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Updated: Apr 3, 2026

Micromanipulation of Circulating Tumor Cells for Downstream Molecular Analysis and Metastatic Potential Assessment
Published on: May 14, 2019
Circulating Tumor Cell Analyses in Patients With Esophageal Squamous Cell Carcinoma Using Epithelial Marker-Dependent
Hao Li1, Pingping Song, Benkui Zou
1From the Department of Interventional Radiology (HL), Shandong Provincial Qianfoshan Hospital, Shandong University, Jinan, Shandong; Shandong Cancer Hospital and Institute (HL), Jinan, Shandong; Department of Thoracic Surgery (PS, BZ), Shandong Cancer Hospital and Institute, Jinan, Shandong; Department of Urology (BZ), Shandong Cancer Hospital and Institute, Jinan, Shandong; Department of Clinical Laboratory (ML), Shandong Cancer Hospital and Institute, Jinan, Shandong; Department of Hepatobiliary Surgery (KC, SL), Shandong Cancer Hospital and Institute, Jinan, Shandong; Wuhan YZY Medical Science & Technology Co. Ltd (PZ), Wuhan, Hubei; and Shandong Provincial Collaborative Innovation Center for Neurodegenerative Disorders (SL), Qingdao University, Qingdao, Shandong, China.
Abstract:
In several epithelial malignancies, detection of circulating tumor cells (CTCs) in the peripheral blood has diagnostic, prognostic, and therapeutic implications. However, the clinical relevance of CTCs in esophageal squamous cell carcinoma (ESCC) has not yet been ascertained. The study was conducted with the aim of determining the clinical significance of CTCs in patients with ESCC by using 2 CTC detection systems, one epithelial marker-dependent and the other epithelial marker-independent. Paired peripheral blood samples were prospectively obtained from 61 ESCC patients before treatment and were analyzed for CTCs isolated by the CellSearch system (CS) and the method of isolation by size of epithelial tumor (ISET). Blood samples from 22 healthy volunteers were used as controls. Out of 61 study subjects, CTCs were detected in 20 patients (32.8%) by the ISET method and in only 1 patient (1.6%) by the CS method. Circulating tumor microemboli (CTM) were observed in 3 of 61 (4.9%) patients using ISET, but were undetectable in any of the patient by CS method. No CTCs/CTM were detected by either method in control groups. By ISET method, the presence of CTCs appeared to correlate with the stage of ESCC and with the baseline median platelet levels. No correlation with any other relevant clinicopathological variables was observed. Our results clearly indicate the ability of both CS and ISET methods to detect CTCs in peripheral blood samples from ESCC patients. However, the CellSearch system appears to have a poorer sensitivity as compared with the ISET method. Further studies are essential for assessing the role of such technologies in ESCC.
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