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Population-based analysis on predictors for lymph node metastasis in T1 colon cancer

BACKGROUND: In this study, we aimed to identify independent predictive factors for lymph node metastasis (LNM) in T1 colon cancer. METHODS: Data of 8056 eligible patients were retrospectively collected from the Surveillance, Epidemiology, and End Results (SEER) database during 2004–2012. We performe...

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Autores principales: Xu, Xin, Zhang, Chihao, Ni, Xiaochun, Wu, Jugang, Pan, Chunpeng, Wang, Shoulian, Yu, Jiwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395001/
https://www.ncbi.nlm.nih.gov/pubmed/31620912
http://dx.doi.org/10.1007/s00464-019-07192-0
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author Xu, Xin
Zhang, Chihao
Ni, Xiaochun
Wu, Jugang
Pan, Chunpeng
Wang, Shoulian
Yu, Jiwei
author_facet Xu, Xin
Zhang, Chihao
Ni, Xiaochun
Wu, Jugang
Pan, Chunpeng
Wang, Shoulian
Yu, Jiwei
author_sort Xu, Xin
collection PubMed
description BACKGROUND: In this study, we aimed to identify independent predictive factors for lymph node metastasis (LNM) in T1 colon cancer. METHODS: Data of 8056 eligible patients were retrospectively collected from the Surveillance, Epidemiology, and End Results (SEER) database during 2004–2012. We performed logistic regression analysis to identify predictive factors for LNM. Both unadjusted and adjusted Cox regression analyses were used to determine the association between LNM and patient survival. Finally, we used competing risks analysis and the cumulative incidence function (CIF) to further confirm the prognostic role of LNM in cancer-specific survival (CSS). RESULTS: The overall risk of LNM in patients with T1 colon cancer was 12.0% (N = 967). Adjusted logistic regression models revealed that mucinous carcinoma [odds ratio (OR) = 2.26, P < 0.001], moderately differentiated (OR 1.74, P < 0.001), poorly differentiated (OR 5.16, P < 0.001), and undifferentiated carcinoma (OR 3.01, P = 0.003); older age (OR 0.66, P < 0.001 for age 65–79 years, OR 0.44, P < 0.001 for age over 80 years); and carcinoma located in the ascending colon (OR 0.77, P = 0.018) and sigmoid colon (OR 1.24, P = 0.014) were independent predictive factors for LNM. Adjusted Cox regression analysis showed that positive lymph node involvement was significantly associated with CSS [hazard ratio (HR) = 3.02, P < 0.001], which was further robustly confirmed using a competing risks model and the CIF. CONCLUSIONS: This population-based study showed that mucinous carcinoma, tumor grade, age, and primary tumor location were independent predictive factors for LNM in T1 colon cancer. The risk of LNM should be carefully evaluated in patients with T1 colon cancer, before clinical management.
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spelling pubmed-73950012020-08-18 Population-based analysis on predictors for lymph node metastasis in T1 colon cancer Xu, Xin Zhang, Chihao Ni, Xiaochun Wu, Jugang Pan, Chunpeng Wang, Shoulian Yu, Jiwei Surg Endosc Article BACKGROUND: In this study, we aimed to identify independent predictive factors for lymph node metastasis (LNM) in T1 colon cancer. METHODS: Data of 8056 eligible patients were retrospectively collected from the Surveillance, Epidemiology, and End Results (SEER) database during 2004–2012. We performed logistic regression analysis to identify predictive factors for LNM. Both unadjusted and adjusted Cox regression analyses were used to determine the association between LNM and patient survival. Finally, we used competing risks analysis and the cumulative incidence function (CIF) to further confirm the prognostic role of LNM in cancer-specific survival (CSS). RESULTS: The overall risk of LNM in patients with T1 colon cancer was 12.0% (N = 967). Adjusted logistic regression models revealed that mucinous carcinoma [odds ratio (OR) = 2.26, P < 0.001], moderately differentiated (OR 1.74, P < 0.001), poorly differentiated (OR 5.16, P < 0.001), and undifferentiated carcinoma (OR 3.01, P = 0.003); older age (OR 0.66, P < 0.001 for age 65–79 years, OR 0.44, P < 0.001 for age over 80 years); and carcinoma located in the ascending colon (OR 0.77, P = 0.018) and sigmoid colon (OR 1.24, P = 0.014) were independent predictive factors for LNM. Adjusted Cox regression analysis showed that positive lymph node involvement was significantly associated with CSS [hazard ratio (HR) = 3.02, P < 0.001], which was further robustly confirmed using a competing risks model and the CIF. CONCLUSIONS: This population-based study showed that mucinous carcinoma, tumor grade, age, and primary tumor location were independent predictive factors for LNM in T1 colon cancer. The risk of LNM should be carefully evaluated in patients with T1 colon cancer, before clinical management. Springer US 2019-10-16 2020 /pmc/articles/PMC7395001/ /pubmed/31620912 http://dx.doi.org/10.1007/s00464-019-07192-0 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Xu, Xin
Zhang, Chihao
Ni, Xiaochun
Wu, Jugang
Pan, Chunpeng
Wang, Shoulian
Yu, Jiwei
Population-based analysis on predictors for lymph node metastasis in T1 colon cancer
title Population-based analysis on predictors for lymph node metastasis in T1 colon cancer
title_full Population-based analysis on predictors for lymph node metastasis in T1 colon cancer
title_fullStr Population-based analysis on predictors for lymph node metastasis in T1 colon cancer
title_full_unstemmed Population-based analysis on predictors for lymph node metastasis in T1 colon cancer
title_short Population-based analysis on predictors for lymph node metastasis in T1 colon cancer
title_sort population-based analysis on predictors for lymph node metastasis in t1 colon cancer
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7395001/
https://www.ncbi.nlm.nih.gov/pubmed/31620912
http://dx.doi.org/10.1007/s00464-019-07192-0
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