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Colorectal Cancer Risk in Women with Gynecologic Cancers—A Population Retrospective Cohort Study
We conducted a retrospective cohort study to evaluate the subsequent colorectal cancer (CRC) risk for women with gynecologic malignancy using insurance claims data of Taiwan. We identified patients who survived cervical cancer (N = 25,370), endometrial cancer (N = 8149) and ovarian cancer (N = 7933)...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8303695/ https://www.ncbi.nlm.nih.gov/pubmed/34300293 http://dx.doi.org/10.3390/jcm10143127 |
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author | Liao, Szu-Chia Yeh, Hong-Zen Chang, Chi-Sen Chen, Wei-Chih Muo, Chih-Hsin Sung, Fung-Chang |
author_facet | Liao, Szu-Chia Yeh, Hong-Zen Chang, Chi-Sen Chen, Wei-Chih Muo, Chih-Hsin Sung, Fung-Chang |
author_sort | Liao, Szu-Chia |
collection | PubMed |
description | We conducted a retrospective cohort study to evaluate the subsequent colorectal cancer (CRC) risk for women with gynecologic malignancy using insurance claims data of Taiwan. We identified patients who survived cervical cancer (N = 25,370), endometrial cancer (N = 8149) and ovarian cancer (N = 7933) newly diagnosed from 1998 to 2010, and randomly selected comparisons (N = 165,808) without cancer, matched by age and diagnosis date. By the end of 2011, the incidence and hazard ratio (HR) of CRC were estimated. We found that CRC incidence rates were 1.26-, 2.20-, and 1.61-fold higher in women with cervical, endometrial and ovarian cancers, respectively, than in comparisons (1.09/1000 person–years). The CRC incidence increased with age. Higher adjusted HRs of CRC appeared within 3 years for women with endometrial and ovarian cancers, but not until the 4th to 7th years of follow up for cervical cancer survivals. Cancer treatments could reduce CRC risks, but not significantly. However, ovarian cancer patients receiving surgery alone had an incidence of 3.33/1000 person–years for CRC with an adjusted HR of 3.79 (95% CI 1.11–12.9) compared to patients without any treatment. In conclusion, gynecologic cancer patients are at an increased risk of developing CRC, sooner for those with endometrial or ovarian cancer than those with cervical cancer. |
format | Online Article Text |
id | pubmed-8303695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83036952021-07-25 Colorectal Cancer Risk in Women with Gynecologic Cancers—A Population Retrospective Cohort Study Liao, Szu-Chia Yeh, Hong-Zen Chang, Chi-Sen Chen, Wei-Chih Muo, Chih-Hsin Sung, Fung-Chang J Clin Med Article We conducted a retrospective cohort study to evaluate the subsequent colorectal cancer (CRC) risk for women with gynecologic malignancy using insurance claims data of Taiwan. We identified patients who survived cervical cancer (N = 25,370), endometrial cancer (N = 8149) and ovarian cancer (N = 7933) newly diagnosed from 1998 to 2010, and randomly selected comparisons (N = 165,808) without cancer, matched by age and diagnosis date. By the end of 2011, the incidence and hazard ratio (HR) of CRC were estimated. We found that CRC incidence rates were 1.26-, 2.20-, and 1.61-fold higher in women with cervical, endometrial and ovarian cancers, respectively, than in comparisons (1.09/1000 person–years). The CRC incidence increased with age. Higher adjusted HRs of CRC appeared within 3 years for women with endometrial and ovarian cancers, but not until the 4th to 7th years of follow up for cervical cancer survivals. Cancer treatments could reduce CRC risks, but not significantly. However, ovarian cancer patients receiving surgery alone had an incidence of 3.33/1000 person–years for CRC with an adjusted HR of 3.79 (95% CI 1.11–12.9) compared to patients without any treatment. In conclusion, gynecologic cancer patients are at an increased risk of developing CRC, sooner for those with endometrial or ovarian cancer than those with cervical cancer. MDPI 2021-07-15 /pmc/articles/PMC8303695/ /pubmed/34300293 http://dx.doi.org/10.3390/jcm10143127 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Liao, Szu-Chia Yeh, Hong-Zen Chang, Chi-Sen Chen, Wei-Chih Muo, Chih-Hsin Sung, Fung-Chang Colorectal Cancer Risk in Women with Gynecologic Cancers—A Population Retrospective Cohort Study |
title | Colorectal Cancer Risk in Women with Gynecologic Cancers—A Population Retrospective Cohort Study |
title_full | Colorectal Cancer Risk in Women with Gynecologic Cancers—A Population Retrospective Cohort Study |
title_fullStr | Colorectal Cancer Risk in Women with Gynecologic Cancers—A Population Retrospective Cohort Study |
title_full_unstemmed | Colorectal Cancer Risk in Women with Gynecologic Cancers—A Population Retrospective Cohort Study |
title_short | Colorectal Cancer Risk in Women with Gynecologic Cancers—A Population Retrospective Cohort Study |
title_sort | colorectal cancer risk in women with gynecologic cancers—a population retrospective cohort study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8303695/ https://www.ncbi.nlm.nih.gov/pubmed/34300293 http://dx.doi.org/10.3390/jcm10143127 |
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