Tissue or liquid rebiopsy? A prospective study for simultaneous tissue and liquid NGS after first-line EGFR inhibitor resistance in lung cancer

Yen Ting Lin, Chao Chi Ho, Wei Hsun Hsu, Wei Yu Liao, Ching Yao Yang, Chong Jen Yu, Tzu Hsiu Tsai, James Chih Hsin Yang, Shang Gin Wu, Chia Lin Hsu, Min Shu Hsieh, Yen Lin Huang, Chia Ling Wu, Jin Yuan Shih*

*Corresponding author for this work

Research output: Contribution to journalJournal Article peer-review

1 Scopus citations

Abstract

Introduction: According to current International Association for the Study of Lung Cancer guideline, physicians may first use plasma cell-free DNA (cfDNA) methods to identify epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI)-resistant mechanisms (liquid rebiopsy) for lung cancer. Tissue rebiopsy is recommended if the plasma result is negative. However, this approach has not been evaluated prospectively using next-generation sequencing (NGS). Methods: We prospectively enrolled patients with lung cancer with first-line EGFR-TKI resistance who underwent tissue rebiopsy. The rebiopsied tissues and cfDNA were sequenced using targeted NGS, ACTDrug®+, and ACTMonitor®Lung simultaneously. The clinicopathological characteristics and treatment outcomes were analyzed. Results: Totally, 86 patients were enrolled. Twenty-six (30%) underwent tissue biopsy but the specimens were inadequate for NGS. Among the 60 patients with paired tissue and liquid rebiopsies, two-thirds (40/60) may still be targetable. T790M mutations were found in 29, including 14 (48%) only from tissue and 5 (17%) only from cfDNA. Twenty-four of them were treated with osimertinib, and progression-free survival was longer in patients without detectable T790M in cfDNA than in patients with detectable T790M in cfDNA (p = 0.02). For the 31 T790M-negative patients, there were six with mesenchymal–epithelial transition factor (MET) amplifications, four with ERBB2 amplifications, and one with CCDC6-RET fusion. One with MET amplification and one with ERBB2 amplification responded to subsequent MET and ERBB2 targeting agents respectively. Conclusions: NGS after EGFR-TKI resistance may detect targetable drivers besides T790M. To do either liquid or tissue NGS only could miss patients with T790M. To do tissue and liquid NGS in parallel after EGFR-TKI resistance may find more patients with targetable cancers.

Original languageEnglish
Article numbere6870
Pages (from-to)e6870
JournalCancer Medicine
Volume13
Issue number1
DOIs
StatePublished - 01 2024
Externally publishedYes

Bibliographical note

© 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

Keywords

  • EGFR mutation
  • EGFR-TKI resistance
  • next-generation sequencing
  • NSCLC
  • Prospective Studies
  • Humans
  • Middle Aged
  • Male
  • Cell-Free Nucleic Acids/genetics
  • Biomarkers, Tumor/genetics
  • High-Throughput Nucleotide Sequencing/methods
  • ErbB Receptors/genetics
  • Liquid Biopsy/methods
  • Biopsy
  • Lung Neoplasms/drug therapy
  • Drug Resistance, Neoplasm/genetics
  • Protein Kinase Inhibitors/therapeutic use
  • Carcinoma, Non-Small-Cell Lung/drug therapy
  • Aged, 80 and over
  • Female
  • Adult
  • Aged
  • Mutation

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