CVMay 28, 2020

Universal Lesion Detection by Learning from Multiple Heterogeneously Labeled Datasets

arXiv:2005.13753v118 citations
AI Analysis

This work addresses the challenge of detecting diverse lesions in clinical radiology, which is crucial for comprehensive medical diagnosis, but it is incremental as it builds on existing datasets and methods.

The paper tackles the problem of universal lesion detection (ULD) in medical imaging by leveraging multiple heterogeneously labeled datasets, including DeepLesion and single-type datasets like LUNA and LiTS, to improve detection of various lesion types across the body. The proposed framework, which includes multi-task learning, embedding matching for missing annotations, and knowledge transfer, outperforms the state-of-the-art by 29% in average sensitivity on a fully annotated subset of DeepLesion.

Lesion detection is an important problem within medical imaging analysis. Most previous work focuses on detecting and segmenting a specialized category of lesions (e.g., lung nodules). However, in clinical practice, radiologists are responsible for finding all possible types of anomalies. The task of universal lesion detection (ULD) was proposed to address this challenge by detecting a large variety of lesions from the whole body. There are multiple heterogeneously labeled datasets with varying label completeness: DeepLesion, the largest dataset of 32,735 annotated lesions of various types, but with even more missing annotation instances; and several fully-labeled single-type lesion datasets, such as LUNA for lung nodules and LiTS for liver tumors. In this work, we propose a novel framework to leverage all these datasets together to improve the performance of ULD. First, we learn a multi-head multi-task lesion detector using all datasets and generate lesion proposals on DeepLesion. Second, missing annotations in DeepLesion are retrieved by a new method of embedding matching that exploits clinical prior knowledge. Last, we discover suspicious but unannotated lesions using knowledge transfer from single-type lesion detectors. In this way, reliable positive and negative regions are obtained from partially-labeled and unlabeled images, which are effectively utilized to train ULD. To assess the clinically realistic protocol of 3D volumetric ULD, we fully annotated 1071 CT sub-volumes in DeepLesion. Our method outperforms the current state-of-the-art approach by 29% in the metric of average sensitivity.

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