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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.
Abstract:
The treatment of non-small cell lung cancer (NSCLC) has recently evolved with the introduction of targeted therapy based on the use of tyrosine kinase inhibitors (TKIs) in patients with certain gene alterations, including EGFR, ALK, ROS1, BRAF, and MET genes. Molecular targeted therapy based on TKIs has improved clinical outcomes in a large number of NSCLC patients with advanced disease, enabling significantly longer progression-free survival (PFS). Liquid biopsy is an increasingly popular diagnostic tool for treating TKI-based NSCLC. The studies presented in this article show that detection and analysis based on liquid biopsy elements such as circulating tumor cells (CTCs), cell-free DNA (cfDNA), exosomes, and/or tumor-educated platelets (TEPs) can contribute to the appropriate selection and monitoring of targeted therapy in NSCLC patients as complementary to invasive tissue biopsy. The detection of these elements, combined with their molecular analysis (using, e.g., digital PCR (dPCR), next generation sequencing (NGS), shallow whole genome sequencing (sWGS)), enables the detection of mutations, which are required for the TKI treatment. Despite such promising results obtained by many research teams, it is still necessary to carry out prospective studies on a larger group of patients in order to validate these methods before their application in clinical practice.
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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