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Isolated tumor cells in stage I & II colon cancer patients are associated with significantly worse disease-free and overall survival
BACKGROUND: Lymph node (LN) involvement represents the strongest prognostic factor in colon cancer patients. The objective of this prospective study was to assess the prognostic impact of isolated tumor cells (ITC, defined as cell deposits ≤ 0.2 mm) in loco-regional LN of stage I & II colon canc...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754888/ https://www.ncbi.nlm.nih.gov/pubmed/26879046 http://dx.doi.org/10.1186/s12885-016-2130-7 |
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author | Weixler, B. Warschkow, R. Güller, U. Zettl, A. von Holzen, U. Schmied, B. M. Zuber, M. |
author_facet | Weixler, B. Warschkow, R. Güller, U. Zettl, A. von Holzen, U. Schmied, B. M. Zuber, M. |
author_sort | Weixler, B. |
collection | PubMed |
description | BACKGROUND: Lymph node (LN) involvement represents the strongest prognostic factor in colon cancer patients. The objective of this prospective study was to assess the prognostic impact of isolated tumor cells (ITC, defined as cell deposits ≤ 0.2 mm) in loco-regional LN of stage I & II colon cancer patients. METHODS: Seventy-four stage I & II colon cancer patients were prospectively enrolled in the present study. LN at high risk of harboring ITC were identified via an in vivo sentinel lymph node procedure and analyzed with multilevel sectioning, conventional H&E and immunohistochemical CK-19 staining. The impact of ITC on survival was assessed using Cox regression analyses. RESULTS: Median follow-up was 4.6 years. ITC were detected in locoregional lymph nodes of 23 patients (31.1 %). The presence of ITC was associated with a significantly worse disease-free survival (hazard ratio = 4.73, p = 0.005). Similarly, ITC were associated with significantly worse overall survival (hazard ratio = 3.50, p = 0.043). CONCLUSIONS: This study provides compelling evidence that ITC in stage I & II colon cancer patients are associated with significantly worse disease-free and overall survival. Based on these data, the presence of ITC should be classified as a high risk factor in stage I & II colon cancer patients who might benefit from adjuvant chemotherapy. |
format | Online Article Text |
id | pubmed-4754888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-47548882016-02-17 Isolated tumor cells in stage I & II colon cancer patients are associated with significantly worse disease-free and overall survival Weixler, B. Warschkow, R. Güller, U. Zettl, A. von Holzen, U. Schmied, B. M. Zuber, M. BMC Cancer Research Article BACKGROUND: Lymph node (LN) involvement represents the strongest prognostic factor in colon cancer patients. The objective of this prospective study was to assess the prognostic impact of isolated tumor cells (ITC, defined as cell deposits ≤ 0.2 mm) in loco-regional LN of stage I & II colon cancer patients. METHODS: Seventy-four stage I & II colon cancer patients were prospectively enrolled in the present study. LN at high risk of harboring ITC were identified via an in vivo sentinel lymph node procedure and analyzed with multilevel sectioning, conventional H&E and immunohistochemical CK-19 staining. The impact of ITC on survival was assessed using Cox regression analyses. RESULTS: Median follow-up was 4.6 years. ITC were detected in locoregional lymph nodes of 23 patients (31.1 %). The presence of ITC was associated with a significantly worse disease-free survival (hazard ratio = 4.73, p = 0.005). Similarly, ITC were associated with significantly worse overall survival (hazard ratio = 3.50, p = 0.043). CONCLUSIONS: This study provides compelling evidence that ITC in stage I & II colon cancer patients are associated with significantly worse disease-free and overall survival. Based on these data, the presence of ITC should be classified as a high risk factor in stage I & II colon cancer patients who might benefit from adjuvant chemotherapy. BioMed Central 2016-02-16 /pmc/articles/PMC4754888/ /pubmed/26879046 http://dx.doi.org/10.1186/s12885-016-2130-7 Text en © Weixler et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Weixler, B. Warschkow, R. Güller, U. Zettl, A. von Holzen, U. Schmied, B. M. Zuber, M. Isolated tumor cells in stage I & II colon cancer patients are associated with significantly worse disease-free and overall survival |
title | Isolated tumor cells in stage I & II colon cancer patients are associated with significantly worse disease-free and overall survival |
title_full | Isolated tumor cells in stage I & II colon cancer patients are associated with significantly worse disease-free and overall survival |
title_fullStr | Isolated tumor cells in stage I & II colon cancer patients are associated with significantly worse disease-free and overall survival |
title_full_unstemmed | Isolated tumor cells in stage I & II colon cancer patients are associated with significantly worse disease-free and overall survival |
title_short | Isolated tumor cells in stage I & II colon cancer patients are associated with significantly worse disease-free and overall survival |
title_sort | isolated tumor cells in stage i & ii colon cancer patients are associated with significantly worse disease-free and overall survival |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754888/ https://www.ncbi.nlm.nih.gov/pubmed/26879046 http://dx.doi.org/10.1186/s12885-016-2130-7 |
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