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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601690/ https://www.ncbi.nlm.nih.gov/pubmed/32998450 http://dx.doi.org/10.3390/diagnostics10100765 |
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author | Cortiula, Francesco Pasello, Giulia Follador, Alessandro Nardo, Giorgia Polo, Valentina Scquizzato, Elisa Conte, Alessandro Del Miorin, Marta Giovanis, Petros D’Urso, Alessandra Girlando, Salvator Settanni, Giulio Picece, Vincenzo Veccia, Antonello Corvaja, Carla Indraccolo, Stefano De Maglio, Giovanna |
author_facet | Cortiula, Francesco Pasello, Giulia Follador, Alessandro Nardo, Giorgia Polo, Valentina Scquizzato, Elisa Conte, Alessandro Del Miorin, Marta Giovanis, Petros D’Urso, Alessandra Girlando, Salvator Settanni, Giulio Picece, Vincenzo Veccia, Antonello Corvaja, Carla Indraccolo, Stefano De Maglio, Giovanna |
author_sort | Cortiula, Francesco |
collection | PubMed |
description | 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%). |
format | Online Article Text |
id | pubmed-7601690 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-76016902020-11-01 A Multi-Center, Real-Life Experience on Liquid Biopsy Practice for EGFR Testing in Non-Small Cell Lung Cancer (NSCLC) Patients Cortiula, Francesco Pasello, Giulia Follador, Alessandro Nardo, Giorgia Polo, Valentina Scquizzato, Elisa Conte, Alessandro Del Miorin, Marta Giovanis, Petros D’Urso, Alessandra Girlando, Salvator Settanni, Giulio Picece, Vincenzo Veccia, Antonello Corvaja, Carla Indraccolo, Stefano De Maglio, Giovanna Diagnostics (Basel) Article 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%). MDPI 2020-09-28 /pmc/articles/PMC7601690/ /pubmed/32998450 http://dx.doi.org/10.3390/diagnostics10100765 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Cortiula, Francesco Pasello, Giulia Follador, Alessandro Nardo, Giorgia Polo, Valentina Scquizzato, Elisa Conte, Alessandro Del Miorin, Marta Giovanis, Petros D’Urso, Alessandra Girlando, Salvator Settanni, Giulio Picece, Vincenzo Veccia, Antonello Corvaja, Carla Indraccolo, Stefano De Maglio, Giovanna A Multi-Center, Real-Life Experience on Liquid Biopsy Practice for EGFR Testing in Non-Small Cell Lung Cancer (NSCLC) Patients |
title | A Multi-Center, Real-Life Experience on Liquid Biopsy Practice for EGFR Testing in Non-Small Cell Lung Cancer (NSCLC) Patients |
title_full | A Multi-Center, Real-Life Experience on Liquid Biopsy Practice for EGFR Testing in Non-Small Cell Lung Cancer (NSCLC) Patients |
title_fullStr | A Multi-Center, Real-Life Experience on Liquid Biopsy Practice for EGFR Testing in Non-Small Cell Lung Cancer (NSCLC) Patients |
title_full_unstemmed | A Multi-Center, Real-Life Experience on Liquid Biopsy Practice for EGFR Testing in Non-Small Cell Lung Cancer (NSCLC) Patients |
title_short | A Multi-Center, Real-Life Experience on Liquid Biopsy Practice for EGFR Testing in Non-Small Cell Lung Cancer (NSCLC) Patients |
title_sort | multi-center, real-life experience on liquid biopsy practice for egfr testing in non-small cell lung cancer (nsclc) patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7601690/ https://www.ncbi.nlm.nih.gov/pubmed/32998450 http://dx.doi.org/10.3390/diagnostics10100765 |
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