Deep learning-based Segmentation of Multi-site Disease in Ovarian Cancer
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Abstract
Abstract
Purpose
To determine if pelvic/ovarian and omental lesions of ovarian cancer can be reliably segmented on computed tomography (CT) using fully automated deep learning-based methods.
Materials and Methods
A deep learning model for the two most common disease sites of high grade serous ovarian cancer lesions (pelvis/ovaries and omentum) was developed and compared against the well-established “no-new-Net” (nnU-Net) framework and unrevised trainee radiologist segmentations. A total of 451 pre-treatment and post neoadjuvant chemotherapy (NACT) CT scans collected from four different institutions were used for training (n=276), hyper-parameter tuning (n=104) and testing (n=71) of the methods. The performance was evaluated using the Dice similarity coefficient (DSC) and compared using a Wilcoxon test on paired results
Results
Our model outperforms the nnU-Net framework by a significant margin for both disease (validation: p=1×10-4,1.5×10-6, test: p=0.004, 0.005) and it does not perform significantly different from a trainee radiologist for the pelvic/ovarian lesions (p=0.392). On an independent test set (n=71), the model achieves a performance of 72±19 mean DSC for the pelvic/ovarian and 64±24 for the omental lesions.
Conclusion
Automated ovarian cancer segmentation on CT using deep neural networks is feasible and achieves performance close to a trainee-level radiologist for pelvic/ovarian lesions.
Summary
Deep learning-based models were used to assess whether fully automated segmentation is feasible for the main two disease sites in high grade serous ovarian cancer.
Key Points
First automated approach for pelvic/ovarian and omental ovarian cancer lesion segmentation on CT images.
Automated segmentation of ovarian cancer lesions can be comparable with manual segmentation of trainee radiologists with three years of experience in oncological and gynecological imaging.
Careful hyper-parameter tuning can provide models significantly outperforming strong state-of-the-art baselines.
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Keywords
32 Biomedical and Clinical Sciences, 3211 Oncology and Carcinogenesis, Biomedical Imaging, Networking and Information Technology R&D (NITRD), Clinical Research, Rare Diseases, Cancer, Bioengineering, Machine Learning and Artificial Intelligence, Minority Health, Women's Health, Ovarian Cancer, Cancer
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Except where otherwised noted, this item's license is described as All rights reserved
Sponsorship
Engineering and Physical Sciences Research Council (EP/N014588/1)
European Commission Horizon 2020 (H2020) Marie Sk?odowska-Curie actions (691070)
European Commission Horizon 2020 (H2020) Marie Sk?odowska-Curie actions (777826)
EPSRC (EP/S026045/1)
EPSRC (EP/T017961/1)
EPSRC (EP/T003553/1)
National Institute for Health and Care Research (IS-BRC-1215-20014)
Cancer Research UK (C96/A25177)
Royal Society
Wellcome Trust Ltd
European Commission
The Mark Foundation for Cancer Research
Cancer Research UK
Leverhulme Trust
Cambridge University Hospitals NHS Foundation Trust
National Institute for Health and Care Research
Microsoft Corp
Swedish Foundation for Strategic Research
UK Research and Innovation
National Institutes of Health
Engineering and Physical Sciences Research Council
European Commission Horizon 2020 (H2020) Marie Sk?odowska-Curie actions (691070)
European Commission Horizon 2020 (H2020) Marie Sk?odowska-Curie actions (777826)
EPSRC (EP/S026045/1)
EPSRC (EP/T017961/1)
EPSRC (EP/T003553/1)
National Institute for Health and Care Research (IS-BRC-1215-20014)
Cancer Research UK (C96/A25177)
Royal Society
Wellcome Trust Ltd
European Commission
The Mark Foundation for Cancer Research
Cancer Research UK
Leverhulme Trust
Cambridge University Hospitals NHS Foundation Trust
National Institute for Health and Care Research
Microsoft Corp
Swedish Foundation for Strategic Research
UK Research and Innovation
National Institutes of Health
Engineering and Physical Sciences Research Council
