Deep learning-based segmentation of multisite disease in ovarian cancer.
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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. 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" framework and unrevised trainee radiologist segmentations. A total of 451 CT scans collected from four different institutions were used for training (n = 276), evaluation (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. RESULTS: Our model outperformed no-new-Net for the pelvic/ovarian lesions in cross-validation, on the evaluation and test set by a significant margin (p values being 4 × 10-7, 3 × 10-4, 4 × 10-2, respectively), and for the omental lesions on the evaluation set (p = 1 × 10-3). Our model did not perform significantly differently in segmenting pelvic/ovarian lesions (p = 0.371) compared to a trainee radiologist. On an independent test set, the model achieved a DSC performance of 71 ± 20 (mean ± standard deviation) for pelvic/ovarian and 61 ± 24 for omental lesions. CONCLUSION: Automated ovarian cancer segmentation on CT scans using deep neural networks is feasible and achieves performance close to a trainee-level radiologist for pelvic/ovarian lesions. RELEVANCE STATEMENT: Automated segmentation of ovarian cancer may be used by clinicians for CT-based volumetric assessments and researchers for building complex analysis pipelines. KEY POINTS: • The first automated approach for pelvic/ovarian and omental ovarian cancer lesion segmentation on CT images has been presented. • Automated segmentation of ovarian cancer lesions can be comparable with manual segmentation of trainee radiologists. • Careful hyperparameter tuning can provide models significantly outperforming strong state-of-the-art baselines.
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Acknowledgements: The authors would like to thank Fabian Isensee for making the nnU-Net library both freely available and easy to use for new datasets. This work was partially supported by The Mark Foundation for Cancer Research and Cancer Research UK Cambridge Centre [C9685/A25177], the Wellcome Trust Innovator Award [RG98755], the EPSRC IAA grant [EP/R511675/1] and the CRUK National Cancer Imaging Translational Accelerator (NCITA) [C42780/A27066]. Additional support was also provided by the National Institute of Health Research (NIHR) Cambridge Biomedical Research Centre (BRC-1215-20014). The views expressed are those of the authors and not necessarily those of the NHS, the NIHR or the Department of Health and Social Care. This project has been funded in whole or in part with Federal funds from the National Cancer Institute, National Institutes of Health, Department of Health and Human Services, under Contract No. 75N91019D00024. CBS acknowledges support from the Leverhulme Trust project on ‘Breaking the non-convexity barrier’; the Philip Leverhulme Prize; the Royal Society Wolfson Fellowship; the EPSRC grants EP/S026045/1 and EP/T003553/1, EP/N014588/1, EP/T017961/1, European Union Horizon 2020 research and innovation programmes under the Marie Skodowska-Curie grant agreement No. 777826 NoMADS and No. 691070 CHiPS; the Cantab Capital Institute for the Mathematics of Information; and the Alan Turing Institute. The work by Öktem was supported by the Swedish Foundation of Strategic Research under Grants AM13-0049. Microsoft Radiomics was provided to Addenbrooke’s Hospital (Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK) by the Microsoft InnerEye project.
Funder: Leverhulme Trust; doi: http://dx.doi.org/10.13039/501100000275
Funder: Philip Leverhulme Prize
Funder: Royal Society Wolfson
Funder: Cantab Capital Institute for the Mathematics of Infrormation
Funder: Stiftelsen för Strategisk Forskning; doi: http://dx.doi.org/10.13039/501100001729
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2509-9280
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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)
Cancer Research UK (22905)
Cancer Research UK (15601)

