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Updated: Jan 30, 2026

Clinical Microfluidic Chip Platform for the Isolation of Versatile Circulating Tumor Cells
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Capture of Circulating Tumour Cell Clusters Using Straight Microfluidic Chips.

Arutha Kulasinghe1,2, Jian Zhou3,4, Liz Kenny5,6

  • 1The School of Biomedical Sciences, Institute of Health and Biomedical Innovation, Queensland University of Technology, Kelvin Grove, QLD 4059, Australia. arutha.kulasinghe@qut.edu.au.

Cancers
|January 17, 2019
PubMed
Summary

This study introduces a new microfluidic chip for capturing circulating tumor cells (CTCs) and CTC clusters in head and neck cancers. The chip efficiently isolates these cells, revealing EGFR-amplified CTC clusters, which may drive metastasis.

Keywords:
CTC clusterscirculating tumour cells (CTCs)circulating tumour microembolihead and neck cancersmicrofluidic technology

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Area of Science:

  • Oncology
  • Biotechnology
  • Cancer Research

Background:

  • Circulating tumor cells (CTCs) are key indicators of metastasis in head and neck cancers (HNCs).
  • The role of CTC clusters, potentially more metastatic than single CTCs, requires further investigation.
  • Current methods for CTC detection and analysis have limitations.

Purpose of the Study:

  • To develop and validate a novel microfluidic chip for efficient isolation of CTCs, CTC clusters, and circulating tumor microemboli (CTMs) in HNC patients.
  • To investigate the presence and characteristics of CTC subsets in HNC patient samples.
  • To explore the potential metastatic capacity of CTC clusters, particularly regarding EGFR amplification.

Main Methods:

  • Utilization of a novel straight microfluidic chip for focusing and capturing CTCs, CTC clusters, and CTMs.
  • Analysis of 21 HNC patient samples to quantify CTC subsets.
  • Identification and characterization of EGFR amplification within CTC clusters.

Main Results:

  • The microfluidic chip demonstrated high cell recovery rates for CTCs and CTC clusters at clinically relevant concentrations (10-500 cells/mL).
  • Single CTCs were detected in 10/21 samples, CTC clusters in 9/21 samples, and CTMs in 2/21 samples.
  • CTC clusters were found to contain single CTCs with EGFR amplification.

Conclusions:

  • The novel microfluidic chip enables efficient sorting and preservation of CTCs, CTC clusters, and CTMs.
  • CTC clusters, containing EGFR-amplified cells, represent a significant subset in HNC.
  • Further studies with larger cohorts are warranted to elucidate the clinical implications of these CTC subsets in HNC metastasis.