Deep learning identifies inflamed fat as a risk factor for lymph node metastasis in early colorectal cancer

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Scarlet Brockmoeller - , University of Leeds (Author)
  • Amelie Echle - , University Hospital Aachen (Author)
  • Narmin Ghaffari Laleh - , University Hospital Aachen (Author)
  • Susanne Eiholm - , University of Copenhagen (Author)
  • Marie Louise Malmstrøm - , Nordsjællands Hospital (Author)
  • Tine Plato Kuhlmann - , Copenhagen University Hospitals (Author)
  • Katarina Levic - , Copenhagen University Hospitals (Author)
  • Heike Irmgard Grabsch - , University of Leeds (Author)
  • Nicholas P West - , University of Leeds (Author)
  • Oliver Lester Saldanha - , University Hospital Aachen (Author)
  • Katerina Kouvidi - , University of Leeds (Author)
  • Aurora Bono - , University of Leeds (Author)
  • Lara R Heij - , Maastricht University (Author)
  • Titus J Brinker - , German Cancer Research Center (DKFZ) (Author)
  • Ismayil Gögenür - , University of Copenhagen (Author)
  • Philip Quirke - , University of Leeds (Author)
  • Jakob Nikolas Kather - , Leeds Teaching Hospitals NHS Trust, University of Leeds, University Hospital Aachen, National Center for Tumor Diseases (NCT) Heidelberg (Author)

Abstract

The spread of early-stage (T1 and T2) adenocarcinomas to locoregional lymph nodes is a key event in disease progression of colorectal cancer (CRC). The cellular mechanisms behind this event are not completely understood and existing predictive biomarkers are imperfect. Here, we used an end-to-end deep learning algorithm to identify risk factors for lymph node metastasis (LNM) status in digitized histopathology slides of the primary CRC and its surrounding tissue. In two large population-based cohorts, we show that this system can predict the presence of more than one LNM in pT2 CRC patients with an area under the receiver operating curve (AUROC) of 0.733 (0.67-0.758) and patients with any LNM with an AUROC of 0.711 (0.597-0.797). Similarly, in pT1 CRC patients, the presence of more than one LNM or any LNM was predictable with an AUROC of 0.733 (0.644-0.778) and 0.567 (0.542-0.597), respectively. Based on these findings, we used the deep learning system to guide human pathology experts towards highly predictive regions for LNM in the whole slide images. This hybrid human observer and deep learning approach identified inflamed adipose tissue as the highest predictive feature for LNM presence. Our study is a first proof of concept that artificial intelligence (AI) systems may be able to discover potentially new biological mechanisms in cancer progression. Our deep learning algorithm is publicly available and can be used for biomarker discovery in any disease setting. © 2021 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Details

Original languageEnglish
Pages (from-to)269-281
Number of pages13
JournalThe Journal of pathology
Volume256
Issue number3
Publication statusPublished - Mar 2022
Peer-reviewedYes
Externally publishedYes

External IDs

Scopus 85121997885

Keywords

Sustainable Development Goals

Keywords

  • Adipose Tissue/pathology, Biopsy, Colorectal Neoplasms/pathology, Deep Learning, Diagnosis, Computer-Assisted, Early Detection of Cancer, Humans, Image Interpretation, Computer-Assisted, Lymph Nodes/pathology, Lymphatic Metastasis, Microscopy, Neoplasm Staging, Predictive Value of Tests, Proof of Concept Study, Reproducibility of Results, Retrospective Studies, Risk Assessment, Risk Factors

Library keywords