Cell-free DNA next-generation sequencing prediction of response and resistance to third-generation EGFR inhibitor Journal Article


Authors: Helman, E.; Nguyen, M.; Karlovich, C. A.; Despain, D.; Choquette, A. K.; Spira, A. I.; Yu, H. A.; Camidge, D. R.; Harding, T. C.; Lanman, R. B.; Simmons, A. D.
Article Title: Cell-free DNA next-generation sequencing prediction of response and resistance to third-generation EGFR inhibitor
Abstract: Introduction: The genomic alterations driving resistance to third-generation EGFR tyrosine kinase inhibitors (TKIs) are not well established, and collecting tissue biopsy samples poses potential complications from invasive procedures. Cell-free circulating DNA (cfDNA) testing provides a noninvasive approach to identify potentially targetable mechanisms of resistance. Here we utilized a 70-gene cfDNA next-generation sequencing test to interrogate pretreatment and progression samples from 77 EGFR-mutated non-small cell lung cancer (NSCLC) patients treated with a third-generation EGFR TKI. Patients and Methods: Rociletinib was evaluated in advanced or metastatic (second line or higher) disease with EGFR T790M-positive NSCLC in the TIGER-X (NCT01526928) and TIGER-2 (NCT02147990) studies. Plasma samples were collected at baseline and at the time of systemic progression while receiving rociletinib. The critical exons in 70 genes were sequenced in cfDNA isolated from plasma samples to elucidate a comprehensive genomic profile of alterations for each patient. Results: Plasma-based cfDNA analysis identified 93% of the initial EGFR activating and 85% of the EGFR T790M resistance mutations in pretreatment samples with detectable tumor DNA. Profiling of progression samples revealed significant heterogeneity, with different variant types (eg, mutations, amplifications, and fusions) detected in multiple genes (EGFR, MET, RB1) that may be driving resistance in patients. Novel alterations not previously described in association with resistance to third-generation TKIs were also detected, such as an NTRK1 fusion. Conclusion: cfDNA next-generation sequencing identified initial EGFR activating and secondary T790M resistance mutations in NSCLC patients with high sensitivity, predicted treatment response equivalent to tissue analysis, and identified multiple novel and established resistance alterations. We profiled 77 non–small-cell lung cancer patients with paired baseline and progression blood samples treated with the third-generation EGFR tyrosine kinase inhibitor (TKI) rociletinib using a broad cell-free circulating DNA (cfDNA) next-generation sequencing (NGS) gene panel. We demonstrated a utility of cfDNA NGS to detect EGFR T790M and predict response comparable to tissue-based tests, even at low allele fractions, and we identified resistance mechanisms. Our findings highlight the genomic heterogeneity observed in disease after progression while receiving therapy with a third-generation EGFR TKI. © 2018 The Authors
Keywords: adult; human tissue; treatment response; aged; major clinical study; allele; tumor volume; drug resistance; prediction; dna; drug response; tyrosine kinase inhibitor; plasma; non small cell lung cancer; nsclc; clinical outcome; next generation sequencing; mapk signaling; human; male; female; article; egfr t790m; circulating tumor dna; rociletinib; x-ray computed tomography; ntrk fusion; ctdna gene panel; ctdna sequencing; egfr c797s; third-generation tki; cell free nucleic acid
Journal Title: Clinical Lung Cancer
Volume: 19
Issue: 6
ISSN: 1525-7304
Publisher: Elsevier Inc.  
Date Published: 2018-11-01
Start Page: 518
End Page: 530.e7
Language: English
DOI: 10.1016/j.cllc.2018.07.008
PUBMED: 30279111
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 3 December 2018 -- Source: Scopus
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  1. Helena Alexandra Yu
    104 Yu