Abstract

With advances in targeted and personalized treatment for lung cancer, molecular analysis of tumors is routinely performed for sequencing of treatment options in patients with advanced non-small-cell lung cancer (NSCLC). Oncogene addiction due to driver mutations includes EGFR exon 20 insertion mutations, MET amplification, EML4-AL, KRAS G12C point mutations, RET rearrangements, HER2 amplification and mutations, and FGFR amplification and translocations. A re-biopsy at the time of tumor recurrence or progression after first-line treatment failure is important for further molecular assessment and personalized therapy. However, repeat tumor biopsies are fraught with challenges including access to the tumor, sample inadequacy, patient consent, patient performance status, safety, or physician’s choice or assessment. Cytological specimens are gaining importance but are limited due to validation difficulties. Liquid biopsies, which are minimally invasive have shown promise to assess dynamic biomarkers using ctDNA analysis and are thus frequently considered in routine clinical practice in advanced NSCLC patients to guide further targeted treatment. Here we present a comprehensive review that emphasizes the significance of performing tumor re-biopsy in advanced stage NSCLC patients following resistance to first-line treatment and simultaneously highlights the current challenges in performing the same and the current status and future perspectives of liquid biopsy in NSCLC.

Highlights

  • Lung cancer has the highest mortality rate in men and the second highest in women [1]

  • With advances in targeted and personalized treatment for lung cancer, molecular analysis of tumors is routinely performed for sequencing of treatment options in patients with advanced non-small-cell lung cancer (NSCLC)

  • We present a comprehensive review that emphasizes the significance of performing tumor re-biopsy in advanced stage NSCLC patients following resistance to first-line treatment and simultaneously highlights the current challenges in performing the same and the current status and future perspectives of liquid biopsy in NSCLC

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Summary

Introduction

Lung cancer has the highest mortality rate in men and the second highest in women [1]. The global incidence of epidermal growth factor receptor (EGFR) mutations in patients with NSCLC has been reported to be higher in the Asia-Pacific region (47%) as compared to Europe (15%) [3]. A reversible EGFR small molecule tyrosine kinase inhibitor (TKIs), in the year 2003 [4] [5], a series of targeted treatments have been introduced in the last two decades for advanced-stage NSCLC having oncogenic mutations. Over these years, several small-molecule TKIs were approved for driver mutations like ALK, ROS1, BRAF, NTRK. Other less targetable oncogenic mutations seen in NSCLC include HER2, RET, KRAS, and MET

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