Literature DB >> 31027703

The presence and variant allele fraction of EGFR mutations in ctDNA and development of resistance.

Grainne M O'Kane1, Geoffrey Liu1, Tracy L Stockley1, Muqdas Shabir1, Tong Zhang1, Jennifer H Law1, Lisa W Le1, Adrian Sacher1, Frances A Shepherd1, Penelope A Bradbury1, Natasha B Leighl2.   

Abstract

BACKGROUND: Peripheral blood sampling for detection of EGFR T790M in cell-free circulating tumour (ct) DNA in TKI-resistant EGFR mutant (EGFRm) lung cancer is now standard. The value of more comprehensive sequencing is unknown.
METHODS: Prospective ctDNA analysis in patients with EGFRm NSCLC was performed using a next generation sequencing (NGS) panel of regions of 11 genes detecting single nucleotide variants and small insertions/deletions at ≥0.1% variant allele frequency (VAF) was performed. Patients were grouped according to treatment phase, including: (A) pre EGFR-TKI, (B) stable or responding to EGFR-TKI, (C) radiographic progression during EGFR-TKI, and (D) during chemotherapy treatment.
RESULTS: Seventy-two patients with stage IV EGFRm NSCLC were enrolled and first blood samples were analysed. Primary sensitizing mutations in del19 or L858R were present in 66 (92%) and uncommon EGFRm in 6 (8%). Mutations in ctDNA were found in 53 samples (74%). T790M was detected in 3 of 4 patients with T790M-negative tissue. Other co-occurring EGFRm were found in 10 patients (7%) including K745R during first-line osimertinib. TP53 (n = 10), KRAS (n = 1), PI3KCA (n = 1) and ALK (n = 3) gene mutations also were detected. The presence of an EGFRm (excluding T790M) was associated with untreated or progressive disease, p = 0.04. In TKI-treated patients without radiologic progression, median progression free survival (PFS) was 10 months versus 2.1 months (HR 2.22, 95% CI: 0.89-5.54, p = 0.08) if an EGFRm in ctDNA was detected. If T790M was present in ctDNA, median PFS was 3.0 months versus 9.7 months (HR 4.59, 95% CI: 1.43-14.73, p = 0.005). High % VAF of both EGFRm and T790M correlated with inferior PFS (p = 0.01 and p = 0.03 respectively).
CONCLUSION: In addition to the emergence of resistance mutations, the presence of the primary or co-occurring EGFRm in patients receiving EGFR-TKIs may associate with shorter PFS and may be useful in longitudinal analyses of ctDNA to direct therapy.
Copyright © 2019 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  EGFR mutation; Non-small cell lung cancer; Resistance; Variant allelic fraction

Mesh:

Substances:

Year:  2019        PMID: 31027703     DOI: 10.1016/j.lungcan.2019.03.019

Source DB:  PubMed          Journal:  Lung Cancer        ISSN: 0169-5002            Impact factor:   5.705


  5 in total

1.  Molecular pathology testing for non-small cell lung cancer: an observational study of elements currently present in request forms and result reports and the opinion of different stakeholders.

Authors:  Kelly Dufraing; Kaat Van Casteren; Joke Breyne; Nicky D'Haene; Claude Van Campenhout; Sara Vander Borght; Karen Zwaenepoel; Etienne Rouleau; Ed Schuuring; Jan von der Thüsen; Elisabeth Dequeker
Journal:  BMC Cancer       Date:  2022-07-06       Impact factor: 4.638

2.  Gene alternation of cerebrospinal fluid in patients with leptomeningeal metastases of lung adenocarcinoma using next-generation sequencing.

Authors:  Hainan Yang; Lei Wen; Yingying Pan; Changguo Shan; Weiping Hong; Hui Wang; Cheng Zhou; Linbo Cai; Caicun Zhou
Journal:  BMC Cancer       Date:  2022-05-25       Impact factor: 4.638

Review 3.  The Validity and Predictive Value of Blood-Based Biomarkers in Prediction of Response in the Treatment of Metastatic Non-Small Cell Lung Cancer: A Systematic Review.

Authors:  Frederik van Delft; Hendrik Koffijberg; Valesca Retèl; Michel van den Heuvel; Maarten IJzerman
Journal:  Cancers (Basel)       Date:  2020-04-30       Impact factor: 6.639

4.  Clinical Outcomes in Non-Small-Cell Lung Cancer Patients Treated With EGFR-Tyrosine Kinase Inhibitors and Other Targeted Therapies Based on Tumor Versus Plasma Genomic Profiling.

Authors:  Hai T Tran; Vincent K Lam; Yasir Y Elamin; Lingzhi Hong; Rivka Colen; Nabil A Elshafeey; Islam S A Hassan; Mehmet Altan; George R Blumenschein; Waree Rinsurongkawong; Melvin J Rivera; Mayra E Vasquez; Brett W Carter; Lauren E Byers; Anne S Tsao; Don L Gibbons; Frank Fossella; Bonnie S Glisson; Jianjun Zhang; John V Heymach
Journal:  JCO Precis Oncol       Date:  2021-08-05

5.  Preoperative detection of KRAS G12D mutation in ctDNA is a powerful predictor for early recurrence of resectable PDAC patients.

Authors:  Shiwei Guo; Xiaohan Shi; Jing Shen; Suizhi Gao; Huan Wang; Shuo Shen; Yaqi Pan; Bo Li; Xiongfei Xu; Zhuo Shao; Gang Jin
Journal:  Br J Cancer       Date:  2020-01-23       Impact factor: 7.640

  5 in total

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