4.7 Article

Comparison and combination of blood-based inflammatory markers with faecal occult blood tests for non-invasive colorectal cancer screening

Journal

BRITISH JOURNAL OF CANCER
Volume 106, Issue 8, Pages 1424-1430

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/bjc.2012.104

Keywords

inflammatory markers; faecal occult blood tests; colorectal cancer screening

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Funding

  1. German Research Foundation [Graduiertenkolleg 793]
  2. German Cancer Research Centre

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BACKGROUND: Faecal occult blood tests (FOBTs) are widely used for colorectal cancer (CRC) screening. Blood-based inflammatory markers have been suggested as alternative or supplementary non-invasive CRC screening tests. METHODS: Among 179 CRC patients, 193 people with advanced adenoma and 225 people free of neoplasm, C-reactive protein (CRP), serum CD26 (sCD26), complement C3a anaphylatoxin and tissue inhibitor of metalloproteinases 1 (TIMP-1) levels in blood were measured by ELISA tests, and an immunochemical FOBT (iFOBT) and a guaiac-based FOBT were performed. Receiver operating characteristic curves were constructed and the areas under the curves (AUCs) were compared. RESULTS: The blood levels of CRP, sCD26 and TIMP-1 showed statistically significant differences between CRC patients and neoplasm-free participants, and levels of TIMP-1 were furthermore significantly elevated in advanced adenoma patients. For the four inflammatory markers, AUCs ranged from 0.52 to 0.62 for CRC detection and from 0.50 to 0.58 for advanced adenomas detection, compared with AUCs of 0.90 and 0.68 for the iFOBT. At 97% specificity, blood markers showed much lower sensitivities than FOBTs. Combining inflammatory markers with the iFOBT increased the AUC for advanced adenomas. CONCLUSION: These blood-based markers do not seem to be an alternative to FOBT-based CRC screening. The potential use of these and other blood-based tests in combination with iFOBT might deserve further attention. British Journal of Cancer (2012) 106, 1424-1430. doi: 10.1038/bjc.2012.104 www.bjcancer.com Published online 27 March 2012 (C) 2012 Cancer Research UK

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