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The role of chemoprevention by selective cyclooxygenase-2 inhibitors in colorectal cancer patients - a population-based study
BACKGROUND: There are limited population-based studies focusing on the chemopreventive effects of selective cyclooxygenase-2 (COX-2) inhibitors against colorectal cancer. The purpose of this study is to assess the trends and dose–response effects of various medication possession ratios (MPR) of sele...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530430/ https://www.ncbi.nlm.nih.gov/pubmed/23217168 http://dx.doi.org/10.1186/1471-2407-12-582 |
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author | Yang, Yi-Hsin Yang, Yea-Huei Kao Cheng, Ching-Lan Ho, Pei-Shan Ko, Ying-Chin |
author_facet | Yang, Yi-Hsin Yang, Yea-Huei Kao Cheng, Ching-Lan Ho, Pei-Shan Ko, Ying-Chin |
author_sort | Yang, Yi-Hsin |
collection | PubMed |
description | BACKGROUND: There are limited population-based studies focusing on the chemopreventive effects of selective cyclooxygenase-2 (COX-2) inhibitors against colorectal cancer. The purpose of this study is to assess the trends and dose–response effects of various medication possession ratios (MPR) of selective COX-2 inhibitor used for chemoprevention of colorectal cancer. METHODS: A population-based case–control study was conducted using the Taiwan Health Insurance Research Database (NHIRD). The study comprised 21,460 colorectal cancer patients and 79,331 controls. The conditional logistic regression was applied to estimate the odds ratios (ORs) for COX-2 inhibitors used for several durations (5 years, 3 years, 1 year, 6 months and 3 months) prior to the index date. RESULTS: In patients receiving selective COX-2 inhibitors, the OR was 0.51 (95% CI=0.29~0.90, p=0.021) for an estimated 5-year period in developing colorectal cancer. ORs showing significant protection effects were found in 10% of MPRs for 5-year, 3-year, and 1-year usage. Risk reduction against colorectal cancer by selective COX-2 inhibitors was observed as early as 6 months after usage. CONCLUSION: Our results indicate that selective COX-2 inhibitors may reduce the development of colorectal cancer by at least 10% based on the MPRs evaluated. Given the limited number of clinical reports from general populations, our results add to the knowledge of chemopreventive effects of selective COX-2 inhibitors against cancer in individuals at no increased risk of colorectal cancer. |
format | Online Article Text |
id | pubmed-3530430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-35304302013-01-03 The role of chemoprevention by selective cyclooxygenase-2 inhibitors in colorectal cancer patients - a population-based study Yang, Yi-Hsin Yang, Yea-Huei Kao Cheng, Ching-Lan Ho, Pei-Shan Ko, Ying-Chin BMC Cancer Research Article BACKGROUND: There are limited population-based studies focusing on the chemopreventive effects of selective cyclooxygenase-2 (COX-2) inhibitors against colorectal cancer. The purpose of this study is to assess the trends and dose–response effects of various medication possession ratios (MPR) of selective COX-2 inhibitor used for chemoprevention of colorectal cancer. METHODS: A population-based case–control study was conducted using the Taiwan Health Insurance Research Database (NHIRD). The study comprised 21,460 colorectal cancer patients and 79,331 controls. The conditional logistic regression was applied to estimate the odds ratios (ORs) for COX-2 inhibitors used for several durations (5 years, 3 years, 1 year, 6 months and 3 months) prior to the index date. RESULTS: In patients receiving selective COX-2 inhibitors, the OR was 0.51 (95% CI=0.29~0.90, p=0.021) for an estimated 5-year period in developing colorectal cancer. ORs showing significant protection effects were found in 10% of MPRs for 5-year, 3-year, and 1-year usage. Risk reduction against colorectal cancer by selective COX-2 inhibitors was observed as early as 6 months after usage. CONCLUSION: Our results indicate that selective COX-2 inhibitors may reduce the development of colorectal cancer by at least 10% based on the MPRs evaluated. Given the limited number of clinical reports from general populations, our results add to the knowledge of chemopreventive effects of selective COX-2 inhibitors against cancer in individuals at no increased risk of colorectal cancer. BioMed Central 2012-12-06 /pmc/articles/PMC3530430/ /pubmed/23217168 http://dx.doi.org/10.1186/1471-2407-12-582 Text en Copyright ©2012 Yang et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Yang, Yi-Hsin Yang, Yea-Huei Kao Cheng, Ching-Lan Ho, Pei-Shan Ko, Ying-Chin The role of chemoprevention by selective cyclooxygenase-2 inhibitors in colorectal cancer patients - a population-based study |
title | The role of chemoprevention by selective cyclooxygenase-2 inhibitors in colorectal cancer patients - a population-based study |
title_full | The role of chemoprevention by selective cyclooxygenase-2 inhibitors in colorectal cancer patients - a population-based study |
title_fullStr | The role of chemoprevention by selective cyclooxygenase-2 inhibitors in colorectal cancer patients - a population-based study |
title_full_unstemmed | The role of chemoprevention by selective cyclooxygenase-2 inhibitors in colorectal cancer patients - a population-based study |
title_short | The role of chemoprevention by selective cyclooxygenase-2 inhibitors in colorectal cancer patients - a population-based study |
title_sort | role of chemoprevention by selective cyclooxygenase-2 inhibitors in colorectal cancer patients - a population-based study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3530430/ https://www.ncbi.nlm.nih.gov/pubmed/23217168 http://dx.doi.org/10.1186/1471-2407-12-582 |
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