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Proximal shift of colorectal cancer with increasing age in different ethnicities

BACKGROUND: Studies have indicated a variation in colon cancer pathology with increased age. More findings have also suggested differences in genetics, biology, and demography in terms of ethnicity. Large-scale studies closely examining tumor location shift with aging and ethnicity are scarce. OBJEC...

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Autores principales: Yang, Lin, Xiong, Zhenchong, He, Wenzhuo, Xie, Kunqian, Liu, Shousheng, Kong, Pengfei, Jiang, Chang, Guo, Guifang, Xia, Liangping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101018/
https://www.ncbi.nlm.nih.gov/pubmed/30147365
http://dx.doi.org/10.2147/CMAR.S166548
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author Yang, Lin
Xiong, Zhenchong
He, Wenzhuo
Xie, Kunqian
Liu, Shousheng
Kong, Pengfei
Jiang, Chang
Guo, Guifang
Xia, Liangping
author_facet Yang, Lin
Xiong, Zhenchong
He, Wenzhuo
Xie, Kunqian
Liu, Shousheng
Kong, Pengfei
Jiang, Chang
Guo, Guifang
Xia, Liangping
author_sort Yang, Lin
collection PubMed
description BACKGROUND: Studies have indicated a variation in colon cancer pathology with increased age. More findings have also suggested differences in genetics, biology, and demography in terms of ethnicity. Large-scale studies closely examining tumor location shift with aging and ethnicity are scarce. OBJECTIVE: We compared the tumor location shift with aging and the difference in survival based on tumor location by age group among the African-American, White, and Asian/Pacific Islander patients with colorectal cancer. MATERIALS AND METHODS: We collected 270,390 cases from the Surveillance, Epidemiology, and End Results database between 2004 and 2014. Ethnicity distribution between younger (age <70 years) and older (age ≥70 years) patients was analyzed using univariate and multivariate logistic regression. The Kaplan–Meier method was used to compare the tumor location survival difference in the African-American, White, and Asian/Pacific Islander patients. RESULTS: Larger tumors, female sex, M0, advanced N stage, no treatment, moderate to poor differentiation, total number of lymph nodes evaluated >12, and right-sided colon cancer were more common in patients aged ≥70 years. More adverse prognosis was found in younger patients compared to older patients. Tumor location frequency differed based on age; the most pronounced differences were found in White patients. The right-sided colon cancer survival inferiority was present only in White patients. CONCLUSION: Our findings support the premise of etiological and carcinogenic differences based on tumor location and between younger and older patients.
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spelling pubmed-61010182018-08-24 Proximal shift of colorectal cancer with increasing age in different ethnicities Yang, Lin Xiong, Zhenchong He, Wenzhuo Xie, Kunqian Liu, Shousheng Kong, Pengfei Jiang, Chang Guo, Guifang Xia, Liangping Cancer Manag Res Original Research BACKGROUND: Studies have indicated a variation in colon cancer pathology with increased age. More findings have also suggested differences in genetics, biology, and demography in terms of ethnicity. Large-scale studies closely examining tumor location shift with aging and ethnicity are scarce. OBJECTIVE: We compared the tumor location shift with aging and the difference in survival based on tumor location by age group among the African-American, White, and Asian/Pacific Islander patients with colorectal cancer. MATERIALS AND METHODS: We collected 270,390 cases from the Surveillance, Epidemiology, and End Results database between 2004 and 2014. Ethnicity distribution between younger (age <70 years) and older (age ≥70 years) patients was analyzed using univariate and multivariate logistic regression. The Kaplan–Meier method was used to compare the tumor location survival difference in the African-American, White, and Asian/Pacific Islander patients. RESULTS: Larger tumors, female sex, M0, advanced N stage, no treatment, moderate to poor differentiation, total number of lymph nodes evaluated >12, and right-sided colon cancer were more common in patients aged ≥70 years. More adverse prognosis was found in younger patients compared to older patients. Tumor location frequency differed based on age; the most pronounced differences were found in White patients. The right-sided colon cancer survival inferiority was present only in White patients. CONCLUSION: Our findings support the premise of etiological and carcinogenic differences based on tumor location and between younger and older patients. Dove Medical Press 2018-08-15 /pmc/articles/PMC6101018/ /pubmed/30147365 http://dx.doi.org/10.2147/CMAR.S166548 Text en © 2018 Yang et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Yang, Lin
Xiong, Zhenchong
He, Wenzhuo
Xie, Kunqian
Liu, Shousheng
Kong, Pengfei
Jiang, Chang
Guo, Guifang
Xia, Liangping
Proximal shift of colorectal cancer with increasing age in different ethnicities
title Proximal shift of colorectal cancer with increasing age in different ethnicities
title_full Proximal shift of colorectal cancer with increasing age in different ethnicities
title_fullStr Proximal shift of colorectal cancer with increasing age in different ethnicities
title_full_unstemmed Proximal shift of colorectal cancer with increasing age in different ethnicities
title_short Proximal shift of colorectal cancer with increasing age in different ethnicities
title_sort proximal shift of colorectal cancer with increasing age in different ethnicities
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6101018/
https://www.ncbi.nlm.nih.gov/pubmed/30147365
http://dx.doi.org/10.2147/CMAR.S166548
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