Clinical validity of detecting K-ras mutations for the diagnosis of exocrine pancreatic cancer: a prospective study in a clinically-relevant spectrum of patients
Autor: | Francisco X. Real, Miquel Porta, Joan Alguacil, Núria Malats, Ildefonso Hernández-Aguado, Blanca Lumbreras, Lucy Anne Parker, Esteve Fernández, Juli Rifà, Luisa Guarner, Alfredo Carrato, Tomàs López, Josep M. Corominas |
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Přispěvatelé: | Department of Public Health, Miguel Hernández University, CIBER en Epidemiología y Salud Pública (CIBERESP), CIBER de Epidemiología y Salud Pública (CIBERESP), Facultat de Medicina, Universitat Autònoma de Barcelona (UAB), IMIM-Hospital del Mar, Generalitat de Catalunya, Vall d'Hebron University Hospital [Barcelona], Hospital Universitario Ramón y Cajal [Madrid], Universidad de Alcalá - University of Alcalá (UAH), Hospital Son Dureta, Catalan Institute of Oncology (ICO), Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), University of Barcelona, Universidad de Huelva, Centro Nacional de Investigaciones Oncológicas, Universitat Pompeu Fabra [Barcelona] (UPF) |
Rok vydání: | 2011 |
Předmět: |
Male
medicine.medical_specialty Pathology Pancreatic disease Epidemiology Diagnosis/analysis Polymerase Chain Reaction Sensitivity and Specificity Gastroenterology Epidemiology/diagnosis 03 medical and health sciences 0302 clinical medicine Internal medicine Diagnosis/diagnostic use medicine Humans Oncogene protein p21 ras Prospective Studies 030212 general & internal medicine Medical diagnosis Prospective cohort study KRAS oncogene ras Aged Aged 80 and over business.industry Reproducibility of Results Cancer Middle Aged medicine.disease Omics Pancreatic neoplasms/diagnosis 3. Good health Pancreatic Neoplasms Diagnosis/methods Genes ras Genes 030220 oncology & carcinogenesis Mutation Pancreatitis Exocrine pancreatic cancer [SDV.SPEE]Life Sciences [q-bio]/Santé publique et épidémiologie Female Pancreatic cysts business Research/methods Polymorphism Restriction Fragment Length |
Zdroj: | European Journal of Epidemiology European Journal of Epidemiology, Springer Verlag, 2011, 26 (3), pp.229-236. ⟨10.1007/s10654-011-9547-8⟩ |
ISSN: | 1573-7284 0393-2990 |
DOI: | 10.1007/s10654-011-9547-8 |
Popis: | International audience; The diagnostic utility of detecting K- mutations for the diagnosis of exocrine pancreatic cancer (EPC) has not been properly studied, and few reports have analysed a clinically relevant spectrum of patients. The objective was to evaluate the clinical validity of detecting K- mutations in the diagnosis of EPC in a large sample of clinically relevant patients. We prospectively identified 374 patients in whom one of the following diagnoses was suspected at hospital admission: EPC, chronic pancreatitis, pancreatic cysts, and cancer of the extrahepatic biliary system. Mutations in the K- oncogene were analysed by PCR and artificial RFLP in 212 patients. The sensitivity and specificity of the K- mutational status for the diagnosis of EPC were 77.7% (95% CI: 69.2-84.8) and 78.0% (68.1-86.0), respectively. The diagnostic accuracy was hardly modified by sex and age. In patients with either mutated K- or CEA > 5 ng/ml, the sensitivity and specificity were 81.0% (72.9-87.6) and 62.6% (72.9-87.6), respectively. In patients with mutated K- and CEA > 5 ng/ml the sensitivity was markedly reduced. In comparisons with a variety of non-EPC patient groups sensitivity and specificity were both always greater than 75%. In this clinically relevant sample of patients the sensitivity and specificity of K- mutations were not sufficiently high for independent diagnostic use. However, it seems premature to rule out the utility of K- analysis in conjunction with other genetic and 'omics' technologies. |
Databáze: | OpenAIRE |
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