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MiSelect R System: the validation of a new detection system of CTCs and their correlation with prognosis in non-metastatic CRC patients

Circulating tumor cells (CTCs) in blood are accepted as a prognostic marker for patients with metastatic colorectal cancer (CRC). However, there is limited data on the use of CTCs as a prognostic marker for non-metastatic patients. In the current study, we used a rare cell automated analysis platfor...

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Autores principales: Lin, Chun-Chi, Yang, Chih-Yung, Hung, Tzu-Chao, Wang, Chun-Hung, Wei, Sheng-Wen, Schiro, Perry, Tseng, Ju-Yu, Lin, Chi-Hung, Jiang, Jeng-Kai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036555/
https://www.ncbi.nlm.nih.gov/pubmed/36959311
http://dx.doi.org/10.1038/s41598-023-31346-9
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author Lin, Chun-Chi
Yang, Chih-Yung
Hung, Tzu-Chao
Wang, Chun-Hung
Wei, Sheng-Wen
Schiro, Perry
Tseng, Ju-Yu
Lin, Chi-Hung
Jiang, Jeng-Kai
author_facet Lin, Chun-Chi
Yang, Chih-Yung
Hung, Tzu-Chao
Wang, Chun-Hung
Wei, Sheng-Wen
Schiro, Perry
Tseng, Ju-Yu
Lin, Chi-Hung
Jiang, Jeng-Kai
author_sort Lin, Chun-Chi
collection PubMed
description Circulating tumor cells (CTCs) in blood are accepted as a prognostic marker for patients with metastatic colorectal cancer (CRC). However, there is limited data on the use of CTCs as a prognostic marker for non-metastatic patients. In the current study, we used a rare cell automated analysis platform, the MiSelect R System, to enumerate CTCs from blood in non-metastatic CRC patients, and corelated the number of CTCs with the clinical staging and survival. The presence of CTCs in mesenteric vein blood (MVB) samples from 101 CRC patients was significantly associated with T stage. Patients with 1 or more CTCs per 8 mL of MVB exhibited significantly worse disease-free survival (DFS) and cancer-specific survival (CSS) compared to patient without CTCs. The presence of CTCs before surgery is an independent marker for both DFS and CSS. CTC presence after surgical resection is also a prognostic marker. CTCs are a potentially useful prognostic and predictive biomarker in non-metastatic CRC patients that may further stratify patient’s risk status within different stages of disease.
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spelling pubmed-100365552023-03-25 MiSelect R System: the validation of a new detection system of CTCs and their correlation with prognosis in non-metastatic CRC patients Lin, Chun-Chi Yang, Chih-Yung Hung, Tzu-Chao Wang, Chun-Hung Wei, Sheng-Wen Schiro, Perry Tseng, Ju-Yu Lin, Chi-Hung Jiang, Jeng-Kai Sci Rep Article Circulating tumor cells (CTCs) in blood are accepted as a prognostic marker for patients with metastatic colorectal cancer (CRC). However, there is limited data on the use of CTCs as a prognostic marker for non-metastatic patients. In the current study, we used a rare cell automated analysis platform, the MiSelect R System, to enumerate CTCs from blood in non-metastatic CRC patients, and corelated the number of CTCs with the clinical staging and survival. The presence of CTCs in mesenteric vein blood (MVB) samples from 101 CRC patients was significantly associated with T stage. Patients with 1 or more CTCs per 8 mL of MVB exhibited significantly worse disease-free survival (DFS) and cancer-specific survival (CSS) compared to patient without CTCs. The presence of CTCs before surgery is an independent marker for both DFS and CSS. CTC presence after surgical resection is also a prognostic marker. CTCs are a potentially useful prognostic and predictive biomarker in non-metastatic CRC patients that may further stratify patient’s risk status within different stages of disease. Nature Publishing Group UK 2023-03-23 /pmc/articles/PMC10036555/ /pubmed/36959311 http://dx.doi.org/10.1038/s41598-023-31346-9 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Lin, Chun-Chi
Yang, Chih-Yung
Hung, Tzu-Chao
Wang, Chun-Hung
Wei, Sheng-Wen
Schiro, Perry
Tseng, Ju-Yu
Lin, Chi-Hung
Jiang, Jeng-Kai
MiSelect R System: the validation of a new detection system of CTCs and their correlation with prognosis in non-metastatic CRC patients
title MiSelect R System: the validation of a new detection system of CTCs and their correlation with prognosis in non-metastatic CRC patients
title_full MiSelect R System: the validation of a new detection system of CTCs and their correlation with prognosis in non-metastatic CRC patients
title_fullStr MiSelect R System: the validation of a new detection system of CTCs and their correlation with prognosis in non-metastatic CRC patients
title_full_unstemmed MiSelect R System: the validation of a new detection system of CTCs and their correlation with prognosis in non-metastatic CRC patients
title_short MiSelect R System: the validation of a new detection system of CTCs and their correlation with prognosis in non-metastatic CRC patients
title_sort miselect r system: the validation of a new detection system of ctcs and their correlation with prognosis in non-metastatic crc patients
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10036555/
https://www.ncbi.nlm.nih.gov/pubmed/36959311
http://dx.doi.org/10.1038/s41598-023-31346-9
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