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2019 | OriginalPaper | Buchkapitel

Improving Pathological Structure Segmentation via Transfer Learning Across Diseases

verfasst von : Barleen Kaur, Paul Lemaître, Raghav Mehta, Nazanin Mohammadi Sepahvand, Doina Precup, Douglas Arnold, Tal Arbel

Erschienen in: Domain Adaptation and Representation Transfer and Medical Image Learning with Less Labels and Imperfect Data

Verlag: Springer International Publishing

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Abstract

One of the biggest challenges in developing robust machine learning techniques for medical image analysis is the lack of access to large-scale annotated image datasets needed for supervised learning. When the task is to segment pathological structures (e.g. lesions, tumors) from patient images, training on a dataset with few samples is very challenging due to the large class imbalance and inter-subject variability. In this paper, we explore how to best leverage a segmentation model that has been pre-trained on a large dataset of patients images with one disease in order to successfully train a deep learning pathology segmentation model for a different disease, for which only a relatively small patient dataset is available. Specifically, we train a UNet model on a large-scale, proprietary, multi-center, multi-scanner Multiple Sclerosis (MS) clinical trial dataset containing over 3500 multi-modal MRI samples with expert-derived lesion labels. We explore several transfer learning approaches to leverage the learned MS model for the task of multi-class brain tumor segmentation on the BraTS 2018 dataset. Our results indicate that adapting and fine-tuning the encoder and decoder of the network trained on the larger MS dataset leads to improvement in brain tumor segmentation when few instances are available. This type of transfer learning outperforms training and testing the network on the BraTS dataset from scratch as well as several other transfer learning approaches, particularly when only a small subset of the dataset is available.

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Fußnoten
1
Please note that the predictions made on the BraTS 2018 Validation set must contain all four tumor sub-classes, which are then uploaded onto the BraTS web portal for evaluation.
 
4
The percentage improvement is calculated as the ratio of difference in the baseline and FT-All Dice scores over the baseline.
 
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Metadaten
Titel
Improving Pathological Structure Segmentation via Transfer Learning Across Diseases
verfasst von
Barleen Kaur
Paul Lemaître
Raghav Mehta
Nazanin Mohammadi Sepahvand
Doina Precup
Douglas Arnold
Tal Arbel
Copyright-Jahr
2019
DOI
https://doi.org/10.1007/978-3-030-33391-1_11