A Deep Learning Framework with Explainability for the Prediction of Lateral Locoregional Recurrences in Rectal Cancer Patients with Suspicious Lateral Lymph Nodes

Author:

Sluckin Tania C.123,Hekhuis Marije1,Kol Sabrine Q.4ORCID,Nederend Joost5ORCID,Horsthuis Karin34,Beets-Tan Regina G. H.678,Beets Geerard L.69ORCID,Burger Jacobus W. A.10,Tuynman Jurriaan B.123ORCID,Rutten Harm J. T.10,Kusters Miranda123,Benson Sean711ORCID

Affiliation:

1. Department of Surgery, Amsterdam UMC Location Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands

2. Cancer Center Amsterdam, Treatment and Quality of Life, 1081 HV Amsterdam, The Netherlands

3. Cancer Center Amsterdam, Imaging and Biomarkers, 1081 HV Amsterdam, The Netherlands

4. Department of Radiology, Amsterdam UMC Location Vrije Universiteit Amsterdam, 1081 HV Amsterdam, The Netherlands

5. Department of Radiology, Catharina Hospital, 5623 EJ Eindhoven, The Netherlands

6. GROW School for Oncology & Developmental Biology, Maastricht University, 6211 LK Maastricht, The Netherlands

7. Department of Radiology, Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands

8. Department of Clinical Radiology, University of Southern Denmark, Odense University Hospital, 5000 Odense, Denmark

9. Department of Surgery, Netherlands Cancer Institute, 1066 CX Amsterdam, The Netherlands

10. Department of Surgery, Catharina Hospital, 5623 EJ Eindhoven, The Netherlands

11. Department of Cardiology, Amsterdam University Medical Centers, University of Amsterdam, 1075 AX Amsterdam, The Netherlands

Abstract

Malignant lateral lymph nodes (LLNs) in low, locally advanced rectal cancer can cause (ipsi-lateral) local recurrences ((L)LR). Accurate identification is, therefore, essential. This study explored LLN features to create an artificial intelligence prediction model, estimating the risk of (L)LR. This retrospective multicentre cohort study examined 196 patients diagnosed with rectal cancer between 2008 and 2020 from three tertiary centres in the Netherlands. Primary and restaging T2W magnetic resonance imaging and clinical features were used. Visible LLNs were segmented and used for a multi-channel convolutional neural network. A deep learning model was developed and trained for the prediction of (L)LR according to malignant LLNs. Combined imaging and clinical features resulted in AUCs of 0.78 and 0.80 for LR and LLR, respectively. The sensitivity and specificity were 85.7% and 67.6%, respectively. Class activation map explainability methods were applied and consistently identified the same high-risk regions with structural similarity indices ranging from 0.772–0.930. This model resulted in good predictive value for (L)LR rates and can form the basis of future auto-segmentation programs to assist in the identification of high-risk patients and the development of risk stratification models.

Publisher

MDPI AG

Subject

Clinical Biochemistry

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