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Faecal immunochemical testing in bowel cancer screening: Estimating outcomes for different diagnostic policies

OBJECTIVES: The National Health Service Bowel Cancer Screening Programme (NHS BCSP) in England has replaced guaiac faecal occult blood testing by faecal immunochemical testing (FIT). There is interest in fully exploiting FIT measures to improve bowel cancer (CRC) screening strategies. In this paper,...

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Autores principales: Li, Shuping J, Sharples, Linda D, Benton, Sally C, Blyuss, Oleg, Mathews, Christopher, Sasieni, Peter, Duffy, Stephen W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366184/
https://www.ncbi.nlm.nih.gov/pubmed/33342370
http://dx.doi.org/10.1177/0969141320980501
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author Li, Shuping J
Sharples, Linda D
Benton, Sally C
Blyuss, Oleg
Mathews, Christopher
Sasieni, Peter
Duffy, Stephen W
author_facet Li, Shuping J
Sharples, Linda D
Benton, Sally C
Blyuss, Oleg
Mathews, Christopher
Sasieni, Peter
Duffy, Stephen W
author_sort Li, Shuping J
collection PubMed
description OBJECTIVES: The National Health Service Bowel Cancer Screening Programme (NHS BCSP) in England has replaced guaiac faecal occult blood testing by faecal immunochemical testing (FIT). There is interest in fully exploiting FIT measures to improve bowel cancer (CRC) screening strategies. In this paper, we estimate the relationship of the quantitative haemoglobin concentration provided by FIT in faecal samples with underlying pathology. From this we estimate thresholds required for given levels of sensitivity to CRC and high-risk adenomas (HRA). METHODS: Data were collected from a pilot study of FIT in England in 2014, in which 27,238 participants completed a FIT. Those with a faecal haemoglobin concentration (f-Hb) of at least 20 µg/g were referred for further investigation, usually colonoscopy. Truncated regression models were used to explore the relationship between bowel pathology and FIT results. Regression results were applied to estimate sensitivity to different abnormalities for a number of thresholds. RESULTS: Participants with CRC and HRA had significantly higher f-Hb, and this remained unchanged after adjusting for age and sex. While a threshold of 20 μg/g was estimated to capture 82.2% of CRC and 64.0% of HRA, this would refer 7.8% of participants for colonoscopy. The current programme threshold used in England of 120 μg/g was estimated to identify 47.8% of CRC and 25.0% of HRA. CONCLUSIONS: Under the current diagnostic policy of dichotomising FIT results, a very low threshold would be required to achieve high sensitivity to CRC and HRA, which would place further strain on colonoscopy resources. The NHS BCSP in England might benefit from a diagnostic policy that makes greater use of the quantitative nature of FIT.
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spelling pubmed-83661842021-08-17 Faecal immunochemical testing in bowel cancer screening: Estimating outcomes for different diagnostic policies Li, Shuping J Sharples, Linda D Benton, Sally C Blyuss, Oleg Mathews, Christopher Sasieni, Peter Duffy, Stephen W J Med Screen Original Articles OBJECTIVES: The National Health Service Bowel Cancer Screening Programme (NHS BCSP) in England has replaced guaiac faecal occult blood testing by faecal immunochemical testing (FIT). There is interest in fully exploiting FIT measures to improve bowel cancer (CRC) screening strategies. In this paper, we estimate the relationship of the quantitative haemoglobin concentration provided by FIT in faecal samples with underlying pathology. From this we estimate thresholds required for given levels of sensitivity to CRC and high-risk adenomas (HRA). METHODS: Data were collected from a pilot study of FIT in England in 2014, in which 27,238 participants completed a FIT. Those with a faecal haemoglobin concentration (f-Hb) of at least 20 µg/g were referred for further investigation, usually colonoscopy. Truncated regression models were used to explore the relationship between bowel pathology and FIT results. Regression results were applied to estimate sensitivity to different abnormalities for a number of thresholds. RESULTS: Participants with CRC and HRA had significantly higher f-Hb, and this remained unchanged after adjusting for age and sex. While a threshold of 20 μg/g was estimated to capture 82.2% of CRC and 64.0% of HRA, this would refer 7.8% of participants for colonoscopy. The current programme threshold used in England of 120 μg/g was estimated to identify 47.8% of CRC and 25.0% of HRA. CONCLUSIONS: Under the current diagnostic policy of dichotomising FIT results, a very low threshold would be required to achieve high sensitivity to CRC and HRA, which would place further strain on colonoscopy resources. The NHS BCSP in England might benefit from a diagnostic policy that makes greater use of the quantitative nature of FIT. SAGE Publications 2020-12-20 2021-09 /pmc/articles/PMC8366184/ /pubmed/33342370 http://dx.doi.org/10.1177/0969141320980501 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution 4.0 License (https://creativecommons.org/licenses/by/4.0/) which permits any use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Li, Shuping J
Sharples, Linda D
Benton, Sally C
Blyuss, Oleg
Mathews, Christopher
Sasieni, Peter
Duffy, Stephen W
Faecal immunochemical testing in bowel cancer screening: Estimating outcomes for different diagnostic policies
title Faecal immunochemical testing in bowel cancer screening: Estimating outcomes for different diagnostic policies
title_full Faecal immunochemical testing in bowel cancer screening: Estimating outcomes for different diagnostic policies
title_fullStr Faecal immunochemical testing in bowel cancer screening: Estimating outcomes for different diagnostic policies
title_full_unstemmed Faecal immunochemical testing in bowel cancer screening: Estimating outcomes for different diagnostic policies
title_short Faecal immunochemical testing in bowel cancer screening: Estimating outcomes for different diagnostic policies
title_sort faecal immunochemical testing in bowel cancer screening: estimating outcomes for different diagnostic policies
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8366184/
https://www.ncbi.nlm.nih.gov/pubmed/33342370
http://dx.doi.org/10.1177/0969141320980501
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