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Disseminated tumour cells as a prognostic biomarker in colorectal cancer
BACKGROUND: The study was performed to determine detection rate and prognostic relevance of disseminated tumour cells (DTC) in patients receiving curatively intended surgery for colorectal cancer (CRC). METHODS: The study population consisted of 235 patients with CRC prospectively recruited from fiv...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101945/ https://www.ncbi.nlm.nih.gov/pubmed/21448171 http://dx.doi.org/10.1038/bjc.2011.97 |
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author | Flatmark, K Borgen, E Nesland, J M Rasmussen, H Johannessen, H-O Bukholm, I Rosales, R Hårklau, L Jacobsen, H J Sandstad, B Boye, K Fodstad, Ø |
author_facet | Flatmark, K Borgen, E Nesland, J M Rasmussen, H Johannessen, H-O Bukholm, I Rosales, R Hårklau, L Jacobsen, H J Sandstad, B Boye, K Fodstad, Ø |
author_sort | Flatmark, K |
collection | PubMed |
description | BACKGROUND: The study was performed to determine detection rate and prognostic relevance of disseminated tumour cells (DTC) in patients receiving curatively intended surgery for colorectal cancer (CRC). METHODS: The study population consisted of 235 patients with CRC prospectively recruited from five hospitals in the Oslo region. Bone marrow (BM) aspirates were collected at the time of surgery and the presence of DTC was determined by two immunological methods; immunomagnetic selection (using an anti-EpCAM antibody) and immunocytochemistry (using a pan-cytokeratin antibody). Associations between the presence of DTC and metastasis-free, disease-specific and overall survival were analysed using univariate and multivariate methods. RESULTS: Disseminated tumour cells were detected in 41 (17%) and 28 (12%) of the 235 examined BM samples by immunomagnetic selection and immunocytochemistry, respectively, with only five samples being positive with both methods. The presence of DTC was associated with adverse outcome (metastasis-free, disease-specific and overall survival) in univariate and multivariate analyses. CONCLUSION: The presence of DTC was associated with adverse prognosis in this cohort of patients curatively resected for CRC, suggesting that DTC detection still holds promise as a biomarker in CRC. |
format | Text |
id | pubmed-3101945 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-31019452012-04-26 Disseminated tumour cells as a prognostic biomarker in colorectal cancer Flatmark, K Borgen, E Nesland, J M Rasmussen, H Johannessen, H-O Bukholm, I Rosales, R Hårklau, L Jacobsen, H J Sandstad, B Boye, K Fodstad, Ø Br J Cancer Molecular Diagnostics BACKGROUND: The study was performed to determine detection rate and prognostic relevance of disseminated tumour cells (DTC) in patients receiving curatively intended surgery for colorectal cancer (CRC). METHODS: The study population consisted of 235 patients with CRC prospectively recruited from five hospitals in the Oslo region. Bone marrow (BM) aspirates were collected at the time of surgery and the presence of DTC was determined by two immunological methods; immunomagnetic selection (using an anti-EpCAM antibody) and immunocytochemistry (using a pan-cytokeratin antibody). Associations between the presence of DTC and metastasis-free, disease-specific and overall survival were analysed using univariate and multivariate methods. RESULTS: Disseminated tumour cells were detected in 41 (17%) and 28 (12%) of the 235 examined BM samples by immunomagnetic selection and immunocytochemistry, respectively, with only five samples being positive with both methods. The presence of DTC was associated with adverse outcome (metastasis-free, disease-specific and overall survival) in univariate and multivariate analyses. CONCLUSION: The presence of DTC was associated with adverse prognosis in this cohort of patients curatively resected for CRC, suggesting that DTC detection still holds promise as a biomarker in CRC. Nature Publishing Group 2011-04-26 2011-03-29 /pmc/articles/PMC3101945/ /pubmed/21448171 http://dx.doi.org/10.1038/bjc.2011.97 Text en Copyright © 2011 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 Diagnostics Flatmark, K Borgen, E Nesland, J M Rasmussen, H Johannessen, H-O Bukholm, I Rosales, R Hårklau, L Jacobsen, H J Sandstad, B Boye, K Fodstad, Ø Disseminated tumour cells as a prognostic biomarker in colorectal cancer |
title | Disseminated tumour cells as a prognostic biomarker in colorectal cancer |
title_full | Disseminated tumour cells as a prognostic biomarker in colorectal cancer |
title_fullStr | Disseminated tumour cells as a prognostic biomarker in colorectal cancer |
title_full_unstemmed | Disseminated tumour cells as a prognostic biomarker in colorectal cancer |
title_short | Disseminated tumour cells as a prognostic biomarker in colorectal cancer |
title_sort | disseminated tumour cells as a prognostic biomarker in colorectal cancer |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3101945/ https://www.ncbi.nlm.nih.gov/pubmed/21448171 http://dx.doi.org/10.1038/bjc.2011.97 |
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