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Doubling time of circulating cea and its relation to survival of patients with recurrent colorectal cancer.
In a retrospective study the postoperative time courses of CEA in colorectal cancer patients with recurrent disease were analysed. In 87/114 cases with increasing concentrations of circulating CEA under close follow-up a linear relationship between log CEA and time could be established during diseas...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1982
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2011150/ https://www.ncbi.nlm.nih.gov/pubmed/7171456 |
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author | Staab, H. J. Anderer, F. A. Hornung, A. Stumpf, E. Fischer, R. |
author_facet | Staab, H. J. Anderer, F. A. Hornung, A. Stumpf, E. Fischer, R. |
author_sort | Staab, H. J. |
collection | PubMed |
description | In a retrospective study the postoperative time courses of CEA in colorectal cancer patients with recurrent disease were analysed. In 87/114 cases with increasing concentrations of circulating CEA under close follow-up a linear relationship between log CEA and time could be established during disease recurrence. The individual doubling times of the serum CEA concentration in the log CEA period were calculated and found to cover distinct ranges dependent on the diagnosis of disease recurrence. The CEA doubling times concomitant with local recurrence or second primary carcinomas ranged from 142 to 868 days, visceral metastasis other than liver metastasis from 47 to 231 days and liver metastasis from 10 to 102 days. Patients with bone metastases exhibited CEA doubling times of 54-60 days and a patient with brain metastasis had a CEA doubling time of 598 days. The CEA doubling times of patients with liver metastasis and no further treatment, correlated well with the time of survival after the initial CEA increase of the log CEA phase (r = 0.870, n = 33). The mean survival expressed in multiples of the individual CEA doubling times was 7.0 +/- 1.8. Patients with liver metastasis who underwent various treatments of recurrent disease had a distinctly longer mean survival of 17.4 +/- 9.4 CEA doubling times (P less than 0.001). CEA doubling times can be used as a potential method to assess the efficacy of various treatments. |
format | Text |
id | pubmed-2011150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1982 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20111502009-09-10 Doubling time of circulating cea and its relation to survival of patients with recurrent colorectal cancer. Staab, H. J. Anderer, F. A. Hornung, A. Stumpf, E. Fischer, R. Br J Cancer Research Article In a retrospective study the postoperative time courses of CEA in colorectal cancer patients with recurrent disease were analysed. In 87/114 cases with increasing concentrations of circulating CEA under close follow-up a linear relationship between log CEA and time could be established during disease recurrence. The individual doubling times of the serum CEA concentration in the log CEA period were calculated and found to cover distinct ranges dependent on the diagnosis of disease recurrence. The CEA doubling times concomitant with local recurrence or second primary carcinomas ranged from 142 to 868 days, visceral metastasis other than liver metastasis from 47 to 231 days and liver metastasis from 10 to 102 days. Patients with bone metastases exhibited CEA doubling times of 54-60 days and a patient with brain metastasis had a CEA doubling time of 598 days. The CEA doubling times of patients with liver metastasis and no further treatment, correlated well with the time of survival after the initial CEA increase of the log CEA phase (r = 0.870, n = 33). The mean survival expressed in multiples of the individual CEA doubling times was 7.0 +/- 1.8. Patients with liver metastasis who underwent various treatments of recurrent disease had a distinctly longer mean survival of 17.4 +/- 9.4 CEA doubling times (P less than 0.001). CEA doubling times can be used as a potential method to assess the efficacy of various treatments. Nature Publishing Group 1982-11 /pmc/articles/PMC2011150/ /pubmed/7171456 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 Staab, H. J. Anderer, F. A. Hornung, A. Stumpf, E. Fischer, R. Doubling time of circulating cea and its relation to survival of patients with recurrent colorectal cancer. |
title | Doubling time of circulating cea and its relation to survival of patients with recurrent colorectal cancer. |
title_full | Doubling time of circulating cea and its relation to survival of patients with recurrent colorectal cancer. |
title_fullStr | Doubling time of circulating cea and its relation to survival of patients with recurrent colorectal cancer. |
title_full_unstemmed | Doubling time of circulating cea and its relation to survival of patients with recurrent colorectal cancer. |
title_short | Doubling time of circulating cea and its relation to survival of patients with recurrent colorectal cancer. |
title_sort | doubling time of circulating cea and its relation to survival of patients with recurrent colorectal cancer. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2011150/ https://www.ncbi.nlm.nih.gov/pubmed/7171456 |
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