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Role of biological markers in the clinical outcome of colon cancer
We investigated a number of biological markers, evaluated under strict intralaboratory quality control conditions, in terms of their role in predicting clinical outcome of patients with colon cancer treated with 5-FU-containing regimens. Colon cancer tissue from 263 patients enrolled onto two random...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2002
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376168/ https://www.ncbi.nlm.nih.gov/pubmed/12373601 http://dx.doi.org/10.1038/sj.bjc.6600569 |
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author | Nanni, O Volpi, A Frassineti, G L De Paola, F Granato, A M Dubini, A Zoli, W Scarpi, E Turci, D Oliverio, G Gambi, A Amadori, D |
author_facet | Nanni, O Volpi, A Frassineti, G L De Paola, F Granato, A M Dubini, A Zoli, W Scarpi, E Turci, D Oliverio, G Gambi, A Amadori, D |
author_sort | Nanni, O |
collection | PubMed |
description | We investigated a number of biological markers, evaluated under strict intralaboratory quality control conditions, in terms of their role in predicting clinical outcome of patients with colon cancer treated with 5-FU-containing regimens. Colon cancer tissue from 263 patients enrolled onto two randomised clinical trials were studied for their cytofluorimetrically determined DNA content and their immunohistochemically evaluated microvessel density, vascular endothelial growth factor expression, thymidylate synthase expression and tumour lymphocyte infiltration. Disease-free survival and overall survival of patients were analysed as a function of the different variables. At a median follow up of 57 months, age, gender and Dukes' stage showed an impact on disease-free survival, whereas no biological marker emerged as an indicator of better or worse disease-free survival. Only histological grade and Dukes' stage were found to influence overall survival. The different biological variables, studied with particular attention for determination reliability, proved to have no impact on the clinical outcome of patients with colon cancer. Therefore, other markers must be identified to complement clinico-pathological variables in the management of this disease. British Journal of Cancer (2002) 87, 868–875. doi:10.1038/sj.bjc.6600569 www.bjcancer.com © 2002 Cancer Research UK |
format | Text |
id | pubmed-2376168 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2002 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23761682009-09-10 Role of biological markers in the clinical outcome of colon cancer Nanni, O Volpi, A Frassineti, G L De Paola, F Granato, A M Dubini, A Zoli, W Scarpi, E Turci, D Oliverio, G Gambi, A Amadori, D Br J Cancer Molecular and Cellular Pathology We investigated a number of biological markers, evaluated under strict intralaboratory quality control conditions, in terms of their role in predicting clinical outcome of patients with colon cancer treated with 5-FU-containing regimens. Colon cancer tissue from 263 patients enrolled onto two randomised clinical trials were studied for their cytofluorimetrically determined DNA content and their immunohistochemically evaluated microvessel density, vascular endothelial growth factor expression, thymidylate synthase expression and tumour lymphocyte infiltration. Disease-free survival and overall survival of patients were analysed as a function of the different variables. At a median follow up of 57 months, age, gender and Dukes' stage showed an impact on disease-free survival, whereas no biological marker emerged as an indicator of better or worse disease-free survival. Only histological grade and Dukes' stage were found to influence overall survival. The different biological variables, studied with particular attention for determination reliability, proved to have no impact on the clinical outcome of patients with colon cancer. Therefore, other markers must be identified to complement clinico-pathological variables in the management of this disease. British Journal of Cancer (2002) 87, 868–875. doi:10.1038/sj.bjc.6600569 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-10-07 2002-10-07 /pmc/articles/PMC2376168/ /pubmed/12373601 http://dx.doi.org/10.1038/sj.bjc.6600569 Text en Copyright © 2002 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 | Molecular and Cellular Pathology Nanni, O Volpi, A Frassineti, G L De Paola, F Granato, A M Dubini, A Zoli, W Scarpi, E Turci, D Oliverio, G Gambi, A Amadori, D Role of biological markers in the clinical outcome of colon cancer |
title | Role of biological markers in the clinical outcome of colon cancer |
title_full | Role of biological markers in the clinical outcome of colon cancer |
title_fullStr | Role of biological markers in the clinical outcome of colon cancer |
title_full_unstemmed | Role of biological markers in the clinical outcome of colon cancer |
title_short | Role of biological markers in the clinical outcome of colon cancer |
title_sort | role of biological markers in the clinical outcome of colon cancer |
topic | Molecular and Cellular Pathology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376168/ https://www.ncbi.nlm.nih.gov/pubmed/12373601 http://dx.doi.org/10.1038/sj.bjc.6600569 |
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