Portable filter-based microdevice for detection and characterization of circulating tumor cells. Academic Article uri icon

Overview

abstract

  • PURPOSE: Sensitive detection and characterization of circulating tumor cells (CTC) could revolutionize the approach to patients with early-stage and metastatic cancer. The current methodologies have significant limitations, including limited capture efficiency and ability to characterize captured cells. Here, we report the development of a novel parylene membrane filter-based portable microdevice for size-based isolation with high recovery rate and direct on-chip characterization of captured CTC from human peripheral blood. EXPERIMENTAL DESIGN: We evaluated the sensitivity and efficiency of CTC capture in a model system using blood samples from healthy donors spiked with tumor cell lines. Fifty-nine model system samples were tested to determine the recovery rate of the microdevice. Moreover, 10 model system samples and 57 blood samples from cancer patients were subjected to both membrane microfilter device and CellSearch platform enumeration for direct comparison. RESULTS: Using the model system, the microdevice achieved >90% recovery with probability of 95% recovering at least one cell when five are seeded in 7.5 mL of blood. CTCs were identified in 51 of 57 patients using the microdevice, compared with only 26 patients with the CellSearch method. When CTCs were detected by both methods, greater numbers were recovered by the microfilter device in all but five patients. CONCLUSIONS: This filter-based microdevice is both a capture and analysis platform, capable of multiplexed imaging and genetic analysis. The microdevice presented here has the potential to enable routine CTC analysis in the clinical setting for the effective management of cancer patients.

publication date

  • September 28, 2010

Research

keywords

  • Hemofiltration
  • Microfluidic Analytical Techniques
  • Neoplasms
  • Neoplastic Cells, Circulating

Identity

PubMed Central ID

  • PMC2955786

Scopus Document Identifier

  • 77958037272

Digital Object Identifier (DOI)

  • 10.1158/1078-0432.CCR-10-1105

PubMed ID

  • 20876796

Additional Document Info

volume

  • 16

issue

  • 20