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Detection of D2-40 monoclonal antibody-labeled lymphatic vessel invasion in esophageal squamous cell carcinoma and its clinicopathologic significance
OBJECTIVE: This study aims to investigate the clinicopathologic significance of lymphatic vessel invasion (LVI) labeled by D2-40 monoclonal antibody in esophageal squamous cell carcinoma (ESCC). METHODS: Immunohistochemical assay was used to detect the expression of D2-40 and LVI in 107 ESCC patient...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Chinese Anti-Cancer Association
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3719196/ https://www.ncbi.nlm.nih.gov/pubmed/23882422 http://dx.doi.org/10.7497/j.issn.2095-3941.2013.02.003 |
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author | Bai, Bing Ma, Wei Wang, Kai Ha, Sita Wang, Jian-Bo Tan, Bing-Xu Wang, Na-Na Yang, Sheng-Si Jia, Yi-Bin Cheng, Yu-Feng |
author_facet | Bai, Bing Ma, Wei Wang, Kai Ha, Sita Wang, Jian-Bo Tan, Bing-Xu Wang, Na-Na Yang, Sheng-Si Jia, Yi-Bin Cheng, Yu-Feng |
author_sort | Bai, Bing |
collection | PubMed |
description | OBJECTIVE: This study aims to investigate the clinicopathologic significance of lymphatic vessel invasion (LVI) labeled by D2-40 monoclonal antibody in esophageal squamous cell carcinoma (ESCC). METHODS: Immunohistochemical assay was used to detect the expression of D2-40 and LVI in 107 ESCC patients. Then, the correlation between the clinicopathologic feature and the overall survival time of the patients was analyzed. RESULTS: The lymph node metastasis rates were 70% and 21% in the LVI-positive and LVI-negative groups, respectively. The nodal metastasis rate was higher in the LVI-positive group than in the LVI-negative group. Multivariate regression analysis showed that LVI was related to nodal metastasis (P<0.001). The median survival time of the patients was 26 and 43 months in the LVI-positive and LVI-negative groups, respectively. Although univariate regression analysis showed significant difference between the two groups (P=0.014), multivariate regression analysis revealed that LVI was not an independent prognostic factor for overall survival in the ESCC patients (P=0.062). Lymphatic node metastasis (P=0.031), clinical stage (P=0.019), and residual tumor (P=0.026) were the independent prognostic factors. CONCLUSION: LVI labeled by D2-40 monoclonal antibody is a risk factor predictive of lymph node metastasis in ESCC patients. |
format | Online Article Text |
id | pubmed-3719196 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Chinese Anti-Cancer Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-37191962013-07-23 Detection of D2-40 monoclonal antibody-labeled lymphatic vessel invasion in esophageal squamous cell carcinoma and its clinicopathologic significance Bai, Bing Ma, Wei Wang, Kai Ha, Sita Wang, Jian-Bo Tan, Bing-Xu Wang, Na-Na Yang, Sheng-Si Jia, Yi-Bin Cheng, Yu-Feng Cancer Biol Med Original Article OBJECTIVE: This study aims to investigate the clinicopathologic significance of lymphatic vessel invasion (LVI) labeled by D2-40 monoclonal antibody in esophageal squamous cell carcinoma (ESCC). METHODS: Immunohistochemical assay was used to detect the expression of D2-40 and LVI in 107 ESCC patients. Then, the correlation between the clinicopathologic feature and the overall survival time of the patients was analyzed. RESULTS: The lymph node metastasis rates were 70% and 21% in the LVI-positive and LVI-negative groups, respectively. The nodal metastasis rate was higher in the LVI-positive group than in the LVI-negative group. Multivariate regression analysis showed that LVI was related to nodal metastasis (P<0.001). The median survival time of the patients was 26 and 43 months in the LVI-positive and LVI-negative groups, respectively. Although univariate regression analysis showed significant difference between the two groups (P=0.014), multivariate regression analysis revealed that LVI was not an independent prognostic factor for overall survival in the ESCC patients (P=0.062). Lymphatic node metastasis (P=0.031), clinical stage (P=0.019), and residual tumor (P=0.026) were the independent prognostic factors. CONCLUSION: LVI labeled by D2-40 monoclonal antibody is a risk factor predictive of lymph node metastasis in ESCC patients. Chinese Anti-Cancer Association 2013-06 /pmc/articles/PMC3719196/ /pubmed/23882422 http://dx.doi.org/10.7497/j.issn.2095-3941.2013.02.003 Text en 2013 Cancer Biology & Medicine This work is licensed under a Creative Commons Attribution 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Original Article Bai, Bing Ma, Wei Wang, Kai Ha, Sita Wang, Jian-Bo Tan, Bing-Xu Wang, Na-Na Yang, Sheng-Si Jia, Yi-Bin Cheng, Yu-Feng Detection of D2-40 monoclonal antibody-labeled lymphatic vessel invasion in esophageal squamous cell carcinoma and its clinicopathologic significance |
title | Detection of D2-40 monoclonal antibody-labeled lymphatic vessel invasion in esophageal squamous cell carcinoma and its clinicopathologic significance |
title_full | Detection of D2-40 monoclonal antibody-labeled lymphatic vessel invasion in esophageal squamous cell carcinoma and its clinicopathologic significance |
title_fullStr | Detection of D2-40 monoclonal antibody-labeled lymphatic vessel invasion in esophageal squamous cell carcinoma and its clinicopathologic significance |
title_full_unstemmed | Detection of D2-40 monoclonal antibody-labeled lymphatic vessel invasion in esophageal squamous cell carcinoma and its clinicopathologic significance |
title_short | Detection of D2-40 monoclonal antibody-labeled lymphatic vessel invasion in esophageal squamous cell carcinoma and its clinicopathologic significance |
title_sort | detection of d2-40 monoclonal antibody-labeled lymphatic vessel invasion in esophageal squamous cell carcinoma and its clinicopathologic significance |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3719196/ https://www.ncbi.nlm.nih.gov/pubmed/23882422 http://dx.doi.org/10.7497/j.issn.2095-3941.2013.02.003 |
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