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Screen-detected colorectal cancers are associated with an improved outcome compared with stage-matched interval cancers

BACKGROUND: Colorectal cancers (CRCs) detected through the NHS Bowel Cancer Screening Programme (BCSP) have been shown to have a more favourable outcome compared to non-screen-detected cancers. The aim was to identify whether this was solely due to the earlier stage shift of these cancers, or whethe...

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Autores principales: Gill, M D, Bramble, M G, Hull, M A, Mills, S J, Morris, E, Bradburn, D M, Bury, Y, Parker, C E, Lee, T J W, Rees, C J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260027/
https://www.ncbi.nlm.nih.gov/pubmed/25247322
http://dx.doi.org/10.1038/bjc.2014.498
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author Gill, M D
Bramble, M G
Hull, M A
Mills, S J
Morris, E
Bradburn, D M
Bury, Y
Parker, C E
Lee, T J W
Rees, C J
author_facet Gill, M D
Bramble, M G
Hull, M A
Mills, S J
Morris, E
Bradburn, D M
Bury, Y
Parker, C E
Lee, T J W
Rees, C J
author_sort Gill, M D
collection PubMed
description BACKGROUND: Colorectal cancers (CRCs) detected through the NHS Bowel Cancer Screening Programme (BCSP) have been shown to have a more favourable outcome compared to non-screen-detected cancers. The aim was to identify whether this was solely due to the earlier stage shift of these cancers, or whether other factors were involved. METHODS: A combination of a regional CRC registry (Northern Colorectal Cancer Audit Group) and the BCSP database were used to identify screen-detected and interval cancers (diagnosed after a negative faecal occult blood test, before the next screening round), diagnosed between April 2007 and March 2010, within the North East of England. For each Dukes' stage, patient demographics, tumour characteristics, and survival rates were compared between these two groups. RESULTS: Overall, 322 screen-detected cancers were compared against 192 interval cancers. Screen-detected Dukes' C and D CRCs had a superior survival rate compared with interval cancers (P=0.014 and P=0.04, respectively). Cox proportional hazards regression showed that Dukes' stage, tumour location, and diagnostic group (HR 0.45, 95% CI 0.29–0.69, P<0.001 for screen-detected CRCs) were all found to have a significant impact on the survival of patients. CONCLUSIONS: The improved survival of screen-detected over interval cancers for stages C and D suggest that there may be a biological difference in the cancers in each group. Although lead-time bias may have a role, this may be related to a tumour's propensity to bleed and therefore may reflect detection through current screening tests.
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spelling pubmed-42600272015-11-25 Screen-detected colorectal cancers are associated with an improved outcome compared with stage-matched interval cancers Gill, M D Bramble, M G Hull, M A Mills, S J Morris, E Bradburn, D M Bury, Y Parker, C E Lee, T J W Rees, C J Br J Cancer Clinical Study BACKGROUND: Colorectal cancers (CRCs) detected through the NHS Bowel Cancer Screening Programme (BCSP) have been shown to have a more favourable outcome compared to non-screen-detected cancers. The aim was to identify whether this was solely due to the earlier stage shift of these cancers, or whether other factors were involved. METHODS: A combination of a regional CRC registry (Northern Colorectal Cancer Audit Group) and the BCSP database were used to identify screen-detected and interval cancers (diagnosed after a negative faecal occult blood test, before the next screening round), diagnosed between April 2007 and March 2010, within the North East of England. For each Dukes' stage, patient demographics, tumour characteristics, and survival rates were compared between these two groups. RESULTS: Overall, 322 screen-detected cancers were compared against 192 interval cancers. Screen-detected Dukes' C and D CRCs had a superior survival rate compared with interval cancers (P=0.014 and P=0.04, respectively). Cox proportional hazards regression showed that Dukes' stage, tumour location, and diagnostic group (HR 0.45, 95% CI 0.29–0.69, P<0.001 for screen-detected CRCs) were all found to have a significant impact on the survival of patients. CONCLUSIONS: The improved survival of screen-detected over interval cancers for stages C and D suggest that there may be a biological difference in the cancers in each group. Although lead-time bias may have a role, this may be related to a tumour's propensity to bleed and therefore may reflect detection through current screening tests. Nature Publishing Group 2014-11-25 2014-09-23 /pmc/articles/PMC4260027/ /pubmed/25247322 http://dx.doi.org/10.1038/bjc.2014.498 Text en Copyright © 2014 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Clinical Study
Gill, M D
Bramble, M G
Hull, M A
Mills, S J
Morris, E
Bradburn, D M
Bury, Y
Parker, C E
Lee, T J W
Rees, C J
Screen-detected colorectal cancers are associated with an improved outcome compared with stage-matched interval cancers
title Screen-detected colorectal cancers are associated with an improved outcome compared with stage-matched interval cancers
title_full Screen-detected colorectal cancers are associated with an improved outcome compared with stage-matched interval cancers
title_fullStr Screen-detected colorectal cancers are associated with an improved outcome compared with stage-matched interval cancers
title_full_unstemmed Screen-detected colorectal cancers are associated with an improved outcome compared with stage-matched interval cancers
title_short Screen-detected colorectal cancers are associated with an improved outcome compared with stage-matched interval cancers
title_sort screen-detected colorectal cancers are associated with an improved outcome compared with stage-matched interval cancers
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4260027/
https://www.ncbi.nlm.nih.gov/pubmed/25247322
http://dx.doi.org/10.1038/bjc.2014.498
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