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Effect of low-dose aspirin use on survival of patients with gastrointestinal malignancies; an observational study
BACKGROUND: Previous studies suggested a relationship between aspirin use and mortality reduction. The mechanism for the effect of aspirin on cancer outcomes remains unclear. The aim of this study was to evaluate aspirin use and survival in patients with gastrointestinal tract cancer. METHODS: Patie...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294482/ https://www.ncbi.nlm.nih.gov/pubmed/28072768 http://dx.doi.org/10.1038/bjc.2016.425 |
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author | Frouws, M A Bastiaannet, E Langley, R E Chia, W K van Herk-Sukel, M P P Lemmens, V E P P Putter, H Hartgrink, H H Bonsing, B A Van de Velde, C J H Portielje, J E A Liefers, G J |
author_facet | Frouws, M A Bastiaannet, E Langley, R E Chia, W K van Herk-Sukel, M P P Lemmens, V E P P Putter, H Hartgrink, H H Bonsing, B A Van de Velde, C J H Portielje, J E A Liefers, G J |
author_sort | Frouws, M A |
collection | PubMed |
description | BACKGROUND: Previous studies suggested a relationship between aspirin use and mortality reduction. The mechanism for the effect of aspirin on cancer outcomes remains unclear. The aim of this study was to evaluate aspirin use and survival in patients with gastrointestinal tract cancer. METHODS: Patients with gastrointestinal tract cancer diagnosed between 1998 and 2011 were included. The population-based Eindhoven Cancer Registry was linked to drug-dispensing data from the PHARMO Database Network. The association between aspirin use after diagnosis and overall survival was analysed using Cox regression models. RESULTS: In total, 13 715 patients were diagnosed with gastrointestinal cancer. A total of 1008 patients were identified as aspirin users, and 8278 patients were identified as nonusers. The adjusted hazard ratio for aspirin users vs nonusers was 0.52 (95% CI 0.44–0.63). A significant association between aspirin use and survival was observed for patients with oesophageal, hepatobiliary and colorectal cancer. CONCLUSIONS: Post-diagnosis use of aspirin in patients with gastrointestinal tract malignancies is associated with increased survival in cancers with different sites of origin and biology. This adds weight to the hypothesis that the anti-cancer effects of aspirin are not tumour-site specific and may be modulated through the tumour micro-environment. |
format | Online Article Text |
id | pubmed-5294482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52944822018-01-31 Effect of low-dose aspirin use on survival of patients with gastrointestinal malignancies; an observational study Frouws, M A Bastiaannet, E Langley, R E Chia, W K van Herk-Sukel, M P P Lemmens, V E P P Putter, H Hartgrink, H H Bonsing, B A Van de Velde, C J H Portielje, J E A Liefers, G J Br J Cancer Epidemiology BACKGROUND: Previous studies suggested a relationship between aspirin use and mortality reduction. The mechanism for the effect of aspirin on cancer outcomes remains unclear. The aim of this study was to evaluate aspirin use and survival in patients with gastrointestinal tract cancer. METHODS: Patients with gastrointestinal tract cancer diagnosed between 1998 and 2011 were included. The population-based Eindhoven Cancer Registry was linked to drug-dispensing data from the PHARMO Database Network. The association between aspirin use after diagnosis and overall survival was analysed using Cox regression models. RESULTS: In total, 13 715 patients were diagnosed with gastrointestinal cancer. A total of 1008 patients were identified as aspirin users, and 8278 patients were identified as nonusers. The adjusted hazard ratio for aspirin users vs nonusers was 0.52 (95% CI 0.44–0.63). A significant association between aspirin use and survival was observed for patients with oesophageal, hepatobiliary and colorectal cancer. CONCLUSIONS: Post-diagnosis use of aspirin in patients with gastrointestinal tract malignancies is associated with increased survival in cancers with different sites of origin and biology. This adds weight to the hypothesis that the anti-cancer effects of aspirin are not tumour-site specific and may be modulated through the tumour micro-environment. Nature Publishing Group 2017-01-31 2017-01-10 /pmc/articles/PMC5294482/ /pubmed/28072768 http://dx.doi.org/10.1038/bjc.2016.425 Text en Copyright © 2017 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/4.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 4.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/4.0/ |
spellingShingle | Epidemiology Frouws, M A Bastiaannet, E Langley, R E Chia, W K van Herk-Sukel, M P P Lemmens, V E P P Putter, H Hartgrink, H H Bonsing, B A Van de Velde, C J H Portielje, J E A Liefers, G J Effect of low-dose aspirin use on survival of patients with gastrointestinal malignancies; an observational study |
title | Effect of low-dose aspirin use on survival of patients with gastrointestinal malignancies; an observational study |
title_full | Effect of low-dose aspirin use on survival of patients with gastrointestinal malignancies; an observational study |
title_fullStr | Effect of low-dose aspirin use on survival of patients with gastrointestinal malignancies; an observational study |
title_full_unstemmed | Effect of low-dose aspirin use on survival of patients with gastrointestinal malignancies; an observational study |
title_short | Effect of low-dose aspirin use on survival of patients with gastrointestinal malignancies; an observational study |
title_sort | effect of low-dose aspirin use on survival of patients with gastrointestinal malignancies; an observational study |
topic | Epidemiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5294482/ https://www.ncbi.nlm.nih.gov/pubmed/28072768 http://dx.doi.org/10.1038/bjc.2016.425 |
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