文献类型: 会议论文
第一作者: Peter D. Erickson
作者: Peter D. Erickson 1 ; Tejas Sudharshan Mathai 1 ; Ronald M. Summers 1 ;
作者机构: 1.Imaging Biomarkers and Computer-Aided Diagnosis Laboratory, Radiology and Imaging Sciences, Clinical Center, National Institutes of Health
关键词: CT;Universal lesion detection;Class imbalance;Deep learning;DeepLesion
会议名称: International Workshop on Medical Image Learning with Limited and Noisy Data
主办单位:
页码: 177-186
摘要: Radiologists routinely detect and size lesions in CT to stage cancer and assess tumor burden. To potentially aid their efforts, multiple lesion detection algorithms have been developed with a large public dataset called DeepLesion (32,735 lesions, 32,120 CT slices, 10,594 studies, 4,427 patients, 8 body part labels). However, this dataset contains missing measurements and lesion tags, and exhibits a severe imbalance in the number of lesions per label category. In this work, we utilize a limited subset of DeepLesion (6%, 1331 lesions, 1309 slices) containing lesion annotations and body part label tags to train a VFNet model to detect lesions and tag them. We address the class imbalance by conducting three experiments: 1) Balancing data by the body part labels, 2) Balancing data by the number of lesions per patient, and 3) Balancing data by the lesion size. In contrast to a randomly sampled (unbalanced) data subset, our results indicated that balancing the body part labels always increased sensitivity for lesions ≥ 1 cm for classes with low data quantities (Bone: 80% vs. 46%, Kidney: 77% vs. 61%, Soft Tissue: 70% vs. 60%, Pelvis: 83% vs. 76%). Similar trends were seen for three other models tested (FasterRCNN, RetinaNet, FoveaBox). Balancing data by lesion size also helped the VFNet model improve recalls for all classes in contrast to an unbalanced dataset. We also provide a structured reporting guideline for a "Lesions" subsection to be entered into the "Findings" section of a radiology report. To our knowledge, we are the first to report the class imbalance in DeepLesion, and have taken data-driven steps to address it in the context of joint lesion detection and tagging.
分类号: tp391.41-53
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