Liquid Biopsy Analysis as a Tool for TKI-Based Treatment in Non-Small Cell Lung Cancer

Karolina Buszka1,2, Aliki Ntzifa3, Barbara Owecka1

  • 1Department of Histology and Embryology, Poznan University of Medical Sciences, 60-781 Poznan, Poland.

Cells
|September 23, 2022
PubMed

Insights

Liquid biopsy aids in selecting and monitoring targeted therapy for non-small cell lung cancer (NSCLC) patients with specific gene alterations. This approach, using circulating tumor cells and cell-free DNA, complements tissue biopsies for improved treatment outcomes.

Area of Science:

  • Oncology
  • Molecular Diagnostics
  • Genetics

Background:

  • Targeted therapy with tyrosine kinase inhibitors (TKIs) has advanced non-small cell lung cancer (NSCLC) treatment for patients with specific gene alterations (EGFR, ALK, ROS1, BRAF, MET).
  • TKIs have significantly improved progression-free survival (PFS) in advanced NSCLC.
  • Molecularly targeted therapy necessitates accurate identification of genetic mutations.

Purpose of the Study:

  • To evaluate the role of liquid biopsy in the selection and monitoring of TKI-based targeted therapy for NSCLC.
  • To assess the utility of circulating tumor cells (CTCs), cell-free DNA (cfDNA), exosomes, and tumor-educated platelets (TEPs) as biomarkers.
  • To determine if liquid biopsy can complement traditional tissue biopsy in guiding NSCLC treatment.

Main Methods:

  • Analysis of liquid biopsy elements including CTCs, cfDNA, exosomes, and TEPs.
  • Molecular analysis using digital PCR (dPCR), next-generation sequencing (NGS), and shallow whole-genome sequencing (sWGS).
  • Comparison of liquid biopsy findings with tissue biopsy for mutation detection.

Main Results:

  • Liquid biopsy enables the detection of targetable mutations required for TKI treatment in NSCLC.
  • Analysis of cfDNA and other circulating elements can identify genetic alterations relevant to TKI therapy.
  • Liquid biopsy serves as a complementary tool to invasive tissue biopsy for treatment selection and monitoring.

Conclusions:

  • Liquid biopsy shows promise in guiding targeted therapy selection and monitoring for NSCLC patients.
  • Further prospective studies with larger patient cohorts are needed to validate these findings for clinical practice.
  • The integration of liquid biopsy into clinical workflows could enhance personalized treatment strategies for NSCLC.

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