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Serum carcinoembryonic antigen trends for diagnosing colorectal cancer recurrence in the FACS randomized clinical trial.
Shinkins, B; Primrose, J N; Pugh, S A; Nicholson, B D; Perera, R; James, T; Mant, D.
Afiliação
  • Shinkins B; Test Evaluation Group, Academic Unit of Health Economics, University of Leeds, Leeds, UK.
  • Primrose JN; University Surgery, University of Southampton, Southampton, UK.
  • Pugh SA; University Surgery, University of Southampton, Southampton, UK.
  • Nicholson BD; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Perera R; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • James T; Department of Clinical Biochemistry, John Radcliffe Hospital, Oxford University Hospitals NHS Foundation Trust, Oxford, UK.
  • Mant D; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
Br J Surg ; 105(6): 658-662, 2018 05.
Article em En | MEDLINE | ID: mdl-29579327
BACKGROUND: Most guidelines recommend that patients who have undergone curative resection for primary colorectal cancer are followed up for 5 years with regular blood carcinoembryonic antigen (CEA) tests to trigger further investigation for recurrence. However, CEA may miss recurrences, or patients may have false alarms and undergo unnecessary investigation. METHODS: The diagnostic accuracy of trends in CEA measurements for recurrent colorectal cancer, taken as part of the FACS (Follow-up After Colorectal Surgery) trial (2003-2014), were analysed. Investigation to detect recurrence was triggered by clinical symptoms, scheduled CT or colonoscopy, or a CEA level of at least 7 µg/l above baseline. Time-dependent receiver operating characteristic (ROC) curve analysis was used to compare the diagnostic accuracy of CEA trends with single measurements. CEA trends were estimated using linear regression. RESULTS: The area under the ROC curve (AUC) for CEA trend was at least 0·820 across all 5 years of follow-up. In comparison, the AUCs for single measurements ranged from 0·623 to 0·749. Improvement was most marked at the end of the first year of follow-up, with the AUC increasing from 0·623 (95 per cent c.i. 0·509 to 0·736) to 0·880 (0·814 to 0·947). However, no individual trend threshold achieved a sensitivity above 70 per cent (30 per cent missed recurrences). CONCLUSION: Interpreting trends in CEA measurements instead of single CEA test results improves diagnostic accuracy for recurrence, but not sufficiently to warrant it being used as a single surveillance strategy to trigger further investigation. In the absence of a more accurate biomarker, monitoring trends in CEA should be combined with clinical, endoscopic and imaging surveillance for improved accuracy.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Antígeno Carcinoembrionário / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Limite: Aged / Aged80 / Humans / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Antígeno Carcinoembrionário / Recidiva Local de Neoplasia Tipo de estudo: Clinical_trials / Diagnostic_studies / Guideline / Prognostic_studies Limite: Aged / Aged80 / Humans / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article