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Clinicopathological Characteristics of Alpha-Fetoprotein-Producing Gastric Cancer
PURPOSE: α-fetoprotein (AFP)-producing gastric cancer is a rare tumor with high rates of liver metastasis and a poor prognosis. Many studies have been performed but there have been no comprehensive investigations of the clinicopathological and prognosis. MATERIALS AND METHODS: Six hundred ninety fou...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Gastric Cancer Association
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3204474/ https://www.ncbi.nlm.nih.gov/pubmed/22076198 http://dx.doi.org/10.5230/jgc.2011.11.1.23 |
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author | Chun, Huan Kwon, Sung Joon |
author_facet | Chun, Huan Kwon, Sung Joon |
author_sort | Chun, Huan |
collection | PubMed |
description | PURPOSE: α-fetoprotein (AFP)-producing gastric cancer is a rare tumor with high rates of liver metastasis and a poor prognosis. Many studies have been performed but there have been no comprehensive investigations of the clinicopathological and prognosis. MATERIALS AND METHODS: Six hundred ninety four patients with gastric cancer who underwent a curative gastric resection in Hanyang University Hospital from February 2001 to December 2008 were evaluated retrospectively after excluding active or chronic hepatits, liver cirrhosis and preoperative distant metastasis. Among them, thirty five patients had an elevated serum level of AFP (>7 ng/ml) preoperatively. The clinicopathological features of AFP-producing gastric cancer were analyzed. RESULTS: There was poorer differentiation, a higher incidence of lymph node metastasis, more marked lymphatic and vascular invasion in the AFP-positive group than in the AFP-negative group. The 5-year survival rate of the AFP-positive group was significantly poorer than that in the AFP-negative group (66% vs. 80%, P=0.002). A significantly higher incidence of liver metastasis was observed in the AFP-positive group than in the AFP-negative group (14.3% vs. 3.6%, P=0.002) with a shorter median time period from the operation to the metachronous liver metastasis (3.7 months vs. 14.1 months, P=0.043). Multivariate survival analysis revealed the depth of invasion, degree of lymph node metastasis and AFP-positivity to be the independent prognostic factors. CONCLUSIONS: AFP-producing gastric cancers have an aggressive behavior with a high metastatic potential to the liver. In addition, their clinicopathological features are quite different from the more common AFP-negative gastric cancer. |
format | Online Article Text |
id | pubmed-3204474 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The Korean Gastric Cancer Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-32044742011-11-10 Clinicopathological Characteristics of Alpha-Fetoprotein-Producing Gastric Cancer Chun, Huan Kwon, Sung Joon J Gastric Cancer Original Article PURPOSE: α-fetoprotein (AFP)-producing gastric cancer is a rare tumor with high rates of liver metastasis and a poor prognosis. Many studies have been performed but there have been no comprehensive investigations of the clinicopathological and prognosis. MATERIALS AND METHODS: Six hundred ninety four patients with gastric cancer who underwent a curative gastric resection in Hanyang University Hospital from February 2001 to December 2008 were evaluated retrospectively after excluding active or chronic hepatits, liver cirrhosis and preoperative distant metastasis. Among them, thirty five patients had an elevated serum level of AFP (>7 ng/ml) preoperatively. The clinicopathological features of AFP-producing gastric cancer were analyzed. RESULTS: There was poorer differentiation, a higher incidence of lymph node metastasis, more marked lymphatic and vascular invasion in the AFP-positive group than in the AFP-negative group. The 5-year survival rate of the AFP-positive group was significantly poorer than that in the AFP-negative group (66% vs. 80%, P=0.002). A significantly higher incidence of liver metastasis was observed in the AFP-positive group than in the AFP-negative group (14.3% vs. 3.6%, P=0.002) with a shorter median time period from the operation to the metachronous liver metastasis (3.7 months vs. 14.1 months, P=0.043). Multivariate survival analysis revealed the depth of invasion, degree of lymph node metastasis and AFP-positivity to be the independent prognostic factors. CONCLUSIONS: AFP-producing gastric cancers have an aggressive behavior with a high metastatic potential to the liver. In addition, their clinicopathological features are quite different from the more common AFP-negative gastric cancer. The Korean Gastric Cancer Association 2011-03 2011-03-31 /pmc/articles/PMC3204474/ /pubmed/22076198 http://dx.doi.org/10.5230/jgc.2011.11.1.23 Text en Copyright © 2011 by The Korean Gastric Cancer Association http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Chun, Huan Kwon, Sung Joon Clinicopathological Characteristics of Alpha-Fetoprotein-Producing Gastric Cancer |
title | Clinicopathological Characteristics of Alpha-Fetoprotein-Producing Gastric Cancer |
title_full | Clinicopathological Characteristics of Alpha-Fetoprotein-Producing Gastric Cancer |
title_fullStr | Clinicopathological Characteristics of Alpha-Fetoprotein-Producing Gastric Cancer |
title_full_unstemmed | Clinicopathological Characteristics of Alpha-Fetoprotein-Producing Gastric Cancer |
title_short | Clinicopathological Characteristics of Alpha-Fetoprotein-Producing Gastric Cancer |
title_sort | clinicopathological characteristics of alpha-fetoprotein-producing gastric cancer |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3204474/ https://www.ncbi.nlm.nih.gov/pubmed/22076198 http://dx.doi.org/10.5230/jgc.2011.11.1.23 |
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