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Image-based consensus molecular subtype (imCMS) classification of colorectal cancer using deep learning.
Sirinukunwattana, Korsuk; Domingo, Enric; Richman, Susan D; Redmond, Keara L; Blake, Andrew; Verrill, Clare; Leedham, Simon J; Chatzipli, Aikaterini; Hardy, Claire; Whalley, Celina M; Wu, Chieh-Hsi; Beggs, Andrew D; McDermott, Ultan; Dunne, Philip D; Meade, Angela; Walker, Steven M; Murray, Graeme I; Samuel, Leslie; Seymour, Matthew; Tomlinson, Ian; Quirke, Phil; Maughan, Timothy; Rittscher, Jens; Koelzer, Viktor H.
Afiliación
  • Sirinukunwattana K; Institute of Biomedical Engineering (IBME), Department of Engineering Science, University of Oxford, Oxford, UK.
  • Domingo E; Big Data Institute, University of Oxford, Li Ka Shing Centre for Health Information and Discovery, Oxford, UK.
  • Richman SD; Oxford NIHR Biomedical Research Centre, Oxford University Hospitals Trust, Oxford, UK.
  • Redmond KL; Department of Oncology, University of Oxford, Oxford, UK viktor.koelzer@usz.ch jens.rittscher@eng.ox.ac.uk enric.domingo@oncology.ox.ac.uk.
  • Blake A; Department of Pathology and Tumour Biology, Leeds Institute of Cancer and Pathology, Leeds, UK.
  • Verrill C; Centre for Cancer Research and Cell Biology, Faculty of Medicine, Health and Life Sciences, Queen's University Belfast, Belfast, UK.
  • Leedham SJ; Department of Oncology, University of Oxford, Oxford, UK.
  • Chatzipli A; Oxford NIHR Biomedical Research Centre, Oxford University Hospitals Trust, Oxford, UK.
  • Hardy C; Department of Cellular Pathology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Whalley CM; Nuffield Department of Surgical Sciences and NIHR Oxford Biomedical Research Centre, University of Oxford, Oxford, UK.
  • Wu CH; Gastrointestinal Stem-cell Biology Laboratory, Oxford Centre for Cancer Gene Research, Wellcome Trust Centre for Human Genetics, Oxford, UK.
  • Beggs AD; Translational Gastroenterology Unit, Experimental Medicine Division, Nuffield Department of Clinical Medicine, John Radcliffe Hospital, University of Oxford, Oxford, UK.
  • McDermott U; Wellcome Trust Sanger Institute, Hinxton, UK.
  • Dunne PD; Wellcome Trust Sanger Institute, Hinxton, UK.
  • Meade A; Institute of Cancer and Genomic Sciences, University of Birmingham, Birmingham, UK.
  • Walker SM; Department of Statistics, University of Oxford, Oxford, UK.
  • Murray GI; School of Cancer Sciences, University of Birmingham, Birmingham, UK.
  • Samuel L; Wellcome Trust Sanger Institute, Hinxton, UK.
  • Seymour M; Centre for Cancer Research and Cell Biology, Queen's University Belfast, Belfast, UK.
  • Tomlinson I; MRC Clinical Trials Unit at University College London, London, UK.
  • Quirke P; Almac Diagnostics Ltd, Craigavon, UK.
  • Maughan T; Department of Pathology, School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, UK.
  • Rittscher J; Department of Clinical Oncology, Aberdeen Royal Infirmary, Aberdeen, UK.
  • Koelzer VH; Department of Oncology, Leeds Institute of Cancer and Pathology, Leeds, UK.
Gut ; 70(3): 544-554, 2021 03.
Article en En | MEDLINE | ID: mdl-32690604
ABSTRACT

OBJECTIVE:

Complex phenotypes captured on histological slides represent the biological processes at play in individual cancers, but the link to underlying molecular classification has not been clarified or systematised. In colorectal cancer (CRC), histological grading is a poor predictor of disease progression, and consensus molecular subtypes (CMSs) cannot be distinguished without gene expression profiling. We hypothesise that image analysis is a cost-effective tool to associate complex features of tissue organisation with molecular and outcome data and to resolve unclassifiable or heterogeneous cases. In this study, we present an image-based approach to predict CRC CMS from standard H&E sections using deep learning.

DESIGN:

Training and evaluation of a neural network were performed using a total of n=1206 tissue sections with comprehensive multi-omic data from three independent datasets (training on FOCUS trial, n=278 patients; test on rectal cancer biopsies, GRAMPIAN cohort, n=144 patients; and The Cancer Genome Atlas (TCGA), n=430 patients). Ground truth CMS calls were ascertained by matching random forest and single sample predictions from CMS classifier.

RESULTS:

Image-based CMS (imCMS) accurately classified slides in unseen datasets from TCGA (n=431 slides, AUC)=0.84) and rectal cancer biopsies (n=265 slides, AUC=0.85). imCMS spatially resolved intratumoural heterogeneity and provided secondary calls correlating with bioinformatic prediction from molecular data. imCMS classified samples previously unclassifiable by RNA expression profiling, reproduced the expected correlations with genomic and epigenetic alterations and showed similar prognostic associations as transcriptomic CMS.

CONCLUSION:

This study shows that a prediction of RNA expression classifiers can be made from H&E images, opening the door to simple, cheap and reliable biological stratification within routine workflows.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: ARN / Neoplasias Colorrectales / Regulación Neoplásica de la Expresión Génica / Aprendizaje Profundo Tipo de estudio: Guideline / Prognostic_studies Límite: Humans Idioma: En Revista: Gut Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: ARN / Neoplasias Colorrectales / Regulación Neoplásica de la Expresión Génica / Aprendizaje Profundo Tipo de estudio: Guideline / Prognostic_studies Límite: Humans Idioma: En Revista: Gut Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido