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The diagnostic accuracy of a single CEA blood test in detecting colorectal cancer recurrence: Results from the FACS trial.
Shinkins, Bethany; Nicholson, Brian D; Primrose, John; Perera, Rafael; James, Timothy; Pugh, Sian; Mant, David.
Afiliação
  • Shinkins B; Test Evaluation Group, Academic Unit of Health Economics, University of Leeds, Leeds, United Kingdom.
  • Nicholson BD; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, United Kingdom.
  • Primrose J; Academic Unit of Cancer Sciences, University of Southampton, Southampton, United Kingdom.
  • Perera R; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, United Kingdom.
  • James T; Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom.
  • Pugh S; Academic Unit of Cancer Sciences, University of Southampton, Southampton, United Kingdom.
  • Mant D; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, United Kingdom.
PLoS One ; 12(3): e0171810, 2017.
Article em En | MEDLINE | ID: mdl-28282381
OBJECTIVE: To evaluate the diagnostic accuracy of a single CEA (carcinoembryonic antigen) blood test in detecting colorectal cancer recurrence. BACKGROUND: Patients who have undergone curative resection for primary colorectal cancer are typically followed up with scheduled CEA testing for 5 years. Decisions to investigate further (usually by CT imaging) are based on single test results, reflecting international guidelines. METHODS: A secondary analysis was undertaken of data from the FACS trial (two arms included CEA testing). The composite reference standard applied included CT-CAP imaging, clinical assessment and colonoscopy. Accuracy in detecting recurrence was evaluated in terms of sensitivity, specificity, likelihood ratios, predictive values, time-dependent area under the ROC curves, and operational performance when used prospectively in clinical practice are reported. RESULTS: Of 582 patients, 104 (17.9%) developed recurrence during the 5 year follow-up period. Applying the recommended threshold of 5µg/L achieves at best 50.0% sensitivity (95% CI: 40.1-59.9%); in prospective use in clinical practice it would lead to 56 missed recurrences (53.8%; 95% CI: 44.2-64.4%) and 89 false alarms (56.7% of 157 patients referred for investigation). Applying a lower threshold of 2.5µg/L would reduce the number of missed recurrences to 36.5% (95% CI: 26.5-46.5%) but would increase the false alarms to 84.2% (924/1097 referred). Some patients are more prone to false alarms than others-at the 5µg/L threshold, the 89 episodes of unnecessary investigation were clustered in 29 individuals. CONCLUSION: Our results demonstrated very low sensitivity for CEA, bringing to question whether it could ever be used as an independent triage test. It is not feasible to improve the diagnostic performance of a single test result by reducing the recommended action threshold because of the workload and false alarms generated. Current national and international guidelines merit re-evaluation and options to improve performance, such as making clinical decisions on the basis of CEA trend, should be further assessed.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Antígeno Carcinoembrionário / Recidiva Local de Neoplasia Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Antígeno Carcinoembrionário / Recidiva Local de Neoplasia Idioma: En Ano de publicação: 2017 Tipo de documento: Article