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Image-based consensus molecular subtyping in rectal cancer biopsies and response to neoadjuvant chemoradiotherapy.
Lafarge, Maxime W; Domingo, Enric; Sirinukunwattana, Korsuk; Wood, Ruby; Samuel, Leslie; Murray, Graeme; Richman, Susan D; Blake, Andrew; Sebag-Montefiore, David; Gollins, Simon; Klieser, Eckhard; Neureiter, Daniel; Huemer, Florian; Greil, Richard; Dunne, Philip; Quirke, Philip; Weiss, Lukas; Rittscher, Jens; Maughan, Tim; Koelzer, Viktor H.
Afiliação
  • Lafarge MW; Department of Pathology and Molecular Pathology, University Hospital Zurich, University of Zurich, Zurich, Switzerland.
  • Domingo E; Department of Oncology, Medical Sciences Division, University of Oxford, Oxford, UK.
  • Sirinukunwattana K; Ground Truth Labs, Oxford, UK.
  • Wood R; Department of Engineering Science, Institute of Biomedical Engineering (IBME), University of Oxford, Oxford, UK.
  • Samuel L; Department of Engineering Science, University of Oxford, Oxford, UK.
  • Murray G; School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, UK.
  • Richman SD; School of Medicine, Medical Sciences and Nutrition, University of Aberdeen, Aberdeen, UK.
  • Blake A; Leeds Institute of Medical Research, University of Leeds, Leeds, UK.
  • Sebag-Montefiore D; Department of Oncology, Medical Sciences Division, University of Oxford, Oxford, UK.
  • Gollins S; Leeds Institute of Medical Research, University of Leeds, Leeds, UK.
  • Klieser E; North Wales Cancer Treatment Centre, Besti Cadwaladr University Health Board, Bodelwyddan, UK.
  • Neureiter D; Institute of Pathology, Paracelsus Medical University, Salzburg, Austria.
  • Huemer F; Institute of Pathology, Paracelsus Medical University, Salzburg, Austria.
  • Greil R; Department of Internal Medicine III with Haematology, Medical Oncology, Haemostaseology, Infectiology and Rheumatology, Oncologic Center, Salzburg Cancer Research Institute-Laboratory for Immunological and Molecular Cancer Research (SCRI-LIMCR), Paracelsus Medical University Salzburg, Salzburg, Aust
  • Dunne P; Department of Internal Medicine III with Haematology, Medical Oncology, Haemostaseology, Infectiology and Rheumatology, Oncologic Center, Salzburg Cancer Research Institute-Laboratory for Immunological and Molecular Cancer Research (SCRI-LIMCR), Paracelsus Medical University Salzburg, Salzburg, Aust
  • Quirke P; The Patrick G Johnston Centre for Cancer Research, Queens University Belfast, Belfast, UK.
  • Weiss L; Leeds Institute of Medical Research, University of Leeds, Leeds, UK.
  • Rittscher J; Department of Internal Medicine III with Haematology, Medical Oncology, Haemostaseology, Infectiology and Rheumatology, Oncologic Center, Salzburg Cancer Research Institute-Laboratory for Immunological and Molecular Cancer Research (SCRI-LIMCR), Paracelsus Medical University Salzburg, Salzburg, Aust
  • Maughan T; Department of Engineering Science, Institute of Biomedical Engineering (IBME), University of Oxford, Oxford, UK.
  • Koelzer VH; NIHR Oxford Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
NPJ Precis Oncol ; 8(1): 89, 2024 Apr 09.
Article em En | MEDLINE | ID: mdl-38594327
ABSTRACT
The development of deep learning (DL) models to predict the consensus molecular subtypes (CMS) from histopathology images (imCMS) is a promising and cost-effective strategy to support patient stratification. Here, we investigate whether imCMS calls generated from whole slide histopathology images (WSIs) of rectal cancer (RC) pre-treatment biopsies are associated with pathological complete response (pCR) to neoadjuvant long course chemoradiotherapy (LCRT) with single agent fluoropyrimidine. DL models were trained to classify WSIs of colorectal cancers stained with hematoxylin and eosin into one of the four CMS classes using a multi-centric dataset of resection and biopsy specimens (n = 1057 WSIs) with paired transcriptional data. Classifiers were tested on a held out RC biopsy cohort (ARISTOTLE) and correlated with pCR to LCRT in an independent dataset merging two RC cohorts (ARISTOTLE, n = 114 and SALZBURG, n = 55 patients). DL models predicted CMS with high classification performance in multiple comparative analyses. In the independent cohorts (ARISTOTLE, SALZBURG), cases with WSIs classified as imCMS1 had a significantly higher likelihood of achieving pCR (OR = 2.69, 95% CI 1.01-7.17, p = 0.048). Conversely, imCMS4 was associated with lack of pCR (OR = 0.25, 95% CI 0.07-0.88, p = 0.031). Classification maps demonstrated pathologist-interpretable associations with high stromal content in imCMS4 cases, associated with poor outcome. No significant association was found in imCMS2 or imCMS3. imCMS classification of pre-treatment biopsies is a fast and inexpensive solution to identify patient groups that could benefit from neoadjuvant LCRT. The significant associations between imCMS1/imCMS4 with pCR suggest the existence of predictive morphological features that could enhance standard pathological assessment.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article