Abstract

Simple SummaryThis study evaluates the impact of adding an object detection framework into brain tumour segmentation models, especially when the models are applied to different domains. In recent years, multiple models have been successfully applied to brain tumour segmentation tasks. However, the performance and stability of these models have never been evaluated when the training and target domain differ. In this study, we identify object detection as a simpler problem that can be injected into a segmentation model as an a priori, and which can increase the performance of our models. We propose an automatic segmentation model that, without model retraining or adaptation, showed good results when applied to a rare brain tumour.Tumour lesion segmentation is a key step to study and characterise cancer from MR neuroradiological images. Presently, numerous deep learning segmentation architectures have been shown to perform well on the specific tumour type they are trained on (e.g., glioblastoma in brain hemispheres). However, a high performing network heavily trained on a given tumour type may perform poorly on a rare tumour type for which no labelled cases allows training or transfer learning. Yet, because some visual similarities exist nevertheless between common and rare tumours, in the lesion and around it, one may split the problem into two steps: object detection and segmentation. For each step, trained networks on common lesions could be used on rare ones following a domain adaptation scheme without extra fine-tuning. This work proposes a resilient tumour lesion delineation strategy, based on the combination of established elementary networks that achieve detection and segmentation. Our strategy allowed us to achieve robust segmentation inference on a rare tumour located in an unseen tumour context region during training. As an example of a rare tumour, Diffuse Intrinsic Pontine Glioma (DIPG), we achieve an average dice score of 0.62 without further training or network architecture adaptation.

Highlights

  • Diffuse Intrinsic Pontine Glioma (DIPG) is a rare brain tumour located in the pons, mostly found in children between 5 and 7 years of age

  • This paper addresses the problem of rare tumour types, for which no database can be built to train a deep neural segmentation network

  • Our work shows that state-of-the-art segmentation methods perform poorly when applied on test cohorts on which they were not trained

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Summary

Introduction

Diffuse Intrinsic Pontine Glioma (DIPG) is a rare brain tumour located in the pons, mostly found in children between 5 and 7 years of age. It is considered one of the most aggressive paediatric tumours, with a survival rate of less than 10% beyond 2 years after diagnosis [1] and a median overall survival below 1 year [2]. The location of the tumour and its corresponding genomic alteration makes the DIPG a completely different type of tumour from other High Grade Glioma (HGG) [4]. Due to the tumour location and its infiltrating characteristics, alternatives are being actively sought to find non-invasive biomarkers to propose innovative therapies and improve treatment monitoring

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