Abstract

Accurate segmentation is an essential task when working with medical images. Recently, deep convolutional neural networks achieved a state-of-the-art performance for many segmentation benchmarks. Regardless of the network architecture, the deep learning-based segmentation methods view the segmentation problem as a supervised task that requires a relatively large number of annotated images. Acquiring a large number of annotated medical images is time consuming, and high-quality segmented images (i.e., strong labels) crafted by human experts are expensive. In this paper, we have proposed a method that achieves competitive accuracy from a “weakly annotated” image where the weak annotation is obtained via a 3D bounding box denoting an object of interest. Our method, called “3D-BoxSup,” employs a positive-unlabeled learning framework to learn segmentation masks from 3D bounding boxes. Specially, we consider the pixels outside of the bounding box as positively labeled data and the pixels inside the bounding box as unlabeled data. Our method can suppress the negative effects of pixels residing between the true segmentation mask and the 3D bounding box and produce accurate segmentation masks. We applied our method to segment a brain tumor. The experimental results on the BraTS 2017 dataset (Menze et al., 2015; Bakas et al., 2017a,b,c) have demonstrated the effectiveness of our method.

Highlights

  • Gliomas are one of the most common brain tumors in adults

  • We have proposed the “3D-BoxSup” method to train a deep convolutional neural network reliably from 3D bounding box annotations with a non-negative risk estimator that is robust against overfitting (Kiryo et al, 2017)

  • We conducted experiments on the BraTS 2017 dataset, and the results show that our method can obtain competitive accuracy by just learning from coarse bounding box annotations

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Summary

Introduction

Gliomas are one of the most common brain tumors in adults. They can be categorized into different levels of aggressiveness, including High-Grade Gliomas (HGG) and Lower Grade Gliomas (LGG) (Louis et al, 2016). Gliomas consist of heterogeneous histological sub-regions, including peritumoral edema, the necrotic core, as well as the enhancing and non-enhancing tumor core (Menze et al, 2015). Magnetic Resonance Imaging (MRI) of brain tumors is commonly used to evaluate tumor progression and plan treatments. An MRI usually contains multi-modal data, such as T1-weighted, T2-weighted, contrast enhanced T1-weighted (T1ce), and Fluid Attenuation Inversion Recovery (FLAIR) images, which provide complementary information for analysis of brain tumors.

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