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Evaluation of Two Different Analytical Methods for Circulating Tumor Cell Detection in Peripheral Blood of Patients with Primary Breast Cancer

Background. Evidence is accumulating that circulating tumor cells (CTC) out of peripheral blood can serve as prognostic marker not only in metastatic but also in early breast cancer (BC). Various methods are available to detect CTC. Comparisons between the different techniques, however, are rare. Ma...

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Autores principales: Jaeger, B. A. S., Jueckstock, J., Andergassen, U., Salmen, J., Schochter, F., Fink, V., Alunni-Fabbroni, M., Rezai, M., Beck, Th., Beckmann, M. W., Friese, K., Friedl, T. W. P., Janni, W., Rack, B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3997081/
https://www.ncbi.nlm.nih.gov/pubmed/24800234
http://dx.doi.org/10.1155/2014/491459
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author Jaeger, B. A. S.
Jueckstock, J.
Andergassen, U.
Salmen, J.
Schochter, F.
Fink, V.
Alunni-Fabbroni, M.
Rezai, M.
Beck, Th.
Beckmann, M. W.
Friese, K.
Friedl, T. W. P.
Janni, W.
Rack, B.
author_facet Jaeger, B. A. S.
Jueckstock, J.
Andergassen, U.
Salmen, J.
Schochter, F.
Fink, V.
Alunni-Fabbroni, M.
Rezai, M.
Beck, Th.
Beckmann, M. W.
Friese, K.
Friedl, T. W. P.
Janni, W.
Rack, B.
author_sort Jaeger, B. A. S.
collection PubMed
description Background. Evidence is accumulating that circulating tumor cells (CTC) out of peripheral blood can serve as prognostic marker not only in metastatic but also in early breast cancer (BC). Various methods are available to detect CTC. Comparisons between the different techniques, however, are rare. Material and Methods. We evaluate two different methods for CTC enrichment and detection in primary BC patients: the FDA-approved CellSearch System (CSS; Veridex, Warren, USA) and a manual immunocytochemistry (MICC). The cut-off value for positivity was ≥1 CTC. Results. The two different nonoverlapping patient cohorts evaluated with one or the other method were well balanced regarding common clinical parameters. Before adjuvant CHT 21.1% (416 out of 1972) and 20.6% (247 out of 1198) of the patients were CTC-positive, while after CHT 22.5% (359 out of 1598) and 16.6% (177 out of 1066) of the patients were CTC-positive using CSS or MICC, respectively. CTC positivity rate before CHT was thus similar and not significantly different (P = 0.749), while CTC positivity rate immediately after CHT was significantly lower using MICC compared to CSS (P < 0.001). Conclusion. Using CSS or MICC for CTC detection, we found comparable prevalence of CTC before but not after adjuvant CHT.
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spelling pubmed-39970812014-05-05 Evaluation of Two Different Analytical Methods for Circulating Tumor Cell Detection in Peripheral Blood of Patients with Primary Breast Cancer Jaeger, B. A. S. Jueckstock, J. Andergassen, U. Salmen, J. Schochter, F. Fink, V. Alunni-Fabbroni, M. Rezai, M. Beck, Th. Beckmann, M. W. Friese, K. Friedl, T. W. P. Janni, W. Rack, B. Biomed Res Int Research Article Background. Evidence is accumulating that circulating tumor cells (CTC) out of peripheral blood can serve as prognostic marker not only in metastatic but also in early breast cancer (BC). Various methods are available to detect CTC. Comparisons between the different techniques, however, are rare. Material and Methods. We evaluate two different methods for CTC enrichment and detection in primary BC patients: the FDA-approved CellSearch System (CSS; Veridex, Warren, USA) and a manual immunocytochemistry (MICC). The cut-off value for positivity was ≥1 CTC. Results. The two different nonoverlapping patient cohorts evaluated with one or the other method were well balanced regarding common clinical parameters. Before adjuvant CHT 21.1% (416 out of 1972) and 20.6% (247 out of 1198) of the patients were CTC-positive, while after CHT 22.5% (359 out of 1598) and 16.6% (177 out of 1066) of the patients were CTC-positive using CSS or MICC, respectively. CTC positivity rate before CHT was thus similar and not significantly different (P = 0.749), while CTC positivity rate immediately after CHT was significantly lower using MICC compared to CSS (P < 0.001). Conclusion. Using CSS or MICC for CTC detection, we found comparable prevalence of CTC before but not after adjuvant CHT. Hindawi Publishing Corporation 2014 2014-04-08 /pmc/articles/PMC3997081/ /pubmed/24800234 http://dx.doi.org/10.1155/2014/491459 Text en Copyright © 2014 B. A. S. Jaeger et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Jaeger, B. A. S.
Jueckstock, J.
Andergassen, U.
Salmen, J.
Schochter, F.
Fink, V.
Alunni-Fabbroni, M.
Rezai, M.
Beck, Th.
Beckmann, M. W.
Friese, K.
Friedl, T. W. P.
Janni, W.
Rack, B.
Evaluation of Two Different Analytical Methods for Circulating Tumor Cell Detection in Peripheral Blood of Patients with Primary Breast Cancer
title Evaluation of Two Different Analytical Methods for Circulating Tumor Cell Detection in Peripheral Blood of Patients with Primary Breast Cancer
title_full Evaluation of Two Different Analytical Methods for Circulating Tumor Cell Detection in Peripheral Blood of Patients with Primary Breast Cancer
title_fullStr Evaluation of Two Different Analytical Methods for Circulating Tumor Cell Detection in Peripheral Blood of Patients with Primary Breast Cancer
title_full_unstemmed Evaluation of Two Different Analytical Methods for Circulating Tumor Cell Detection in Peripheral Blood of Patients with Primary Breast Cancer
title_short Evaluation of Two Different Analytical Methods for Circulating Tumor Cell Detection in Peripheral Blood of Patients with Primary Breast Cancer
title_sort evaluation of two different analytical methods for circulating tumor cell detection in peripheral blood of patients with primary breast cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3997081/
https://www.ncbi.nlm.nih.gov/pubmed/24800234
http://dx.doi.org/10.1155/2014/491459
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