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Cost-effectiveness analysis of colorectal cancer screening with stool DNA testing in intermediate-incidence countries
BACKGROUND: The aim of this study is to compare the cost-effectiveness of screening with stool DNA testing with that of screening with other tools (annual fecal occult blood testing, flexible sigmoidoscopy every 5 years, and colonoscopy every 10 years) or not screening at all. METHODS: We developed...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1525200/ https://www.ncbi.nlm.nih.gov/pubmed/16723013 http://dx.doi.org/10.1186/1471-2407-6-136 |
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author | Wu, Grace Hui-Min Wang, Yi-Ming Yen, Amy Ming-Fang Wong, Jau-Min Lai, Hsin-Chih Warwick, Jane Chen, Tony Hsiu-Hsi |
author_facet | Wu, Grace Hui-Min Wang, Yi-Ming Yen, Amy Ming-Fang Wong, Jau-Min Lai, Hsin-Chih Warwick, Jane Chen, Tony Hsiu-Hsi |
author_sort | Wu, Grace Hui-Min |
collection | PubMed |
description | BACKGROUND: The aim of this study is to compare the cost-effectiveness of screening with stool DNA testing with that of screening with other tools (annual fecal occult blood testing, flexible sigmoidoscopy every 5 years, and colonoscopy every 10 years) or not screening at all. METHODS: We developed a Markov model to evaluate the above screening strategies in the general population 50 to 75 years of age in Taiwan. Sensitivity analyses were performed to assess the influence of various parameters on the cost-effectiveness of screening. A third-party payer perspective was adopted and the cost of $13,000 per life-year saved (which is roughly the per capita GNP of Taiwan in 2003) was chosen as the ceiling ratio for assessing whether the program is cost-effective. RESULTS: Stool DNA testing every three, five, and ten years can reduce colorectal cancer mortality by 22%, 15%, and 9%, respectively. The associated incremental costs were $9,794, $9,335, and $7,717, per life-year saved when compared with no screening. Stool DNA testing strategies were the least cost-effective with the cost per stool DNA test, referral rate with diagnostic colonoscopy, prevalence of large adenoma, and discount rate being the most influential parameters. CONCLUSION: In countries with a low or intermediate incidence of colorectal cancer, stool DNA testing is less cost-effective than the other currently recommended strategies for population-based screening, particularly targeting at asymptomatic subjects. |
format | Text |
id | pubmed-1525200 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-15252002006-08-02 Cost-effectiveness analysis of colorectal cancer screening with stool DNA testing in intermediate-incidence countries Wu, Grace Hui-Min Wang, Yi-Ming Yen, Amy Ming-Fang Wong, Jau-Min Lai, Hsin-Chih Warwick, Jane Chen, Tony Hsiu-Hsi BMC Cancer Research Article BACKGROUND: The aim of this study is to compare the cost-effectiveness of screening with stool DNA testing with that of screening with other tools (annual fecal occult blood testing, flexible sigmoidoscopy every 5 years, and colonoscopy every 10 years) or not screening at all. METHODS: We developed a Markov model to evaluate the above screening strategies in the general population 50 to 75 years of age in Taiwan. Sensitivity analyses were performed to assess the influence of various parameters on the cost-effectiveness of screening. A third-party payer perspective was adopted and the cost of $13,000 per life-year saved (which is roughly the per capita GNP of Taiwan in 2003) was chosen as the ceiling ratio for assessing whether the program is cost-effective. RESULTS: Stool DNA testing every three, five, and ten years can reduce colorectal cancer mortality by 22%, 15%, and 9%, respectively. The associated incremental costs were $9,794, $9,335, and $7,717, per life-year saved when compared with no screening. Stool DNA testing strategies were the least cost-effective with the cost per stool DNA test, referral rate with diagnostic colonoscopy, prevalence of large adenoma, and discount rate being the most influential parameters. CONCLUSION: In countries with a low or intermediate incidence of colorectal cancer, stool DNA testing is less cost-effective than the other currently recommended strategies for population-based screening, particularly targeting at asymptomatic subjects. BioMed Central 2006-05-24 /pmc/articles/PMC1525200/ /pubmed/16723013 http://dx.doi.org/10.1186/1471-2407-6-136 Text en Copyright © 2006 Wu 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 Wu, Grace Hui-Min Wang, Yi-Ming Yen, Amy Ming-Fang Wong, Jau-Min Lai, Hsin-Chih Warwick, Jane Chen, Tony Hsiu-Hsi Cost-effectiveness analysis of colorectal cancer screening with stool DNA testing in intermediate-incidence countries |
title | Cost-effectiveness analysis of colorectal cancer screening with stool DNA testing in intermediate-incidence countries |
title_full | Cost-effectiveness analysis of colorectal cancer screening with stool DNA testing in intermediate-incidence countries |
title_fullStr | Cost-effectiveness analysis of colorectal cancer screening with stool DNA testing in intermediate-incidence countries |
title_full_unstemmed | Cost-effectiveness analysis of colorectal cancer screening with stool DNA testing in intermediate-incidence countries |
title_short | Cost-effectiveness analysis of colorectal cancer screening with stool DNA testing in intermediate-incidence countries |
title_sort | cost-effectiveness analysis of colorectal cancer screening with stool dna testing in intermediate-incidence countries |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1525200/ https://www.ncbi.nlm.nih.gov/pubmed/16723013 http://dx.doi.org/10.1186/1471-2407-6-136 |
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