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Updated: Feb 10, 2026

Exosomal miRNA Analysis in Non-small Cell Lung Cancer NSCLC Patients' Plasma Through qPCR: A Feasible Liquid Biopsy Tool
Published on: May 27, 2016
Feasibility of re-biopsy and EGFR mutation analysis in patients with non-small cell lung cancer
Tae-Ok Kim1, In-Jae Oh1,2, Bo Gun Kho1
1Department of Internal Medicine, Chonnam National University Medical School, Gwangju, South Korea.
Background:
In cases of EGFR-tyrosine kinase inhibitor (TKI) failure, re-biopsy may be useful to understand resistance mechanisms and guide further treatment decisions. However, performing re-biopsy is challenging because of several hurdles. We assessed the feasibility of re-biopsy in advanced non-small cell lung cancer (NSCLC) patients in real-world clinical practice.
Methods:
We retrospectively reviewed the clinical and pathologic data of advanced NSCLC patients who experienced disease progression after previous treatment with EGFR-TKIs at a single tertiary hospital in Korea between January 2014 and December 2016. Re-biopsy specimens included small biopsy, surgical tissue, or liquid-based cytology. EGFR mutation was tested using peptide nucleic acid-mediated clamping PCR.
Results:
Of the 230 NSCLC patients that experienced progression after EGFR-TKI therapy, 105 (45.7%) underwent re-biopsy. Re-biopsy was successfully performed in 94 (89.5%) patients, and 11 patients were diagnosed with no malignancy. The complication rate was 8.6%, including seven cases of pneumothorax. EGFR mutation testing was performed on 75 patients using re-biopsy specimens. Of the 57 patients who had sensitizing mutations at diagnosis, T790M mutations were found in 19 (33.3%), while 38 (66.7%) had no T790M mutation. Multivariate analysis showed that the re-biopsy group was younger (P = 0.002) and exhibited a previous response to EGFR-TKIs (P < 0.001).
Conclusion:
Re-biopsy in advanced NSCLC is feasible in real world clinical practice, particularly in younger patients and those who achieved a previous response to EGFR-TKIs.
Insights
Re-biopsy is feasible in advanced non-small cell lung cancer (NSCLC) patients after EGFR-TKI failure. This procedure is particularly successful in younger patients and those who previously responded to EGFR-TKIs, aiding treatment decisions.
Area of Science:
- Oncology
- Medical Diagnostics
Background:
- EGFR-tyrosine kinase inhibitor (TKI) resistance necessitates understanding mechanisms for treatment guidance.
- Re-biopsy is a potential method to identify resistance but faces practical challenges.
Purpose of the Study:
- To assess the feasibility of re-biopsy in advanced non-small cell lung cancer (NSCLC) patients post-EGFR-TKI failure in real-world clinical settings.
Main Methods:
- Retrospective review of advanced NSCLC patients treated with EGFR-TKIs between 2014-2016.
- Analysis of re-biopsy success rates, complications, and EGFR mutation status (T790M) from various specimen types.
- Multivariate analysis to identify factors associated with successful re-biopsy.
Main Results:
- Re-biopsy was performed in 45.7% of eligible patients, with a success rate of 89.5%.
- Complication rate was 8.6%, with pneumothorax being the most common.
- T790M mutations were identified in 33.3% of patients with prior sensitizing mutations.
Conclusions:
- Re-biopsy is a feasible strategy in advanced NSCLC patients experiencing EGFR-TKI failure.
- Younger patients and those with a prior positive response to EGFR-TKIs were more likely to undergo successful re-biopsy.
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