Choice of faecal immunochemical test matters: comparison of OC-Sensor and HM-JACKarc, in the assessment of patients at high risk of colorectal cancer

Author:

Chapman Caroline J.12,Banerjea Ayan3,Humes David J345,Allen Jaren2ORCID,Oliver Simon6,Ford Abby1,Hardy Katie1,Djedovic Natasha1,Logan Richard F.15,Morling Joanne R.145

Affiliation:

1. Eastern Hub, Bowel Cancer Screening Programme , A Floor West Block, QMC Campus, Nottingham University Hospitals NHS Trust , Nottingham , UK

2. Division of Cancer and Stem Cells, School of Medicine , Room W/D3, D Floor, West Block, Queen’s Medical Centre , Nottingham , UK

3. Nottingham Colorectal Service , E Floor West Block, QMC Campus, Nottingham University Hospitals NHS Trust , Nottingham , UK

4. NIHR Nottingham Biomedical Research Centre , Nottingham University Hospitals NHS Trust and the University of Nottingham , Nottingham , UK

5. Division of Epidemiology and Public Health, School of Medicine , University of Nottingham , Clinical Sciences Building 2, City Hospital , Nottingham , UK

6. Nottingham City Clinical Commissioning Group , Nottingham , UK

Abstract

Abstract Objectives Currently, NICE recommends the use of faecal immunochemical test (FIT) at faecal haemoglobin concentrations (f-Hb) of 10 μg Hb/g faeces to stratify for colorectal cancer (CRC) risk in symptomatic populations. This f-Hb cut-off is advised across all analysers, despite the fact that a direct comparison of analyser performance, in a clinical setting, has not been performed. Methods Two specimen collection devices (OC-Sensor, OC-S; HM-JACKarc, HM-J) were sent to 914 consecutive individuals referred for follow up due to their increased risk of CRC. Agreement of f-Hb around cut-offs of 4, 10 and 150 µg Hb/g faeces and CRC detection rates were assessed. Two OC-S devices were sent to a further 114 individuals, for within test comparisons. Results A total of 732 (80.1%) individuals correctly completed and returned two different FIT devices, with 38 (5.2%) CRCs detected. Median f-Hb for individuals diagnosed with and without CRC were 258.5 and 1.8 µg Hb/g faeces for OC-S and 318.1 and 1.0 µg Hb/g faeces for HM-J respectively. Correlation of f-Hb results between OC-S/HM-J over the full range was rho=0.74, p<0.001. Using a f-Hb of 4 µg Hb/g faeces for both tests found an agreement of 88.1%, at 10 µg Hb/g faeces 91.7% and at 150 µg Hb/g faeces 96.3%. A total of 114 individuals completed and returned two OC-S devices; correlation across the full range was rho=0.98, p<0.001. Conclusions We found large variations in f-Hb when different FIT devices were used, but a smaller variation when the same FIT device was used. Our data suggest that analyser-specific f-Hb cut-offs are applied with regard to clinical decision making, especially at lower f-Hb.

Funder

National Institute for Health Research

Medical Research Council Clinician Scientist Fellowship

Publisher

Walter de Gruyter GmbH

Subject

Biochemistry (medical),Clinical Biochemistry,General Medicine

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