Abstract

Circulating tumor cell (CTC) count is an independent prognostic factor in early breast cancer. CTCs can be found in the blood of 20% of patients prior to neoadjuvant therapy. We aimed to assess the suitability of magnetic-activated cell separation (MACS) technology for isolation and cytological characterization of CTCs. In the preclinical part of the study, cell lines were spiked into buffy coat samples derived from healthy donors, and isolated using MACS. Breast cancer cells with preserved cell morphology were successfully isolated. In the clinical part, blood for CTC isolation was drawn from 44 patients with early and locally advanced breast cancer prior to neoadjuvant chemotherapy. Standard Giemsa, Papanicolaou and pancytokeratin staining was applied. 2.3% of samples contained cells that meet both the morphological and immunocytochemical criteria for CTC. In 32.6% of samples, partially degenerated pancytokeratin negative cells with morphological features of tumor cells were observed. In 65.1% of samples, CTCs were not found. In conclusion, our results demonstrate that morphologically intact tumor cells can be isolated using MACS technology. However, morphologically intact tumor cells were not detected in the clinical part of the study. At present, MACS technology does not appear suitable for use in a clinical cytopathology laboratory.

Highlights

  • Circulating tumor cells (CTCs) are believed to be an intermediate step in the metastatic cascade

  • To evaluate the method’s sensitivity, 14 buffy coat (BC) samples were spiked with Michigan Cancer Foundation 7 (MCF7) cells and examined before and after the magnetic-activated cell separation (MACS) isolation procedure

  • This study aimed to evaluate the feasibility of the MACS technology for CTC isolation and subsequent cytopathological examination in the routine cytopathological laboratory setting in early breast cancer

Read more

Summary

Introduction

Circulating tumor cells (CTCs) are believed to be an intermediate step in the metastatic cascade. During growth of the primary or metastatic tumor, epithelial tumor cells may leave the tumor site, invade into a blood or lymphatic vessel and circulate in the bloodstream to disseminate throughout the body, potentially becoming the source of cancer metastases [1, 2]. CTC detection before neoadjuvant setting carries an independent negative prognostic value for a reduced disease-free and overall survival [29], while not being associated with pathologic complete response [25, 30]. Taken together, this data indicates that breast cancer patients before neoadjuvant setting may represent a population that might benefit most from CTC diagnostics

Objectives
Methods
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call