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Improved Detection of Circulating Tumor Cells in Metastatic Colorectal Cancer by the Combination of the CellSearch(®) System and the AdnaTest(®)

Colorectal cancer (CRC) is one of the major causes of cancer-related death and reliable blood-based prognostic biomarkers are urgently needed. The enumeration and molecular characterization of circulating tumor cells (CTCs) has gained increasing interest in clinical practice. CTC detection by CellSe...

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Autores principales: Gorges, Tobias M., Stein, Alexander, Quidde, Julia, Hauch, Siegfried, Röck, Katharina, Riethdorf, Sabine, Joosse, Simon A., Pantel, Klaus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868337/
https://www.ncbi.nlm.nih.gov/pubmed/27182774
http://dx.doi.org/10.1371/journal.pone.0155126
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author Gorges, Tobias M.
Stein, Alexander
Quidde, Julia
Hauch, Siegfried
Röck, Katharina
Riethdorf, Sabine
Joosse, Simon A.
Pantel, Klaus
author_facet Gorges, Tobias M.
Stein, Alexander
Quidde, Julia
Hauch, Siegfried
Röck, Katharina
Riethdorf, Sabine
Joosse, Simon A.
Pantel, Klaus
author_sort Gorges, Tobias M.
collection PubMed
description Colorectal cancer (CRC) is one of the major causes of cancer-related death and reliable blood-based prognostic biomarkers are urgently needed. The enumeration and molecular characterization of circulating tumor cells (CTCs) has gained increasing interest in clinical practice. CTC detection by CellSearch(®) has already been correlated to an unfavorable outcome in metastatic CRC. However, the CTC detection rate in mCRC disease is low compared to other tumor entities. Thus, the use of alternative (or supplementary) assays might help to itemize the prognostic use of CTCs as blood-based biomarkers. In this study, blood samples from 47 mCRC patients were screened for CTCs using the FDA-cleared CellSearch(®) technology and / or the AdnaTest(®). 38 samples could be processed in parallel. We demonstrate that a combined analysis of CellSearch(®) and the AdnaTest(®) leads to an improved detection of CTCs in our mCRC patient cohort (positivity rate CellSearch(®) 33%, AdnaTest(®) 30%, combined 50%). While CTCs detected with the CellSearch(®) system were significantly associated with progression-free survival (p = 0.046), a significant correlation regarding overall survival could be only seen when both assays were combined (p = 0.013). These findings could help to establish improved tools to detect CTCs as on-treatment biomarkers for clinical routine in future studies.
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spelling pubmed-48683372016-05-26 Improved Detection of Circulating Tumor Cells in Metastatic Colorectal Cancer by the Combination of the CellSearch(®) System and the AdnaTest(®) Gorges, Tobias M. Stein, Alexander Quidde, Julia Hauch, Siegfried Röck, Katharina Riethdorf, Sabine Joosse, Simon A. Pantel, Klaus PLoS One Research Article Colorectal cancer (CRC) is one of the major causes of cancer-related death and reliable blood-based prognostic biomarkers are urgently needed. The enumeration and molecular characterization of circulating tumor cells (CTCs) has gained increasing interest in clinical practice. CTC detection by CellSearch(®) has already been correlated to an unfavorable outcome in metastatic CRC. However, the CTC detection rate in mCRC disease is low compared to other tumor entities. Thus, the use of alternative (or supplementary) assays might help to itemize the prognostic use of CTCs as blood-based biomarkers. In this study, blood samples from 47 mCRC patients were screened for CTCs using the FDA-cleared CellSearch(®) technology and / or the AdnaTest(®). 38 samples could be processed in parallel. We demonstrate that a combined analysis of CellSearch(®) and the AdnaTest(®) leads to an improved detection of CTCs in our mCRC patient cohort (positivity rate CellSearch(®) 33%, AdnaTest(®) 30%, combined 50%). While CTCs detected with the CellSearch(®) system were significantly associated with progression-free survival (p = 0.046), a significant correlation regarding overall survival could be only seen when both assays were combined (p = 0.013). These findings could help to establish improved tools to detect CTCs as on-treatment biomarkers for clinical routine in future studies. Public Library of Science 2016-05-16 /pmc/articles/PMC4868337/ /pubmed/27182774 http://dx.doi.org/10.1371/journal.pone.0155126 Text en © 2016 Gorges et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Gorges, Tobias M.
Stein, Alexander
Quidde, Julia
Hauch, Siegfried
Röck, Katharina
Riethdorf, Sabine
Joosse, Simon A.
Pantel, Klaus
Improved Detection of Circulating Tumor Cells in Metastatic Colorectal Cancer by the Combination of the CellSearch(®) System and the AdnaTest(®)
title Improved Detection of Circulating Tumor Cells in Metastatic Colorectal Cancer by the Combination of the CellSearch(®) System and the AdnaTest(®)
title_full Improved Detection of Circulating Tumor Cells in Metastatic Colorectal Cancer by the Combination of the CellSearch(®) System and the AdnaTest(®)
title_fullStr Improved Detection of Circulating Tumor Cells in Metastatic Colorectal Cancer by the Combination of the CellSearch(®) System and the AdnaTest(®)
title_full_unstemmed Improved Detection of Circulating Tumor Cells in Metastatic Colorectal Cancer by the Combination of the CellSearch(®) System and the AdnaTest(®)
title_short Improved Detection of Circulating Tumor Cells in Metastatic Colorectal Cancer by the Combination of the CellSearch(®) System and the AdnaTest(®)
title_sort improved detection of circulating tumor cells in metastatic colorectal cancer by the combination of the cellsearch(®) system and the adnatest(®)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4868337/
https://www.ncbi.nlm.nih.gov/pubmed/27182774
http://dx.doi.org/10.1371/journal.pone.0155126
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