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A Cross-Sectional and Longitudinal Analysis of Pre-Diagnostic Blood Plasma Biomarkers for Early Detection of Pancreatic Cancer.
Mason, James; Lundberg, Erik; Jonsson, Pär; Nyström, Hanna; Franklin, Oskar; Lundin, Christina; Naredi, Peter; Antti, Henrik; Sund, Malin; Öhlund, Daniel.
Afiliação
  • Mason J; Department of Radiation Sciences, Umea University, 901 87 Umea, Sweden.
  • Lundberg E; Wallenberg Centre for Molecular Medicine, Umea University, 901 87 Umea, Sweden.
  • Jonsson P; Department of Surgical and Perioperative Sciences, Umea University, 901 87 Umea, Sweden.
  • Nyström H; Department of Chemistry, Umea University, 901 87 Umea, Sweden.
  • Franklin O; Wallenberg Centre for Molecular Medicine, Umea University, 901 87 Umea, Sweden.
  • Lundin C; Department of Surgical and Perioperative Sciences, Umea University, 901 87 Umea, Sweden.
  • Naredi P; Department of Surgical and Perioperative Sciences, Umea University, 901 87 Umea, Sweden.
  • Antti H; Department of Surgical and Perioperative Sciences, Umea University, 901 87 Umea, Sweden.
  • Sund M; Department of Surgery, Institute of Clinical Sciences, University of Gothenburg, 413 45 Gothenburg, Sweden.
  • Öhlund D; Department of Chemistry, Umea University, 901 87 Umea, Sweden.
Int J Mol Sci ; 23(21)2022 Oct 26.
Article em En | MEDLINE | ID: mdl-36361759
ABSTRACT
Pancreatic ductal adenocarcinoma (PDAC) is a major cause of cancer death that typically presents at an advanced stage. No reliable markers for early detection presently exist. The prominent tumor stroma represents a source of circulating biomarkers for use together with cancer cell-derived biomarkers for earlier PDAC diagnosis. CA19-9 and CEA (cancer cell-derived biomarkers), together with endostatin and collagen IV (stroma-derived) were examined alone, or together, by multivariable modelling, using pre-diagnostic plasma samples (n = 259 samples) from the Northern Sweden Health and Disease Study biobank. Serial samples were available for a subgroup of future patients. Marker efficacy for future PDAC case prediction (n = 154 future cases) was examined by both cross-sectional (ROC analysis) and longitudinal analyses. CA19-9 performed well at, and within, six months to diagnosis and multivariable modelling was not superior to CA19-9 alone in cross-sectional analysis. Within six months to diagnosis, CA19-9 (AUC = 0.92) outperformed the multivariable model (AUC = 0.81) at a cross-sectional level. At diagnosis, CA19-9 (AUC = 0.995) and the model (AUC = 0.977) performed similarly. Longitudinal analysis revealed increases in CA19-9 up to two years to diagnosis which indicates a window of opportunity for early detection of PDAC.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies / Observational_studies / Prevalence_studies / Prognostic_studies / Risk_factors_studies / Screening_studies Limite: Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article