Computer-assisted diagnosis of early esophageal squamous cell carcinoma using narrow-band imaging magnifying endoscopy

被引:87
|
作者
Zhao, Yuan-Yuan [1 ]
Xue, Di-Xiu [2 ]
Wang, Ya-Lei [1 ]
Zhang, Rong [3 ]
Sun, Bin [1 ]
Cai, Yong-Ping [4 ]
Feng, Hui [1 ]
Cai, Yi [1 ]
Xu, Jian-Ming [1 ]
机构
[1] Anhui Med Univ, Dept Gastroenterol, Affiliated Hosp 1, Jixi Rd 218, Hefei 230022, Anhui, Peoples R China
[2] Univ Sci & Technol China, Dept Elect Engn & Informat Sci, Hefei, Anhui, Peoples R China
[3] Chinese Acad Sci, Key Lab Electromagnet Space Informat, Hefei, Anhui, Peoples R China
[4] Anhui Med Univ, Affiliated Hosp 1, Dept Pathol, Hefei, Anhui, Peoples R China
关键词
AIDED DIAGNOSIS; LESIONS; CLASSIFICATION; SYSTEM;
D O I
10.1055/a-0756-8754
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background We developed a computer-assisted diagnosis model to evaluate the feasibility of automated classification of intrapapillary capillary loops (IPCLs) to improve the detection of esophageal squamous cell carcinoma (ESCC). Methods We recruited patients who underwent magnifying endoscopy with narrow-band imaging for evaluation of a suspicious esophageal condition. Case images were evaluated to establish a gold standard IPCL classification according to the endoscopic diagnosis and histological findings. A double-labeling fully convolutional network (FCN) was developed for image segmentation. Diagnostic performance of the model was compared with that of endoscopists grouped according to years of experience (senior >15 years; mid level 10-15 years; junior 5-10 years). Results Of the 1383 lesions in the study, the mean accuracies of IPCL classification were 92.0%, 82.0%, and 73.3%, for the senior, mid level, and junior groups, respectively. The mean diagnostic accuracy of the model was 89.2% and 93.0% at the lesion and pixel levels, respectively. The interobserver agreement between the model and the gold standard was substantial (kappa value, 0.719). The accuracy of the model for inflammatory lesions (92.5%) was superior to that of the mid level (88.1%) and junior (86.3%) groups ( P <0.001). For malignant lesions, the accuracy of the model (B1, 87.6%; B2, 93.9%) was significantly higher than that of the mid level (B1, 79.1%; B2, 90.0%) and junior (B1, 69.2%; B2, 79.3%) groups ( P <0.001). Conclusions Double-labeling FCN automated IPCL recognition was feasible and could facilitate early detection of ESCC.
引用
收藏
页码:333 / 341
页数:9
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