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

Abstract 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 analysi...

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Main Authors: Chun-Chi Lin, Chih-Yung Yang, Tzu-Chao Hung, Chun-Hung Wang, Sheng-Wen Wei, Perry Schiro, Ju-Yu Tseng, Chi-Hung Lin, Jeng-Kai Jiang
Format: Article
Language:English
Published: Nature Portfolio 2023-03-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-31346-9
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author Chun-Chi Lin
Chih-Yung Yang
Tzu-Chao Hung
Chun-Hung Wang
Sheng-Wen Wei
Perry Schiro
Ju-Yu Tseng
Chi-Hung Lin
Jeng-Kai Jiang
author_facet Chun-Chi Lin
Chih-Yung Yang
Tzu-Chao Hung
Chun-Hung Wang
Sheng-Wen Wei
Perry Schiro
Ju-Yu Tseng
Chi-Hung Lin
Jeng-Kai Jiang
author_sort Chun-Chi Lin
collection DOAJ
description Abstract 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 doaj.art-214eeb6d4ce14cc9bd9b103ac0a2514c2023-03-26T11:09:47ZengNature PortfolioScientific Reports2045-23222023-03-0113111010.1038/s41598-023-31346-9MiSelect R System: the validation of a new detection system of CTCs and their correlation with prognosis in non-metastatic CRC patientsChun-Chi Lin0Chih-Yung Yang1Tzu-Chao Hung2Chun-Hung Wang3Sheng-Wen Wei4Perry Schiro5Ju-Yu Tseng6Chi-Hung Lin7Jeng-Kai Jiang8Division of Colon and Rectal Surgery, Department of Surgery, Taipei Veterans General HospitalDepartment of Teaching and Research, Taipei City HospitalMiCareo Taiwan Co., Ltd.MiCareo Taiwan Co., Ltd.MiCareo Taiwan Co., Ltd.MiCareo Taiwan Co., Ltd.MiCareo Taiwan Co., Ltd.Department of Biological Science and Technology, National Yang-Ming Chiao-Tung UniversityDivision of Colon and Rectal Surgery, Department of Surgery, Taipei Veterans General HospitalAbstract 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.https://doi.org/10.1038/s41598-023-31346-9
spellingShingle Chun-Chi Lin
Chih-Yung Yang
Tzu-Chao Hung
Chun-Hung Wang
Sheng-Wen Wei
Perry Schiro
Ju-Yu Tseng
Chi-Hung Lin
Jeng-Kai Jiang
MiSelect R System: the validation of a new detection system of CTCs and their correlation with prognosis in non-metastatic CRC patients
Scientific Reports
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
url https://doi.org/10.1038/s41598-023-31346-9
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