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Quantifying HER-2 expression on circulating tumor cells by ACCEPT

Circulating tumor cells (CTCs) isolated from blood can be probed for the expression of treatment targets. Immunofluorescence is often used for both the enumeration of CTC and the determination of protein expression levels related to treatment targets. Accurate and reproducible assessment of such tre...

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Autores principales: Zeune, Leonie, van Dalum, Guus, Decraene, Charles, Proudhon, Charlotte, Fehm, Tanja, Neubauer, Hans, Rack, Brigitte, Alunni-Fabbroni, Marianna, Terstappen, Leon W. M. M., van Gils, Stephan A., Brune, Christoph
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662084/
https://www.ncbi.nlm.nih.gov/pubmed/29084234
http://dx.doi.org/10.1371/journal.pone.0186562
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author Zeune, Leonie
van Dalum, Guus
Decraene, Charles
Proudhon, Charlotte
Fehm, Tanja
Neubauer, Hans
Rack, Brigitte
Alunni-Fabbroni, Marianna
Terstappen, Leon W. M. M.
van Gils, Stephan A.
Brune, Christoph
author_facet Zeune, Leonie
van Dalum, Guus
Decraene, Charles
Proudhon, Charlotte
Fehm, Tanja
Neubauer, Hans
Rack, Brigitte
Alunni-Fabbroni, Marianna
Terstappen, Leon W. M. M.
van Gils, Stephan A.
Brune, Christoph
author_sort Zeune, Leonie
collection PubMed
description Circulating tumor cells (CTCs) isolated from blood can be probed for the expression of treatment targets. Immunofluorescence is often used for both the enumeration of CTC and the determination of protein expression levels related to treatment targets. Accurate and reproducible assessment of such treatment target expression levels is essential for their use in the clinic. To enable this, an open source image analysis program named ACCEPT was developed in the EU-FP7 CTCTrap and CANCER-ID programs. Here its application is shown on a retrospective cohort of 132 metastatic breast cancer patients from which blood samples were processed by CellSearch(®) and stained for HER-2 expression as additional marker. Images were digitally stored and reviewers identified a total of 4084 CTCs. CTC’s HER-2 expression was determined in the thumbnail images by ACCEPT. 150 of these images were selected and sent to six independent investigators to score the HER-2 expression with and without ACCEPT. Concordance rate of the operators’ scoring results for HER-2 on CTCs was 30% and could be increased using the ACCEPT tool to 51%. Automated assessment of HER-2 expression by ACCEPT on 4084 CTCs of 132 patients showed 8 (6.1%) patients with all CTCs expressing HER-2, 14 (10.6%) patients with no CTC expressing HER-2 and 110 (83.3%) patients with CTCs showing a varying HER-2 expression level. In total 1576 CTCs were determined HER-2 positive. We conclude that the use of image analysis enables a more reproducible quantification of treatment targets on CTCs and leads the way to fully automated and reproducible approaches.
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spelling pubmed-56620842017-11-09 Quantifying HER-2 expression on circulating tumor cells by ACCEPT Zeune, Leonie van Dalum, Guus Decraene, Charles Proudhon, Charlotte Fehm, Tanja Neubauer, Hans Rack, Brigitte Alunni-Fabbroni, Marianna Terstappen, Leon W. M. M. van Gils, Stephan A. Brune, Christoph PLoS One Research Article Circulating tumor cells (CTCs) isolated from blood can be probed for the expression of treatment targets. Immunofluorescence is often used for both the enumeration of CTC and the determination of protein expression levels related to treatment targets. Accurate and reproducible assessment of such treatment target expression levels is essential for their use in the clinic. To enable this, an open source image analysis program named ACCEPT was developed in the EU-FP7 CTCTrap and CANCER-ID programs. Here its application is shown on a retrospective cohort of 132 metastatic breast cancer patients from which blood samples were processed by CellSearch(®) and stained for HER-2 expression as additional marker. Images were digitally stored and reviewers identified a total of 4084 CTCs. CTC’s HER-2 expression was determined in the thumbnail images by ACCEPT. 150 of these images were selected and sent to six independent investigators to score the HER-2 expression with and without ACCEPT. Concordance rate of the operators’ scoring results for HER-2 on CTCs was 30% and could be increased using the ACCEPT tool to 51%. Automated assessment of HER-2 expression by ACCEPT on 4084 CTCs of 132 patients showed 8 (6.1%) patients with all CTCs expressing HER-2, 14 (10.6%) patients with no CTC expressing HER-2 and 110 (83.3%) patients with CTCs showing a varying HER-2 expression level. In total 1576 CTCs were determined HER-2 positive. We conclude that the use of image analysis enables a more reproducible quantification of treatment targets on CTCs and leads the way to fully automated and reproducible approaches. Public Library of Science 2017-10-30 /pmc/articles/PMC5662084/ /pubmed/29084234 http://dx.doi.org/10.1371/journal.pone.0186562 Text en © 2017 Zeune 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
Zeune, Leonie
van Dalum, Guus
Decraene, Charles
Proudhon, Charlotte
Fehm, Tanja
Neubauer, Hans
Rack, Brigitte
Alunni-Fabbroni, Marianna
Terstappen, Leon W. M. M.
van Gils, Stephan A.
Brune, Christoph
Quantifying HER-2 expression on circulating tumor cells by ACCEPT
title Quantifying HER-2 expression on circulating tumor cells by ACCEPT
title_full Quantifying HER-2 expression on circulating tumor cells by ACCEPT
title_fullStr Quantifying HER-2 expression on circulating tumor cells by ACCEPT
title_full_unstemmed Quantifying HER-2 expression on circulating tumor cells by ACCEPT
title_short Quantifying HER-2 expression on circulating tumor cells by ACCEPT
title_sort quantifying her-2 expression on circulating tumor cells by accept
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5662084/
https://www.ncbi.nlm.nih.gov/pubmed/29084234
http://dx.doi.org/10.1371/journal.pone.0186562
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