CNN) to 972 liver nodules in the training and development sets to develop a predictive model using segmented B‐mode tumor images. Additionally, we also applied a deep multimodal representation model to integrate information about patient background or blood biomarkers to B‐mode images. We then investigated the performance of the models in an independent test set of 108 liver nodules. Results Using only the segmented B‐mode images, the diagnostic accuracy and area under the curve (AUC) values were 68.52% and 0.721, respectively. As the information about patient background and blood biomarkers was integrated, the diagnostic performance increased in a stepwise manner. The diagnostic accuracy and AUC value of the multimodal DL model (which integrated B‐mode tumor image, patient age, sex, aspartate aminotransferase, alanine aminotransferase, platelet count, and albumin data) reached 96.30% and 0.994, respectively. Conclusion Integration of patient background and blood biomarkers in addition to US image using multimodal representation learning outperformed the CNN model using US images. We expect that the deep multimodal representation model could be a feasible and acceptable tool for the definitive diagnosis of liver tumors using B‐mode US.
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