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Single-cell AI-based detection and prognostic and predictive value of DNA mismatch repair deficiency in colorectal cancer.
Nowak, Marta; Jabbar, Faiz; Rodewald, Ann-Katrin; Gneo, Luciana; Tomasevic, Tijana; Harkin, Andrea; Iveson, Tim; Saunders, Mark; Kerr, Rachel; Oein, Karin; Maka, Noori; Hay, Jennifer; Edwards, Joanne; Tomlinson, Ian; Sansom, Owen; Kelly, Caroline; Pezzella, Francesco; Kerr, David; Easton, Alistair; Domingo, Enric; Koelzer, Viktor H; Church, David N.
Afiliación
  • Nowak M; Department of Pathology and Molecular Pathology, Zurich, Zurich, Switzerland.
  • Jabbar F; Cancer Genomics and Immunology Group, The Wellcome Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.
  • Rodewald AK; Department of Pathology and Molecular Pathology, Zurich, Zurich, Switzerland.
  • Gneo L; Cancer Genomics and Immunology Group, The Wellcome Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.
  • Tomasevic T; Cancer Genomics and Immunology Group, The Wellcome Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK.
  • Harkin A; CRUK Glasgow Clinical Trials Unit, University of Glasgow, Glasgow, UK.
  • Iveson T; University of Southampton, Southampton, UK.
  • Saunders M; The Christie NHS Foundation Trust, Manchester, UK.
  • Kerr R; Department of Oncology, University of Oxford, Oxford, UK.
  • Oein K; Glasgow Tissue Research Facility, University of Glasgow, Queen Elizabeth University Hospital, Glasgow, UK.
  • Maka N; Glasgow Tissue Research Facility, University of Glasgow, Queen Elizabeth University Hospital, Glasgow, UK.
  • Hay J; Glasgow Tissue Research Facility, University of Glasgow, Queen Elizabeth University Hospital, Glasgow, UK.
  • Edwards J; School of Cancer Sciences, University of Glasgow, Glasgow, UK.
  • Tomlinson I; Department of Oncology, University of Oxford, Oxford, UK.
  • Sansom O; CRUK Beatson Institute of Cancer Research, Garscube Estate, Glasgow, UK.
  • Kelly C; CRUK Glasgow Clinical Trials Unit, University of Glasgow, Glasgow, UK.
  • Pezzella F; Radcliffe Department of Medicine, University of Oxford, Oxford, UK.
  • Kerr D; Nuffield Department of Clinical and Laboratory Sciences, University of Oxford, Oxford, UK.
  • Easton A; Department of Oncology, University of Oxford, Oxford, UK.
  • Domingo E; Department of Oncology, University of Oxford, Oxford, UK.
  • Koelzer VH; Department of Pathology and Molecular Pathology, Zurich, Zurich, Switzerland; Department of Oncology, University of Oxford, Oxford, UK; Nuffield Department of Medicine, University of Oxford, Oxford, UK; Institute of Medical Genetics and Pathology, University Hospital Basel, Basel, Switzerland.
  • Church DN; Cancer Genomics and Immunology Group, The Wellcome Centre for Human Genetics, University of Oxford, Roosevelt Drive, Oxford OX3 7BN, UK; Oxford NIHR Comprehensive Biomedical Research Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK. Electronic address: dchurch@well.ox.ac.uk.
Cell Rep Med ; 5(9): 101727, 2024 Sep 17.
Article en En | MEDLINE | ID: mdl-39293403
ABSTRACT
Testing for DNA mismatch repair deficiency (MMRd) is recommended for all colorectal cancers (CRCs). Automating this would enable precision medicine, particularly if providing information on etiology not captured by deep learning (DL) methods. We present AIMMeR, an AI-based method for determination of mismatch repair (MMR) protein expression at a single-cell level in routine pathology samples. AIMMeR shows an area under the receiver-operator curve (AUROC) of 0.98, and specificity of ≥75% at 98% sensitivity against pathologist ground truth in stage II/III in two trial cohorts, with positive predictive value of ≥98% for the commonest pattern of somatic MMRd. Lower agreement with microsatellite instability (MSI) testing (AUROC 0.86) reflects discordance between MMR and MSI PCR rather than AIMMeR misclassification. Analysis of the SCOT trial confirms MMRd prognostic value in oxaliplatin-treated patients; while MMRd does not predict differential benefit of chemotherapy duration, it correlates with difference in relapse by regimen (PInteraction = 0.04). AIMMeR may help reduce pathologist workload and streamline diagnostics in CRC.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Inestabilidad de Microsatélites / Reparación de la Incompatibilidad de ADN / Análisis de la Célula Individual Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cell Rep Med Año: 2024 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias Colorrectales / Inestabilidad de Microsatélites / Reparación de la Incompatibilidad de ADN / Análisis de la Célula Individual Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Cell Rep Med Año: 2024 Tipo del documento: Article País de afiliación: Suiza Pais de publicación: Estados Unidos