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Survival of patients with symptom- and screening-detected colorectal cancer
BACKGROUND: An increasing proportion of colorectal cancer (CRC) patients are diagnosed by screening rather than symptoms. AIMS: We aimed to assess and compare prognosis of patients with screen-detected CRC and symptom-detected CRC. METHODS: Overall and CRC specific mortality over a median follow-up...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5190129/ https://www.ncbi.nlm.nih.gov/pubmed/27213584 http://dx.doi.org/10.18632/oncotarget.9412 |
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author | Brenner, Hermann Jansen, Lina Ulrich, Alexis Chang-Claude, Jenny Hoffmeister, Michael |
author_facet | Brenner, Hermann Jansen, Lina Ulrich, Alexis Chang-Claude, Jenny Hoffmeister, Michael |
author_sort | Brenner, Hermann |
collection | PubMed |
description | BACKGROUND: An increasing proportion of colorectal cancer (CRC) patients are diagnosed by screening rather than symptoms. AIMS: We aimed to assess and compare prognosis of patients with screen-detected CRC and symptom-detected CRC. METHODS: Overall and CRC specific mortality over a median follow-up of 4.8 years was assessed according to mode of diagnosis (symptoms, screening colonoscopy, fecal occult blood test [FOBT], other) in a multi-center cohort of 2,450 CRC patients aged 50-79 years recruited in Germany in 2003-2010. RESULTS: 68%, 11% and 10% were detected by symptoms, screening colonoscopy and FOBT, respectively. The screen-detected cancers had a more favorable stage distribution than the symptom-detected cancers (68% versus 50% in stage I or II). Age- and sex adjusted hazard ratios (HRs) of total mortality with 95% confidence intervals (95% CIs) compared to symptom-detected cancers were 0.35 (0.24-0.50) and 0.36 (0.25-0.53) for screening colonoscopy and FOBT detected CRCs, respectively. HRs were only slightly attenuated and remained highly significant after adjustment for stage and multiple other covariates (0.50 (0.34-0.73) and 0.54 (0.37-0.80), respectively). Even stronger associations were seen for CRC specific mortality. Patients with screen-detected stage III CRC had as good CRC specific survival as patients with symptom-detected stage I or II CRC. CONCLUSIONS: Patients with screen-detected CRC have a very good prognosis far beyond the level explained by their more favorable stage distribution. Mode of detection is an important, easy-to-obtain proxy indicator for favorable diagnosis beyond earlier stage at diagnosis and as such may be useful for risk stratification in treatment decisions. |
format | Online Article Text |
id | pubmed-5190129 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-51901292017-01-05 Survival of patients with symptom- and screening-detected colorectal cancer Brenner, Hermann Jansen, Lina Ulrich, Alexis Chang-Claude, Jenny Hoffmeister, Michael Oncotarget Clinical Research Paper BACKGROUND: An increasing proportion of colorectal cancer (CRC) patients are diagnosed by screening rather than symptoms. AIMS: We aimed to assess and compare prognosis of patients with screen-detected CRC and symptom-detected CRC. METHODS: Overall and CRC specific mortality over a median follow-up of 4.8 years was assessed according to mode of diagnosis (symptoms, screening colonoscopy, fecal occult blood test [FOBT], other) in a multi-center cohort of 2,450 CRC patients aged 50-79 years recruited in Germany in 2003-2010. RESULTS: 68%, 11% and 10% were detected by symptoms, screening colonoscopy and FOBT, respectively. The screen-detected cancers had a more favorable stage distribution than the symptom-detected cancers (68% versus 50% in stage I or II). Age- and sex adjusted hazard ratios (HRs) of total mortality with 95% confidence intervals (95% CIs) compared to symptom-detected cancers were 0.35 (0.24-0.50) and 0.36 (0.25-0.53) for screening colonoscopy and FOBT detected CRCs, respectively. HRs were only slightly attenuated and remained highly significant after adjustment for stage and multiple other covariates (0.50 (0.34-0.73) and 0.54 (0.37-0.80), respectively). Even stronger associations were seen for CRC specific mortality. Patients with screen-detected stage III CRC had as good CRC specific survival as patients with symptom-detected stage I or II CRC. CONCLUSIONS: Patients with screen-detected CRC have a very good prognosis far beyond the level explained by their more favorable stage distribution. Mode of detection is an important, easy-to-obtain proxy indicator for favorable diagnosis beyond earlier stage at diagnosis and as such may be useful for risk stratification in treatment decisions. Impact Journals LLC 2016-05-17 /pmc/articles/PMC5190129/ /pubmed/27213584 http://dx.doi.org/10.18632/oncotarget.9412 Text en Copyright: © 2016 Brenner et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Clinical Research Paper Brenner, Hermann Jansen, Lina Ulrich, Alexis Chang-Claude, Jenny Hoffmeister, Michael Survival of patients with symptom- and screening-detected colorectal cancer |
title | Survival of patients with symptom- and screening-detected colorectal cancer |
title_full | Survival of patients with symptom- and screening-detected colorectal cancer |
title_fullStr | Survival of patients with symptom- and screening-detected colorectal cancer |
title_full_unstemmed | Survival of patients with symptom- and screening-detected colorectal cancer |
title_short | Survival of patients with symptom- and screening-detected colorectal cancer |
title_sort | survival of patients with symptom- and screening-detected colorectal cancer |
topic | Clinical Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5190129/ https://www.ncbi.nlm.nih.gov/pubmed/27213584 http://dx.doi.org/10.18632/oncotarget.9412 |
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