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The role of CA-242 and CEA in surveillance following curative resection for colorectal cancer.
This study was undertaken to evaluate the role of a new tumour marker, CA-242, alone or in combination with CEA in the practical management of colorectal cancer patients after potentially curative resection. A cohort of 149 patients who had undergone 'curative' surgery was followed up acco...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1994
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033359/ https://www.ncbi.nlm.nih.gov/pubmed/8080745 |
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author | Hall, N. R. Finan, P. J. Stephenson, B. M. Purves, D. A. Cooper, E. H. |
author_facet | Hall, N. R. Finan, P. J. Stephenson, B. M. Purves, D. A. Cooper, E. H. |
author_sort | Hall, N. R. |
collection | PubMed |
description | This study was undertaken to evaluate the role of a new tumour marker, CA-242, alone or in combination with CEA in the practical management of colorectal cancer patients after potentially curative resection. A cohort of 149 patients who had undergone 'curative' surgery was followed up according to an intensive protocol in order to detect recurrent disease. Over a median tumour marker follow-up period of 24 months there were 25 recurrences in 24 patients. Both CEA and CA-242 alone detected half the local recurrences. The sensitivity of CEA was 84% for distant or mixed recurrence compared with 64% for CA-242. An abnormality of either CEA or CA-242 enabled detection of five out of six local recurrences and 17 out of 19 distant or mixed recurrences with a median lead time of 5 months for each marker. Both markers were elevated concurrently in only one local and 11 distant recurrences. While CA-242 alone is not superior to CEA, their combined use (either abnormal) has a high sensitivity (88%), specificity (78%) and negative predictive value (97%); this may be useful in reducing unnecessary investigations in follow-up programmes and as a guide to the initiation of further treatment for recurrent disease. |
format | Text |
id | pubmed-2033359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1994 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20333592009-09-10 The role of CA-242 and CEA in surveillance following curative resection for colorectal cancer. Hall, N. R. Finan, P. J. Stephenson, B. M. Purves, D. A. Cooper, E. H. Br J Cancer Research Article This study was undertaken to evaluate the role of a new tumour marker, CA-242, alone or in combination with CEA in the practical management of colorectal cancer patients after potentially curative resection. A cohort of 149 patients who had undergone 'curative' surgery was followed up according to an intensive protocol in order to detect recurrent disease. Over a median tumour marker follow-up period of 24 months there were 25 recurrences in 24 patients. Both CEA and CA-242 alone detected half the local recurrences. The sensitivity of CEA was 84% for distant or mixed recurrence compared with 64% for CA-242. An abnormality of either CEA or CA-242 enabled detection of five out of six local recurrences and 17 out of 19 distant or mixed recurrences with a median lead time of 5 months for each marker. Both markers were elevated concurrently in only one local and 11 distant recurrences. While CA-242 alone is not superior to CEA, their combined use (either abnormal) has a high sensitivity (88%), specificity (78%) and negative predictive value (97%); this may be useful in reducing unnecessary investigations in follow-up programmes and as a guide to the initiation of further treatment for recurrent disease. Nature Publishing Group 1994-09 /pmc/articles/PMC2033359/ /pubmed/8080745 Text en 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 | Research Article Hall, N. R. Finan, P. J. Stephenson, B. M. Purves, D. A. Cooper, E. H. The role of CA-242 and CEA in surveillance following curative resection for colorectal cancer. |
title | The role of CA-242 and CEA in surveillance following curative resection for colorectal cancer. |
title_full | The role of CA-242 and CEA in surveillance following curative resection for colorectal cancer. |
title_fullStr | The role of CA-242 and CEA in surveillance following curative resection for colorectal cancer. |
title_full_unstemmed | The role of CA-242 and CEA in surveillance following curative resection for colorectal cancer. |
title_short | The role of CA-242 and CEA in surveillance following curative resection for colorectal cancer. |
title_sort | role of ca-242 and cea in surveillance following curative resection for colorectal cancer. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2033359/ https://www.ncbi.nlm.nih.gov/pubmed/8080745 |
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