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Prospective validation of quantitative CEA mRNA detection in peritoneal washes in gastric carcinoma patients
Prediction of peritoneal relapse is extremely important for gastric cancer patients after curative surgery. The present study prospectively validates the prognostic ability of quantifying carcinoembryonic antigen (CEA) mRNA in peritoneal washes by real-time reverse transcriptase–polymerase chain rea...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361668/ https://www.ncbi.nlm.nih.gov/pubmed/16205696 http://dx.doi.org/10.1038/sj.bjc.6602802 |
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author | Ito, S Nakanishi, H Kodera, Y Mochizuki, Y Tatematsu, M Yamamura, Y |
author_facet | Ito, S Nakanishi, H Kodera, Y Mochizuki, Y Tatematsu, M Yamamura, Y |
author_sort | Ito, S |
collection | PubMed |
description | Prediction of peritoneal relapse is extremely important for gastric cancer patients after curative surgery. The present study prospectively validates the prognostic ability of quantifying carcinoembryonic antigen (CEA) mRNA in peritoneal washes by real-time reverse transcriptase–polymerase chain reaction. Based on a retrospective study of 197 curatively resected gastric cancer patients (training set), we determined a cutoff value of CEA mRNA using receiver-operating characteristic curve. We used this cutoff value to validate the risk of peritoneal recurrence in a new cohort of 86 gastric cancer patients (validation set) between July 2000 and December 2002 in a prospective study. During the median 30 months of postoperative surveillance, 20 of the 86 patients died, and 13 of the 20 developed peritoneal metastases. Peritoneal recurrence-free survival as well as overall survival was significantly worse in patients with positive CEA mRNA (P<0.0001). Multivariate analysis with the Cox proportional hazards model showed that positive CEA mRNA was a significant independent risk factor with both survival (P=0.0130) and peritoneal recurrence-free survival (P=0.0006) as end points. These results indicate that quantitation of CEA mRNA in peritoneal washes is a reliable prognostic indicator of peritoneal recurrence in the clinical setting. |
format | Text |
id | pubmed-2361668 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23616682009-09-10 Prospective validation of quantitative CEA mRNA detection in peritoneal washes in gastric carcinoma patients Ito, S Nakanishi, H Kodera, Y Mochizuki, Y Tatematsu, M Yamamura, Y Br J Cancer Clinical Study Prediction of peritoneal relapse is extremely important for gastric cancer patients after curative surgery. The present study prospectively validates the prognostic ability of quantifying carcinoembryonic antigen (CEA) mRNA in peritoneal washes by real-time reverse transcriptase–polymerase chain reaction. Based on a retrospective study of 197 curatively resected gastric cancer patients (training set), we determined a cutoff value of CEA mRNA using receiver-operating characteristic curve. We used this cutoff value to validate the risk of peritoneal recurrence in a new cohort of 86 gastric cancer patients (validation set) between July 2000 and December 2002 in a prospective study. During the median 30 months of postoperative surveillance, 20 of the 86 patients died, and 13 of the 20 developed peritoneal metastases. Peritoneal recurrence-free survival as well as overall survival was significantly worse in patients with positive CEA mRNA (P<0.0001). Multivariate analysis with the Cox proportional hazards model showed that positive CEA mRNA was a significant independent risk factor with both survival (P=0.0130) and peritoneal recurrence-free survival (P=0.0006) as end points. These results indicate that quantitation of CEA mRNA in peritoneal washes is a reliable prognostic indicator of peritoneal recurrence in the clinical setting. Nature Publishing Group 2005-10-31 2005-10-04 /pmc/articles/PMC2361668/ /pubmed/16205696 http://dx.doi.org/10.1038/sj.bjc.6602802 Text en Copyright © 2005 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Clinical Study Ito, S Nakanishi, H Kodera, Y Mochizuki, Y Tatematsu, M Yamamura, Y Prospective validation of quantitative CEA mRNA detection in peritoneal washes in gastric carcinoma patients |
title | Prospective validation of quantitative CEA mRNA detection in peritoneal washes in gastric carcinoma patients |
title_full | Prospective validation of quantitative CEA mRNA detection in peritoneal washes in gastric carcinoma patients |
title_fullStr | Prospective validation of quantitative CEA mRNA detection in peritoneal washes in gastric carcinoma patients |
title_full_unstemmed | Prospective validation of quantitative CEA mRNA detection in peritoneal washes in gastric carcinoma patients |
title_short | Prospective validation of quantitative CEA mRNA detection in peritoneal washes in gastric carcinoma patients |
title_sort | prospective validation of quantitative cea mrna detection in peritoneal washes in gastric carcinoma patients |
topic | Clinical Study |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361668/ https://www.ncbi.nlm.nih.gov/pubmed/16205696 http://dx.doi.org/10.1038/sj.bjc.6602802 |
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