Cytokeratin-based CTC counting unrelated to clinical follow up
Circulating tumor cells (CTCs) have been reported to be a relevant prognostic biomarker in metastatic patients. However, their clinical use and impact is still under debate. We have thus comparatively and kinetically assessed two CTC detection methods according to the patient's clinical follow...
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Veröffentlicht in: | Journal of thoracic disease 2013-10, Vol.5 (5), p.593-599 |
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creator | Chinen, Ludmilla Thomé Domingos de Carvalho, Fernanda Machado Rocha, Bruna Maria Malagoli Aguiar, Caroline Motta Abdallah, Emne Ali Campanha, Daniel Mingues, Natália Breve de Oliveira, Thiago Bueno Maciel, Macello Sampaio Cervantes, Gustavo Marchioro Dettino, Aldo L A Soares, Fernando Augusto Paterlini-Bréchot, Patrizia Fanelli, Marcello Ferretti |
description | Circulating tumor cells (CTCs) have been reported to be a relevant prognostic biomarker in metastatic patients. However, their clinical use and impact is still under debate. We have thus comparatively and kinetically assessed two CTC detection methods according to the patient's clinical follow up.
CTC counting and characterization were repeatedly performed during follow up in a patient with metastatic undifferentiated non-small cell lung cancer by using cytokeratin (CK)-dependent immunomagnetic separation (Miltenyi) and CK-independent, size-based isolation [isolation by size of tumor cells (ISET)] (Rarecells).
Comparison between the two methods showed a parallel increase of CTC detected by ISET and worsening of the clinical status, while CK-dependent CTC numbers were decreasing, misleadingly suggesting a response to treatment. ISET results were in agreement with the clinical follow up showing Circulating tumor microemboli (CTM) and CTC expressing a mesenchymal marker with absence of epithelial markers.
This case report study shows the interest of a comparative and kinetic analysis of different methods for CTCs detection combined with their evaluation according to the clinical follow up. Our results should open up an area for future research and validation in larger clinical cohorts. |
doi_str_mv | 10.3978/j.issn.2072-1439.2013.09.18 |
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CTC counting and characterization were repeatedly performed during follow up in a patient with metastatic undifferentiated non-small cell lung cancer by using cytokeratin (CK)-dependent immunomagnetic separation (Miltenyi) and CK-independent, size-based isolation [isolation by size of tumor cells (ISET)] (Rarecells).
Comparison between the two methods showed a parallel increase of CTC detected by ISET and worsening of the clinical status, while CK-dependent CTC numbers were decreasing, misleadingly suggesting a response to treatment. ISET results were in agreement with the clinical follow up showing Circulating tumor microemboli (CTM) and CTC expressing a mesenchymal marker with absence of epithelial markers.
This case report study shows the interest of a comparative and kinetic analysis of different methods for CTCs detection combined with their evaluation according to the clinical follow up. Our results should open up an area for future research and validation in larger clinical cohorts.</description><identifier>ISSN: 2072-1439</identifier><identifier>EISSN: 2077-6624</identifier><identifier>DOI: 10.3978/j.issn.2072-1439.2013.09.18</identifier><identifier>PMID: 24255771</identifier><language>eng</language><publisher>China: Pioneer Bioscience Publishing Company</publisher><subject>Original</subject><ispartof>Journal of thoracic disease, 2013-10, Vol.5 (5), p.593-599</ispartof><rights>2013 Pioneer Bioscience Publishing Company. All rights reserved. 2013 Pioneer Bioscience Publishing Company.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c324t-9aeb397160a0dc79fa2495dfe676ecc3e26b9a9c3edbee619f7731c995180a973</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815714/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815714/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24255771$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chinen, Ludmilla Thomé Domingos</creatorcontrib><creatorcontrib>de Carvalho, Fernanda Machado</creatorcontrib><creatorcontrib>Rocha, Bruna Maria Malagoli</creatorcontrib><creatorcontrib>Aguiar, Caroline Motta</creatorcontrib><creatorcontrib>Abdallah, Emne Ali</creatorcontrib><creatorcontrib>Campanha, Daniel</creatorcontrib><creatorcontrib>Mingues, Natália Breve</creatorcontrib><creatorcontrib>de Oliveira, Thiago Bueno</creatorcontrib><creatorcontrib>Maciel, Macello Sampaio</creatorcontrib><creatorcontrib>Cervantes, Gustavo Marchioro</creatorcontrib><creatorcontrib>Dettino, Aldo L A</creatorcontrib><creatorcontrib>Soares, Fernando Augusto</creatorcontrib><creatorcontrib>Paterlini-Bréchot, Patrizia</creatorcontrib><creatorcontrib>Fanelli, Marcello Ferretti</creatorcontrib><title>Cytokeratin-based CTC counting unrelated to clinical follow up</title><title>Journal of thoracic disease</title><addtitle>J Thorac Dis</addtitle><description>Circulating tumor cells (CTCs) have been reported to be a relevant prognostic biomarker in metastatic patients. However, their clinical use and impact is still under debate. We have thus comparatively and kinetically assessed two CTC detection methods according to the patient's clinical follow up.
CTC counting and characterization were repeatedly performed during follow up in a patient with metastatic undifferentiated non-small cell lung cancer by using cytokeratin (CK)-dependent immunomagnetic separation (Miltenyi) and CK-independent, size-based isolation [isolation by size of tumor cells (ISET)] (Rarecells).
Comparison between the two methods showed a parallel increase of CTC detected by ISET and worsening of the clinical status, while CK-dependent CTC numbers were decreasing, misleadingly suggesting a response to treatment. ISET results were in agreement with the clinical follow up showing Circulating tumor microemboli (CTM) and CTC expressing a mesenchymal marker with absence of epithelial markers.
This case report study shows the interest of a comparative and kinetic analysis of different methods for CTCs detection combined with their evaluation according to the clinical follow up. Our results should open up an area for future research and validation in larger clinical cohorts.</description><subject>Original</subject><issn>2072-1439</issn><issn>2077-6624</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNpVUF1LwzAUDaK4MfcXpOCLL635aJPmZSDFLxj4Mp9Lmt7OzCyZTavs3xvcFL0v93Du4ZzLQeiK4IxJUd5sMhOCyygWNCU5kxERlmGZkfIETSMtUs5pfvqND5IJmoewwXE4plSIczShOS0KIcgULar94N-gV4NxaaMCtEm1qhLtRxeZdTK6HqwaIj34RFvjjFY26by1_jMZdxforFM2wPy4Z-jl_m5VPabL54en6naZakbzIZUKmvg-4VjhVgvZKZrLou2ACw5aM6C8kUpG0DYAnMhOCEa0lAUpsZKCzdDi4Lsbmy20GtzQK1vverNV_b72ytT_L8681mv_UbOSFCK2MEPXR4Pev48QhnprggZrlQM_hprkXFJcYl5G6eXfrN-Qn9LYF7LBc3U</recordid><startdate>201310</startdate><enddate>201310</enddate><creator>Chinen, Ludmilla Thomé Domingos</creator><creator>de Carvalho, Fernanda Machado</creator><creator>Rocha, Bruna Maria Malagoli</creator><creator>Aguiar, Caroline Motta</creator><creator>Abdallah, Emne Ali</creator><creator>Campanha, Daniel</creator><creator>Mingues, Natália Breve</creator><creator>de Oliveira, Thiago Bueno</creator><creator>Maciel, Macello Sampaio</creator><creator>Cervantes, Gustavo Marchioro</creator><creator>Dettino, Aldo L A</creator><creator>Soares, Fernando Augusto</creator><creator>Paterlini-Bréchot, Patrizia</creator><creator>Fanelli, Marcello Ferretti</creator><general>Pioneer Bioscience Publishing Company</general><scope>NPM</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>201310</creationdate><title>Cytokeratin-based CTC counting unrelated to clinical follow up</title><author>Chinen, Ludmilla Thomé Domingos ; de Carvalho, Fernanda Machado ; Rocha, Bruna Maria Malagoli ; Aguiar, Caroline Motta ; Abdallah, Emne Ali ; Campanha, Daniel ; Mingues, Natália Breve ; de Oliveira, Thiago Bueno ; Maciel, Macello Sampaio ; Cervantes, Gustavo Marchioro ; Dettino, Aldo L A ; Soares, Fernando Augusto ; Paterlini-Bréchot, Patrizia ; Fanelli, Marcello Ferretti</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c324t-9aeb397160a0dc79fa2495dfe676ecc3e26b9a9c3edbee619f7731c995180a973</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Original</topic><toplevel>online_resources</toplevel><creatorcontrib>Chinen, Ludmilla Thomé Domingos</creatorcontrib><creatorcontrib>de Carvalho, Fernanda Machado</creatorcontrib><creatorcontrib>Rocha, Bruna Maria Malagoli</creatorcontrib><creatorcontrib>Aguiar, Caroline Motta</creatorcontrib><creatorcontrib>Abdallah, Emne Ali</creatorcontrib><creatorcontrib>Campanha, Daniel</creatorcontrib><creatorcontrib>Mingues, Natália Breve</creatorcontrib><creatorcontrib>de Oliveira, Thiago Bueno</creatorcontrib><creatorcontrib>Maciel, Macello Sampaio</creatorcontrib><creatorcontrib>Cervantes, Gustavo Marchioro</creatorcontrib><creatorcontrib>Dettino, Aldo L A</creatorcontrib><creatorcontrib>Soares, Fernando Augusto</creatorcontrib><creatorcontrib>Paterlini-Bréchot, Patrizia</creatorcontrib><creatorcontrib>Fanelli, Marcello Ferretti</creatorcontrib><collection>PubMed</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of thoracic disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chinen, Ludmilla Thomé Domingos</au><au>de Carvalho, Fernanda Machado</au><au>Rocha, Bruna Maria Malagoli</au><au>Aguiar, Caroline Motta</au><au>Abdallah, Emne Ali</au><au>Campanha, Daniel</au><au>Mingues, Natália Breve</au><au>de Oliveira, Thiago Bueno</au><au>Maciel, Macello Sampaio</au><au>Cervantes, Gustavo Marchioro</au><au>Dettino, Aldo L A</au><au>Soares, Fernando Augusto</au><au>Paterlini-Bréchot, Patrizia</au><au>Fanelli, Marcello Ferretti</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cytokeratin-based CTC counting unrelated to clinical follow up</atitle><jtitle>Journal of thoracic disease</jtitle><addtitle>J Thorac Dis</addtitle><date>2013-10</date><risdate>2013</risdate><volume>5</volume><issue>5</issue><spage>593</spage><epage>599</epage><pages>593-599</pages><issn>2072-1439</issn><eissn>2077-6624</eissn><abstract>Circulating tumor cells (CTCs) have been reported to be a relevant prognostic biomarker in metastatic patients. However, their clinical use and impact is still under debate. We have thus comparatively and kinetically assessed two CTC detection methods according to the patient's clinical follow up.
CTC counting and characterization were repeatedly performed during follow up in a patient with metastatic undifferentiated non-small cell lung cancer by using cytokeratin (CK)-dependent immunomagnetic separation (Miltenyi) and CK-independent, size-based isolation [isolation by size of tumor cells (ISET)] (Rarecells).
Comparison between the two methods showed a parallel increase of CTC detected by ISET and worsening of the clinical status, while CK-dependent CTC numbers were decreasing, misleadingly suggesting a response to treatment. ISET results were in agreement with the clinical follow up showing Circulating tumor microemboli (CTM) and CTC expressing a mesenchymal marker with absence of epithelial markers.
This case report study shows the interest of a comparative and kinetic analysis of different methods for CTCs detection combined with their evaluation according to the clinical follow up. Our results should open up an area for future research and validation in larger clinical cohorts.</abstract><cop>China</cop><pub>Pioneer Bioscience Publishing Company</pub><pmid>24255771</pmid><doi>10.3978/j.issn.2072-1439.2013.09.18</doi><tpages>7</tpages></addata></record> |
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title | Cytokeratin-based CTC counting unrelated to clinical follow up |
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