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Whether regional lymph nodes evaluation should be equally required for both right and left colon cancer
Despite the adequacy of nodal evaluation was gradually improved for colon cancer, the disparity in nodal examination for right colon cancer (RCC) and left colon cancer (LCC) still begs the question of whether 12 nodes is an appropriate threshold for both RCC and LCC. From Surveillance, Epidemiology,...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312360/ https://www.ncbi.nlm.nih.gov/pubmed/27494866 http://dx.doi.org/10.18632/oncotarget.11007 |
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author | Guan, Xu Chen, Wei Liu, Zheng Jiang, Zheng Hu, Hanqing Zhao, Zhixun Wang, Song Chen, Yinggang Wang, Guiyu Wang, Xishan |
author_facet | Guan, Xu Chen, Wei Liu, Zheng Jiang, Zheng Hu, Hanqing Zhao, Zhixun Wang, Song Chen, Yinggang Wang, Guiyu Wang, Xishan |
author_sort | Guan, Xu |
collection | PubMed |
description | Despite the adequacy of nodal evaluation was gradually improved for colon cancer, the disparity in nodal examination for right colon cancer (RCC) and left colon cancer (LCC) still begs the question of whether 12 nodes is an appropriate threshold for both RCC and LCC. From Surveillance, Epidemiology, and End-Results (SEER) database, we identified 53897 RCC patients and 11822 LCC patients. Compared with LCC patients, RCC patients examined more lymph nodes (18.7 vs 16.3), and more likely to examine ≥12 nodes (P<0.001), whereas RCC patients showed lower rates of node positivity (P<0.001). To balance the nodal disparity between RCC and LCC, we revised the 12-node measure based on different tumor locations. With the X-tile, we determined 15 as the optimal node number for RCC and 11 for LCC. To validate the availability of this revised nodal evaluation, the 5-year cancer specific survival (CSS) was calculated according to the optimal node number in RCC and LCC patients, Cox's regression model were used to further assess the prognostic value of this revised nodal evaluation. The results showed that 5-year CSSs were significantly improved for RCC patients with ≥15 lymph nodes, and also for LCC patients with ≥11 lymph nodes (P<0.001). This revised nodal evaluation could also improve the rate of nodal positivity and long-term survival in both RCC and LCC patients compared with 12-node measure. Therefore, the lymph node examination should be discriminately evaluated for RCC and LCC, instead of using 12-node measure to colon cancer as a whole. |
format | Online Article Text |
id | pubmed-5312360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53123602017-03-06 Whether regional lymph nodes evaluation should be equally required for both right and left colon cancer Guan, Xu Chen, Wei Liu, Zheng Jiang, Zheng Hu, Hanqing Zhao, Zhixun Wang, Song Chen, Yinggang Wang, Guiyu Wang, Xishan Oncotarget Research Paper Despite the adequacy of nodal evaluation was gradually improved for colon cancer, the disparity in nodal examination for right colon cancer (RCC) and left colon cancer (LCC) still begs the question of whether 12 nodes is an appropriate threshold for both RCC and LCC. From Surveillance, Epidemiology, and End-Results (SEER) database, we identified 53897 RCC patients and 11822 LCC patients. Compared with LCC patients, RCC patients examined more lymph nodes (18.7 vs 16.3), and more likely to examine ≥12 nodes (P<0.001), whereas RCC patients showed lower rates of node positivity (P<0.001). To balance the nodal disparity between RCC and LCC, we revised the 12-node measure based on different tumor locations. With the X-tile, we determined 15 as the optimal node number for RCC and 11 for LCC. To validate the availability of this revised nodal evaluation, the 5-year cancer specific survival (CSS) was calculated according to the optimal node number in RCC and LCC patients, Cox's regression model were used to further assess the prognostic value of this revised nodal evaluation. The results showed that 5-year CSSs were significantly improved for RCC patients with ≥15 lymph nodes, and also for LCC patients with ≥11 lymph nodes (P<0.001). This revised nodal evaluation could also improve the rate of nodal positivity and long-term survival in both RCC and LCC patients compared with 12-node measure. Therefore, the lymph node examination should be discriminately evaluated for RCC and LCC, instead of using 12-node measure to colon cancer as a whole. Impact Journals LLC 2016-08-02 /pmc/articles/PMC5312360/ /pubmed/27494866 http://dx.doi.org/10.18632/oncotarget.11007 Text en Copyright: © 2016 Guan et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Guan, Xu Chen, Wei Liu, Zheng Jiang, Zheng Hu, Hanqing Zhao, Zhixun Wang, Song Chen, Yinggang Wang, Guiyu Wang, Xishan Whether regional lymph nodes evaluation should be equally required for both right and left colon cancer |
title | Whether regional lymph nodes evaluation should be equally required for both right and left colon cancer |
title_full | Whether regional lymph nodes evaluation should be equally required for both right and left colon cancer |
title_fullStr | Whether regional lymph nodes evaluation should be equally required for both right and left colon cancer |
title_full_unstemmed | Whether regional lymph nodes evaluation should be equally required for both right and left colon cancer |
title_short | Whether regional lymph nodes evaluation should be equally required for both right and left colon cancer |
title_sort | whether regional lymph nodes evaluation should be equally required for both right and left colon cancer |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312360/ https://www.ncbi.nlm.nih.gov/pubmed/27494866 http://dx.doi.org/10.18632/oncotarget.11007 |
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