A comparison of the faecal haemoglobin concentrations and diagnostic accuracy in patients suspected with colorectal cancer and serious bowel disease as reported on four different faecal immunochemical test systems

Author:

Benton Sally C.12ORCID,Piggott Carolyn2ORCID,Zahoor Zahida2ORCID,O’Driscoll Shane2ORCID,Fraser Callum G.3ORCID,D’Souza Nigel4,Chen Michelle5,Georgiou Delisle Theo4,Abulafi Muti4

Affiliation:

1. Clinical Biochemistry , Royal Surrey County Hospital, Berkshire and Surrey Pathology Services , Guildford , Surrey , UK

2. NHS Bowel Cancer Screening South of England Hub , Berkshire and Surrey Pathology Services , Guildford , Surrey , UK

3. Centre for Research into Cancer Prevention and Screening, Population Health and Genomics, School of Medicine , University of Dundee , Scotland , UK

4. Department of Colorectal Surgery , Croydon University Hospital , Croydon , UK

5. Research and Development , RM Partners, the West London Cancer Alliance , London , UK

Abstract

Abstract Objectives Faecal immunochemical tests for haemoglobin (FIT) are used in colorectal cancer (CRC) screening programmes and to triage patients presenting with symptoms suggestive of CRC for further bowel investigations. There are a number of quantitative FIT analytical systems available. Currently, there is no harmonisation or standardisation of FIT methods. The aim of the study was to assess the comparability of numerical faecal haemoglobin concentrations (f-Hb) obtained with four quantitative FIT systems and the diagnostic accuracy at different f-Hb thresholds. Methods A subgroup of the National Institute for Health and Care Excellence (NICE) FIT study, a multicentre, prospective diagnostic accuracy study were sent four FIT specimen collection devices from four different FIT systems or two FIT devices for one FIT system. Faecal samples were examined and analysis of results carried out to assess difference between methods at thresholds of limit of detection (LoD), 10 µg haemoglobin/g faeces (µg/g) and 100 μg/g. Results 233 patients returned specimen collection devices for examination on four different systems; 189 patients returned two FIT kits for one system. At a threshold of 100 μg/g the sensitivity is the same for all methods. At lower thresholds of LoD and 10 μg/g differences were observed between systems in terms of patients who would be referred and diagnostic accuracies. Conclusions The lack of standardisation or harmonisation of FIT means that differences are observed in f-Hb generated on different systems. Further work is required to understand the clinical impact of these differences and to minimise them.

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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