A Multi-Center, Real-Life Experience on Liquid Biopsy Practice for EGFR Testing in Non-Small Cell Lung Cancer (NSCLC) Patients

Background: circulating tumor DNA (ctDNA) is a source of tumor genetic material for EGFR testing in NSCLC. Real-word data about liquid biopsy (LB) clinical practice are lacking. The aim of the study was to describe the LB practice for EGFR detection in North Eastern Italy. Methods: we conducted a mu...

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Published inDiagnostics (Basel) Vol. 10; no. 10; p. 765
Main Authors Cortiula, Francesco, Pasello, Giulia, Follador, Alessandro, Nardo, Giorgia, Polo, Valentina, Scquizzato, Elisa, Del Conte, Alessandro, Miorin, Marta, Giovanis, Petros, D’Urso, Alessandra, Girlando, Salvator, Settanni, Giulio, Picece, Vincenzo, Veccia, Antonello, Corvaja, Carla, Indraccolo, Stefano, De Maglio, Giovanna
Format Journal Article
LanguageEnglish
Published Basel MDPI AG 28.09.2020
MDPI
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Summary:Background: circulating tumor DNA (ctDNA) is a source of tumor genetic material for EGFR testing in NSCLC. Real-word data about liquid biopsy (LB) clinical practice are lacking. The aim of the study was to describe the LB practice for EGFR detection in North Eastern Italy. Methods: we conducted a multi-regional survey on ctDNA testing practices in lung cancer patients. Results: Median time from blood collection to plasma separation was 50 min (20–120 min), median time from plasma extraction to ctDNA analysis was 24 h (30 min–5 days) and median turnaround time was 24 h (6 h–5 days). Four hundred and seventy five patients and 654 samples were tested. One hundred and ninety-two patients were tested at diagnosis, with 16% EGFR mutation rate. Among the 283 patients tested at disease progression, 35% were T790M+. Main differences in LB results between 2017 and 2018 were the number of LBs performed for each patient at disease progression (2.88 vs. 1.2, respectively) and the percentage of T790M+ patients (61% vs. 26%).
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ISSN:2075-4418
2075-4418
DOI:10.3390/diagnostics10100765