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Influence of metastatic site as an additional predictor for response and outcome in advanced colorectal carcinoma

Every year, 31 230 men and women are diagnosed with colorectal carcinoma, and up to 60% of these will ultimately develop advanced disease. However, there is little information to identify which patients are most likely to benefit from palliative chemotherapy. This analysis is unique in evaluating ho...

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Autores principales: Assersohn, L, Norman, A, Cunningham, D, Benepal, T, Ross, P J, Oates, J
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 1999
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362782/
https://www.ncbi.nlm.nih.gov/pubmed/10206296
http://dx.doi.org/10.1038/sj.bjc.6990287
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author Assersohn, L
Norman, A
Cunningham, D
Benepal, T
Ross, P J
Oates, J
author_facet Assersohn, L
Norman, A
Cunningham, D
Benepal, T
Ross, P J
Oates, J
author_sort Assersohn, L
collection PubMed
description Every year, 31 230 men and women are diagnosed with colorectal carcinoma, and up to 60% of these will ultimately develop advanced disease. However, there is little information to identify which patients are most likely to benefit from palliative chemotherapy. This analysis is unique in evaluating how the site of metastasis influences response and survival. A database of 497 patients treated within randomized clinical trials using 5-Fluorouracil (5FU)-based chemotherapy at the Royal Marsden Hospital was analysed. The potential for site of metastasis as a predictive variable for response to chemotherapy and survival was examined, in addition to other clinical parameters. The presence of liver metastases was a better predictor for overall response than either performance status or number of metastatic sites on presentation. Probability of response was significantly decreased by a raised serum carcinoembryonic antigen (CEA) and presence of peritoneal metastases. In liver metastases, a normal serum albumin was as significant a predictor for response as good performance status. The most important predictor for survival was initial performance status. The number of metastatic sites on presentation had no influence on survival. Site of metastasis can predict for response to 5FU-based chemotherapy and patients should be stratified according to the involved site of metastasis in the future. © 1999 Cancer Research Campaign
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spelling pubmed-23627822009-09-10 Influence of metastatic site as an additional predictor for response and outcome in advanced colorectal carcinoma Assersohn, L Norman, A Cunningham, D Benepal, T Ross, P J Oates, J Br J Cancer Regular Article Every year, 31 230 men and women are diagnosed with colorectal carcinoma, and up to 60% of these will ultimately develop advanced disease. However, there is little information to identify which patients are most likely to benefit from palliative chemotherapy. This analysis is unique in evaluating how the site of metastasis influences response and survival. A database of 497 patients treated within randomized clinical trials using 5-Fluorouracil (5FU)-based chemotherapy at the Royal Marsden Hospital was analysed. The potential for site of metastasis as a predictive variable for response to chemotherapy and survival was examined, in addition to other clinical parameters. The presence of liver metastases was a better predictor for overall response than either performance status or number of metastatic sites on presentation. Probability of response was significantly decreased by a raised serum carcinoembryonic antigen (CEA) and presence of peritoneal metastases. In liver metastases, a normal serum albumin was as significant a predictor for response as good performance status. The most important predictor for survival was initial performance status. The number of metastatic sites on presentation had no influence on survival. Site of metastasis can predict for response to 5FU-based chemotherapy and patients should be stratified according to the involved site of metastasis in the future. © 1999 Cancer Research Campaign Nature Publishing Group 1999-04 /pmc/articles/PMC2362782/ /pubmed/10206296 http://dx.doi.org/10.1038/sj.bjc.6990287 Text en Copyright © 1999 Cancer Research Campaign 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 Regular Article
Assersohn, L
Norman, A
Cunningham, D
Benepal, T
Ross, P J
Oates, J
Influence of metastatic site as an additional predictor for response and outcome in advanced colorectal carcinoma
title Influence of metastatic site as an additional predictor for response and outcome in advanced colorectal carcinoma
title_full Influence of metastatic site as an additional predictor for response and outcome in advanced colorectal carcinoma
title_fullStr Influence of metastatic site as an additional predictor for response and outcome in advanced colorectal carcinoma
title_full_unstemmed Influence of metastatic site as an additional predictor for response and outcome in advanced colorectal carcinoma
title_short Influence of metastatic site as an additional predictor for response and outcome in advanced colorectal carcinoma
title_sort influence of metastatic site as an additional predictor for response and outcome in advanced colorectal carcinoma
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362782/
https://www.ncbi.nlm.nih.gov/pubmed/10206296
http://dx.doi.org/10.1038/sj.bjc.6990287
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