Repeat Faecal Immunochemical Testing for Colorectal Cancer Detection in Symptomatic and Screening Patients: A Systematic Review and Meta-Analysis

被引:3
作者
Gerrard, Adam D. [1 ,2 ]
Garau, Roberta [1 ,2 ]
Xu, Wei [1 ,3 ]
Maeda, Yasuko [4 ,5 ]
Dunlop, Malcolm G. [1 ,6 ]
Theodoratou, Evropi [1 ,3 ]
Din, Farhat V. N. [1 ,2 ]
机构
[1] Univ Edinburgh, Inst Genet & Canc, Canc Res UK Scotland Ctr, Edinburgh EH4 2XR, Scotland
[2] Western Gen Hosp, Dept Colorectal Surg, Edinburgh EH4 2XU, Scotland
[3] Univ Edinburgh, Usher Inst, Ctr Global Hlth, Edinburgh EH4 2XR, Scotland
[4] Univ Glasgow, Sch Med Dent & Nursing, Glasgow City G12 8QQ, Scotland
[5] Queen Elizabeth Univ Hosp, Dept Surg, Glasgow City G51 4TF, Scotland
[6] Univ Edinburgh, Western Gen Hosp, Med Res Council Inst Genet & Canc, UK Colon Canc Genet Grp,Med Res Council Human Gene, Edinburgh EH4 2XU, Scotland
关键词
faecal immunochemical testing; FIT; colorectal cancer; CRC; colorectal diagnosis; bowel screening; OCCULT BLOOD-TEST; AVERAGE-RISK; POSITIVITY THRESHOLD; DIAGNOSTIC-ACCURACY; TEST FIT; NEOPLASIA; HEMOGLOBIN; NUMBER; POPULATION; PERFORMANCE;
D O I
10.3390/cancers16183199
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Simple Summary Faecal immunochemical testing is used to help aid the detection of bowel cancers and other serious bowel problems. It is a stool test that looks for non-visible blood. It has been shown that doing more than one test may improve the rate of detection of serious bowel problems; however, the evidence for this is not well described and has not been reviewed. We aimed to review the available data for using more than one test in different risk groups, exploring the effect on positivity and workload for additional tests along with assessing how well multiple tests work at detecting bowel cancer and other problems. The results of this are important as they help in the development of services to detect colorectal cancer.Abstract Background: Faecal immunochemical testing (FIT) is widely used in bowel screening programmes and assessing symptomatic patients for suspected colorectal cancer (CRC). The evidence for single test performance of FIT in both settings is considerable; however, the use of a repeat test to increase sensitivity remains uncertain. We aimed to review what increase in test positivity would be generated by additional FITs, whether a repeated FIT detects previously missed CRC and advanced colorectal neoplasia (ACRN), and to estimate the sensitivity of double-FIT strategies to diagnose CRC and ACRN. Methods: A systematic search of MEDLINE, EMBASE, and the Cochrane Central Register of Controlled Trials (CENTRAL) was performed using key search terms. Studies reporting the use of more than one FIT in the same screening round or planned assessment of a single symptomatic patient episode were included. Studies were categorised by the reported study population into asymptomatic, mixed (cohorts of combined asymptomatic, symptomatic, or high-risk surveillance), or symptomatic cohorts. Results: A total of 68 studies were included for analysis (39 asymptomatic, 21 mixed, 7 symptomatic, and 1 study with discrete asymptomatic and symptomatic data). At a threshold of 10 mu g Hb/g, the two-test positivity ranged between 8.1 and 34.5%, with an increase from the second test of 3-9.2 percentage points. Four out of five studies comparing one versus two tests for diagnosing CRC at 10 mu g Hb/g identified additional cases with the second test, with a minimum of 50% reduction in missed CRC. At a threshold of 20 mu g Hb/g, the second test increased the positivity by 1.3-6.7 percentage points, with a two-test positivity of between 5.1 and 25.0%. Using a threshold of 20 mu g Hb/g, five out of seven studies had a 25% reduction in missed CRC. A meta-analysis estimated the double-FIT sensitivity at 10 mu g Hb/g for CRC in mixed-risk and symptomatic cohorts to be 94% and 98%, respectively. Conclusions: Repeated use of FIT helps to diagnose more cases of CRC with a moderate increase in positivity. A double-FIT strategy at 10 mu g Hb/g in mixed and symptomatic cohorts has a very high sensitivity for CRC.
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