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Cited by 448Lung Cancer Treatments and MutationsCancer Genomics and DiagnosticsLung Cancer Diagnosis and Treatment

The DOI matches its Crossref record; 28 of the 28 references it cites were found in a registry or an index.

Gefitinib Treatment in EGFR Mutated Caucasian NSCLC: Circulating-Free Tumor DNA as a Surrogate for Determination of EGFR Status

Open access
Douillard, Jean-Yves, Ostoros, Gyula, Cobo, Manuel, Ciuleanu, Tudor, Cole, Rebecca, McWalter, Gael, Walker, Jill, Dearden, Simon, Webster, Alan, Milenkova, Tsveta, McCormack, Rose·2014·Journal of Thoracic Oncology
DOI 10.1097/jto.0000000000000263PMC PMC4224589
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Abstract

INTRODUCTION: In the phase IV, open-label, single-arm study NCT01203917, first-line gefitinib 250 mg/d was effective and well tolerated in Caucasian patients with epidermal growth factor receptor (EGFR) mutation-positive non-small-cell lung cancer (previously published). Here, we report EGFR mutation analyses of plasma-derived, circulating-free tumor DNA. METHODS: Mandatory tumor and duplicate plasma (1 and 2) baseline samples were collected (all screened patients; n = 1060). Preplanned, exploratory analyses included EGFR mutation (and subtype) status of tumor versus plasma and between plasma samples. Post hoc, exploratory analyses included efficacy by tumor and plasma EGFR mutation (and subtype) status. RESULTS: Available baseline tumor samples were 1033 of 1060 (118 positive of 859 mutation status known; mutation frequency, 13.7%). Available plasma 1 samples were 803 of 1060 (82 positive of 784 mutation status known; mutation frequency, 10.5%). Mutation status concordance between 652 matched tumor and plasma 1 samples was 94.3% (95% confidence interval [CI], 92.3-96.0) (comparable for mutation subtypes); test sensitivity was 65.7% (95% CI, 55.8-74.7); and test specificity was 99.8% (95% CI, 99.0-100.0). Twelve patients of unknown tumor mutation status were subsequently identified as plasma mutation-positive. Available plasma 2 samples were 803 of 1060 (65 positive of 224 mutation status-evaluable and -known). Mutation status concordance between 224 matched duplicate plasma 1 and 2 samples was 96.9% (95% CI, 93.7-98.7). Objective response rates are as follows: mutation-positive tumor, 70% (95% CI, 60.5-77.7); mutation-positive tumor and plasma 1, 76.9% (95% CI, 65.4-85.5); and mutation-positive tumor and mutation-negative plasma 1, 59.5% (95% CI, 43.5-73.7). Median progression-free survival (months) was 9.7 (95% CI, 8.5-11.0; 61 events) for mutation-positive tumor and 10.2 (95% CI, 8.5-12.5; 36 events) for mutation-positive tumor and plasma 1. CONCLUSION: The high concordance, specificity, and sensitivity demonstrate that EGFR mutation status can be accurately assessed using circulating-free tumor DNA. Although encouraging and suggesting that plasma is a suitable substitute for mutation analysis, tumor tissue should remain the preferred sample type when available.

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Research works printed but not linked: 2

  1. Reck, 2013, Investigating the utility of plasma-derived circulating-free DNA for the detection of EGFR mutations in European and Japanese patients with advanced NSCLC: ASSESS study design, J Thorac Oncol, S483
  2. Han, 2013, A diagnostic study to determine the prevalence of EGFR mutations in Asian and Russian patients with NSCLC of adenocarcinoma and non-adenocarcinoma histology: IGNITE study design, J Thorac Oncol, 8, S1098

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Metadata

Authors
Douillard, J.-Y., Ostoros, G., Cobo, M., Ciuleanu, T., Cole, R., McWalter, G., Walker, J., Dearden, S., Webster, A., Milenkova, T., & McCormack, R.
Affiliations
  • Iuliu Hațieganu University of Medicine and Pharmacy (RO)
  • Országos Korányi Tbc és Pulmonológiai Intézet (HU)
  • Hospital Regional Universitario de Málaga (ES)
  • AstraZeneca (United Kingdom) (GB)
Corresponding author
Douillard, Jean-Yves
ORCID
Venue
Journal of Thoracic Oncology
Publisher
Elsevier BV
Published
2014-09
Volume
9
Issue
9
Pages
1345-1353
ISSN
1556-0864 (ISSN-L)
DOI
10.1097/jto.0000000000000263
PMC
PMC4224589
OpenAlex
W1978285367
Cited by
448
References
28
Citations by year
2026: 2 · 2025: 7 · 2024: 8 · 2023: 16 · 2022: 20 · 2021: 37 · 2020: 44 · 2019: 69 · 2018: 70 · 2017: 72 · 2016: 63 · 2015: 38 · 2014: 2
FWCI
46.71
Type
journal article
Language
en
Open access
Licence
Locations
  • Journal of Thoracic Oncology (publishedVersion, cc-by-nc-nd)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
AstraZeneca
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Treatments and Mutations
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Cancer Genomics and Diagnostics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Diagnosis and Treatment
Keywords
gefitinib, EGFR mutation, non-small cell lung cancer, circulating tumor DNA, liquid biopsy, plasma DNA, tumor mutation status, treatment response, sensitivity and specificity, first-line therapy, Caucasian patients, EGFR tyrosine kinase inhibitors, objective response rate, progression-free survival, overall survival
MeSH terms
Gefitinib, Adult, Aged, Aged, 80 and over, Carcinoma, Non-Small-Cell Lung, DNA Mutational Analysis, DNA, Neoplasm, Female, Follow-Up Studies, Humans, Lung Neoplasms, Male, Middle Aged, Mutation, Prospective Studies, Quinazolines, Single-Blind Method, Treatment Outcome, Disease-Free Survival, Protein Kinase Inhibitors, ErbB Receptors

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