2017
DOI: 10.1177/2050640617737004
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Fecal immunochemical tests in combination with blood tests for colorectal cancer and advanced adenoma detection—systematic review

Abstract: Combining FIT and blood tests might be a promising approach to enhance sensitivity of CRC screening, but comprehensive evaluation of promising marker combinations in screening populations is needed.

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Cited by 17 publications
(14 citation statements)
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“…FIT has already been recommended by NICE DG30 to triage patients with low-risk symptoms 2 for investigation, but at the time was not been recommended for high-risk symptoms, due to a lack of robust evidence within the UK setting and because f-Hb are known to vary by age, [11][12][13] sex, [11][12][13] deprivation, 13 14 cancer stage, 33 IDA 19 27 and between homogeneous ethnic populations. 15 We investigated these known covariates and found that there was no significant difference in FIT sensitivity for CRC across all groups including cancer stage and IDA at cut-offs of 2 and 10 µg/g.…”
Section: Gi Cancermentioning
confidence: 99%
“…FIT has already been recommended by NICE DG30 to triage patients with low-risk symptoms 2 for investigation, but at the time was not been recommended for high-risk symptoms, due to a lack of robust evidence within the UK setting and because f-Hb are known to vary by age, [11][12][13] sex, [11][12][13] deprivation, 13 14 cancer stage, 33 IDA 19 27 and between homogeneous ethnic populations. 15 We investigated these known covariates and found that there was no significant difference in FIT sensitivity for CRC across all groups including cancer stage and IDA at cut-offs of 2 and 10 µg/g.…”
Section: Gi Cancermentioning
confidence: 99%
“…Thus, blood CRC biomarkers remain very attractive and are under investigation, including several molecules from nucleic acids such as DNA and various types of RNA (messenger, mRNA; micro, miRNA; long non-coding, lncRNA) to proteins, from circulating tumor cells to microvesicles. There is also growing interest in biomarker combination, which could obtain a higher sensitivity than single biomarker-based tests [ 72 , 75 , 76 ].…”
Section: New Testsmentioning
confidence: 99%
“…However, mSEPT9 is not able to distinguish between CRC and polyps or adenomas and seems not affected by tumor localization, but may be affected by age or sex, suggesting that age- and sex-specific cut-offs are required to better optimize the screening and diagnostic procedures [ 75 , 102 , 104 ]. The combination of mSEPT9 with the FIT test seems to improve the sensitivity for CRC and AA detection obtaining 94 and 43%, respectively, but at the cost of losing the specificity [ 76 ].…”
Section: New Testsmentioning
confidence: 99%
“…Focus on FIT screening results and emerging results from blood-based biomarker studies indicate that FIT screening has some location- and T stage-associated limitation in detecting neoplastic lesions [ 20 ], while blood-based biomarkers may have location-independent limitations with the T1 lesions of CRC and some adenomas [ 37 ]. Future achievements for improving CRC screening may therefore consider combinations of FIT and blood-based biomarkers [ 39 ]. Specifically, it may be considered that the combination identifies additional subjects with neoplastic lesions in comparison with the separate FIT or blood-based screening test, respectively.…”
mentioning
confidence: 99%