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Carcinoembryonic antigen level of draining venous blood as a predictor of recurrence in colorectal cancer patient
PURPOSE: We designed this study to evaluate the efficacy of carcinoembryonic antigen in draining venous blood (vCEA) as a predictor of recurrence. METHODS: Draining venous and supplying arterial bloods were collected separately during the operation of 82 colorectal cancer patients without distant me...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Surgical Society
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3243855/ https://www.ncbi.nlm.nih.gov/pubmed/22200039 http://dx.doi.org/10.4174/jkss.2011.81.6.387 |
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author | Lee, Soo Young Min, Kyung Sun Chung, Jung Kee Jung, In Mok Ahn, Young Joon Hwang, Ki-Tae Ahn, Hye Seong Heo, Seung Chul |
author_facet | Lee, Soo Young Min, Kyung Sun Chung, Jung Kee Jung, In Mok Ahn, Young Joon Hwang, Ki-Tae Ahn, Hye Seong Heo, Seung Chul |
author_sort | Lee, Soo Young |
collection | PubMed |
description | PURPOSE: We designed this study to evaluate the efficacy of carcinoembryonic antigen in draining venous blood (vCEA) as a predictor of recurrence. METHODS: Draining venous and supplying arterial bloods were collected separately during the operation of 82 colorectal cancer patients without distant metastasis from September 2004 to December 2006. Carcinoembryonic antigen was measured and assessed for the efficacy as a prognostic factor of recurrence using receiver operating characteristic (ROC) and Kaplan-Meier curves. RESULTS: vCEA is a statistically significant factor that predicts recurrence (P = 0.032) and the optimal cut-off value for vCEA from ROC curve is 8.0 ng/mL. The recurrence-free survival between patients with vCEA levels >8 ng/mL and ≤8 ng/mL significantly differed (P < 0.001). The significance of vCEA as a predictor of recurrence gets higher when limited to patients without lymph node metastasis. The proper cut-off value for vCEA is 4.0 ng/mL if confined to patients without lymph node metastasis. The recurrence-free survival between the patients of vCEA levels >4 ng/mL and ≤4 ng/mL significantly differed (P < 0.001). Multivariate analysis revealed vCEA is an independent prognostic factor in patients without lymph node metastasis. CONCLUSION: vCEA is an independent prognostic factor of recurrence in colorectal cancer patients especially in patients without lymph node metastases. |
format | Online Article Text |
id | pubmed-3243855 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The Korean Surgical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-32438552011-12-23 Carcinoembryonic antigen level of draining venous blood as a predictor of recurrence in colorectal cancer patient Lee, Soo Young Min, Kyung Sun Chung, Jung Kee Jung, In Mok Ahn, Young Joon Hwang, Ki-Tae Ahn, Hye Seong Heo, Seung Chul J Korean Surg Soc Original Article PURPOSE: We designed this study to evaluate the efficacy of carcinoembryonic antigen in draining venous blood (vCEA) as a predictor of recurrence. METHODS: Draining venous and supplying arterial bloods were collected separately during the operation of 82 colorectal cancer patients without distant metastasis from September 2004 to December 2006. Carcinoembryonic antigen was measured and assessed for the efficacy as a prognostic factor of recurrence using receiver operating characteristic (ROC) and Kaplan-Meier curves. RESULTS: vCEA is a statistically significant factor that predicts recurrence (P = 0.032) and the optimal cut-off value for vCEA from ROC curve is 8.0 ng/mL. The recurrence-free survival between patients with vCEA levels >8 ng/mL and ≤8 ng/mL significantly differed (P < 0.001). The significance of vCEA as a predictor of recurrence gets higher when limited to patients without lymph node metastasis. The proper cut-off value for vCEA is 4.0 ng/mL if confined to patients without lymph node metastasis. The recurrence-free survival between the patients of vCEA levels >4 ng/mL and ≤4 ng/mL significantly differed (P < 0.001). Multivariate analysis revealed vCEA is an independent prognostic factor in patients without lymph node metastasis. CONCLUSION: vCEA is an independent prognostic factor of recurrence in colorectal cancer patients especially in patients without lymph node metastases. The Korean Surgical Society 2011-12 2011-11-25 /pmc/articles/PMC3243855/ /pubmed/22200039 http://dx.doi.org/10.4174/jkss.2011.81.6.387 Text en Copyright © 2011, the Korean Surgical Society http://creativecommons.org/licenses/by-nc/3.0 Journal of the Korean Surgical Society 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/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Lee, Soo Young Min, Kyung Sun Chung, Jung Kee Jung, In Mok Ahn, Young Joon Hwang, Ki-Tae Ahn, Hye Seong Heo, Seung Chul Carcinoembryonic antigen level of draining venous blood as a predictor of recurrence in colorectal cancer patient |
title | Carcinoembryonic antigen level of draining venous blood as a predictor of recurrence in colorectal cancer patient |
title_full | Carcinoembryonic antigen level of draining venous blood as a predictor of recurrence in colorectal cancer patient |
title_fullStr | Carcinoembryonic antigen level of draining venous blood as a predictor of recurrence in colorectal cancer patient |
title_full_unstemmed | Carcinoembryonic antigen level of draining venous blood as a predictor of recurrence in colorectal cancer patient |
title_short | Carcinoembryonic antigen level of draining venous blood as a predictor of recurrence in colorectal cancer patient |
title_sort | carcinoembryonic antigen level of draining venous blood as a predictor of recurrence in colorectal cancer patient |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3243855/ https://www.ncbi.nlm.nih.gov/pubmed/22200039 http://dx.doi.org/10.4174/jkss.2011.81.6.387 |
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