Universal Lesion Detection by Learning from Multiple Heterogeneously
Labeled Datasets
- URL: http://arxiv.org/abs/2005.13753v1
- Date: Thu, 28 May 2020 02:56:00 GMT
- Title: Universal Lesion Detection by Learning from Multiple Heterogeneously
Labeled Datasets
- Authors: Ke Yan, Jinzheng Cai, Adam P. Harrison, Dakai Jin, Jing Xiao, Le Lu
- Abstract summary: We learn a multi-head multi-task lesion detector using all datasets and generate lesion proposals on DeepLesion.
We discover suspicious but unannotated lesions using knowledge transfer from single-type lesion detectors.
Our method outperforms the current state-of-the-art approach by 29% in the metric of average sensitivity.
- Score: 23.471903581482668
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: 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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