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Histopathologic risk factors for lymph node metastasis in patients with T1 colorectal cancer

PURPOSE: Evaluating the risk of lymph node metastasis (LNM) is critical for determining subsequent treatments following endoscopic resection of T1 colorectal cancer (CRC). This study analyzed histopathologic risk factors for LNM in patients with T1 CRC. METHODS: This study involved 745 patients with...

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Autores principales: Ha, Ryun Kyong, Han, Kyung Su, Sohn, Dae Kyung, Kim, Byung Chang, Hong, Chang Won, Chang, Hee Jin, Hyun, Jong Hee, Kim, Min Jung, Park, Sung Chan, Oh, Jae Hwan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Surgical Society 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5694718/
https://www.ncbi.nlm.nih.gov/pubmed/29184880
http://dx.doi.org/10.4174/astr.2017.93.5.266
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author Ha, Ryun Kyong
Han, Kyung Su
Sohn, Dae Kyung
Kim, Byung Chang
Hong, Chang Won
Chang, Hee Jin
Hyun, Jong Hee
Kim, Min Jung
Park, Sung Chan
Oh, Jae Hwan
author_facet Ha, Ryun Kyong
Han, Kyung Su
Sohn, Dae Kyung
Kim, Byung Chang
Hong, Chang Won
Chang, Hee Jin
Hyun, Jong Hee
Kim, Min Jung
Park, Sung Chan
Oh, Jae Hwan
author_sort Ha, Ryun Kyong
collection PubMed
description PURPOSE: Evaluating the risk of lymph node metastasis (LNM) is critical for determining subsequent treatments following endoscopic resection of T1 colorectal cancer (CRC). This study analyzed histopathologic risk factors for LNM in patients with T1 CRC. METHODS: This study involved 745 patients with T1 CRC who underwent endoscopic (n = 97) or surgical (n = 648) resection between January 2001 and December 2015 at the National Cancer Center, Korea. LNM in endoscopically resected patients, which could not be evaluated directly, was estimated indirectly based on follow-up results and histopathologic reports of salvage surgery. The relationships of depth of submucosal invasion, histologic grade, budding, vascular invasion, and background adenoma with LNM were evaluated statistically. RESULTS: Of the 745 patients, 91 (12.2%) were found to be positive for LNM. Univariate and multivariate analyses identified deep submucosal invasion (P = 0.010), histologic high grade (P < 0.001), budding (P = 0.034), and vascular invasion (P < 0.001) as risk factors for LNM. Among the patients with one, two, three, and four risk factors, 6.0%, 18.7%, 36.4%, and 100%, respectively, were positive for LNM. CONCLUSION: Deep submucosal invasion, histologic high grade, budding, and vascular invasion are risk factors for LNM in patients with T1 colorectal cancer. If any of these risk factors are present, additional surgery following endoscopic resection should be determined after considering the potential risk of LNM and each patient's situation.
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spelling pubmed-56947182017-11-28 Histopathologic risk factors for lymph node metastasis in patients with T1 colorectal cancer Ha, Ryun Kyong Han, Kyung Su Sohn, Dae Kyung Kim, Byung Chang Hong, Chang Won Chang, Hee Jin Hyun, Jong Hee Kim, Min Jung Park, Sung Chan Oh, Jae Hwan Ann Surg Treat Res Original Article PURPOSE: Evaluating the risk of lymph node metastasis (LNM) is critical for determining subsequent treatments following endoscopic resection of T1 colorectal cancer (CRC). This study analyzed histopathologic risk factors for LNM in patients with T1 CRC. METHODS: This study involved 745 patients with T1 CRC who underwent endoscopic (n = 97) or surgical (n = 648) resection between January 2001 and December 2015 at the National Cancer Center, Korea. LNM in endoscopically resected patients, which could not be evaluated directly, was estimated indirectly based on follow-up results and histopathologic reports of salvage surgery. The relationships of depth of submucosal invasion, histologic grade, budding, vascular invasion, and background adenoma with LNM were evaluated statistically. RESULTS: Of the 745 patients, 91 (12.2%) were found to be positive for LNM. Univariate and multivariate analyses identified deep submucosal invasion (P = 0.010), histologic high grade (P < 0.001), budding (P = 0.034), and vascular invasion (P < 0.001) as risk factors for LNM. Among the patients with one, two, three, and four risk factors, 6.0%, 18.7%, 36.4%, and 100%, respectively, were positive for LNM. CONCLUSION: Deep submucosal invasion, histologic high grade, budding, and vascular invasion are risk factors for LNM in patients with T1 colorectal cancer. If any of these risk factors are present, additional surgery following endoscopic resection should be determined after considering the potential risk of LNM and each patient's situation. The Korean Surgical Society 2017-11 2017-10-27 /pmc/articles/PMC5694718/ /pubmed/29184880 http://dx.doi.org/10.4174/astr.2017.93.5.266 Text en Copyright © 2017, the Korean Surgical Society http://creativecommons.org/licenses/by-nc/4.0/ Annals of Surgical Treatment and Research is an Open Access Journal. All articles are distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ha, Ryun Kyong
Han, Kyung Su
Sohn, Dae Kyung
Kim, Byung Chang
Hong, Chang Won
Chang, Hee Jin
Hyun, Jong Hee
Kim, Min Jung
Park, Sung Chan
Oh, Jae Hwan
Histopathologic risk factors for lymph node metastasis in patients with T1 colorectal cancer
title Histopathologic risk factors for lymph node metastasis in patients with T1 colorectal cancer
title_full Histopathologic risk factors for lymph node metastasis in patients with T1 colorectal cancer
title_fullStr Histopathologic risk factors for lymph node metastasis in patients with T1 colorectal cancer
title_full_unstemmed Histopathologic risk factors for lymph node metastasis in patients with T1 colorectal cancer
title_short Histopathologic risk factors for lymph node metastasis in patients with T1 colorectal cancer
title_sort histopathologic risk factors for lymph node metastasis in patients with t1 colorectal cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5694718/
https://www.ncbi.nlm.nih.gov/pubmed/29184880
http://dx.doi.org/10.4174/astr.2017.93.5.266
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