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Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study
Background: We developed a hybrid platform using a negative combined with a positive selection strategy to capture circulating tumor cells (CTCs) and detect epidermal growth factor receptor (EGFR) mutations in patients with metastatic lung adenocarcinoma. Methods: Blood samples were collected from p...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9505961/ https://www.ncbi.nlm.nih.gov/pubmed/36142574 http://dx.doi.org/10.3390/ijms231810661 |
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author | Li, Shih-Hong Wu, Min-Hsien Wang, Hung-Ming Hsu, Ping-Chih Fang, Yueh-Fu Wang, Chih-Liang Chu, Hui-Chun Lin, Hung-Chih Lee, Li-Yu Wu, Ching-Yang Yang, Cheng-Ta Chen, Jen-Shi Hsieh, Jason Chia-Hsun |
author_facet | Li, Shih-Hong Wu, Min-Hsien Wang, Hung-Ming Hsu, Ping-Chih Fang, Yueh-Fu Wang, Chih-Liang Chu, Hui-Chun Lin, Hung-Chih Lee, Li-Yu Wu, Ching-Yang Yang, Cheng-Ta Chen, Jen-Shi Hsieh, Jason Chia-Hsun |
author_sort | Li, Shih-Hong |
collection | PubMed |
description | Background: We developed a hybrid platform using a negative combined with a positive selection strategy to capture circulating tumor cells (CTCs) and detect epidermal growth factor receptor (EGFR) mutations in patients with metastatic lung adenocarcinoma. Methods: Blood samples were collected from patients with pathology-proven treatment-naïve stage IV lung adenocarcinoma. Genomic DNA was extracted from CTCs collected for EGFR mutational tests. The second set of CTC-EGFR mutational tests were performed after three months of anti-cancer therapy. Results: A total of 80 samples collected from 28 patients enrolled between July 2016 and August 2018. Seventeen patients had EGFR mutations, including Exon 19 deletion (n = 11), L858R (n = 5), and de-novo T790 and L858R (n = 1). Concordance between tissue and CTCs before treatment was 88.2% in EGFR- mutant patients and 90.9% in non-mutant patients. The accuracy, sensitivity, specificity, positive predictive value, and negative predictive value of EGFR mutation tests for CTCs were 89.3%, 88.2%, 90.9%, 93.8%, and 83.3%, respectively. Conclusions: CTCs captured by a hybrid platform using a negative and positive selection strategy may serve as a suitable and reliable source of lung cancer tumor DNA for detecting EGFR mutations, including T790M. |
format | Online Article Text |
id | pubmed-9505961 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-95059612022-09-24 Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study Li, Shih-Hong Wu, Min-Hsien Wang, Hung-Ming Hsu, Ping-Chih Fang, Yueh-Fu Wang, Chih-Liang Chu, Hui-Chun Lin, Hung-Chih Lee, Li-Yu Wu, Ching-Yang Yang, Cheng-Ta Chen, Jen-Shi Hsieh, Jason Chia-Hsun Int J Mol Sci Article Background: We developed a hybrid platform using a negative combined with a positive selection strategy to capture circulating tumor cells (CTCs) and detect epidermal growth factor receptor (EGFR) mutations in patients with metastatic lung adenocarcinoma. Methods: Blood samples were collected from patients with pathology-proven treatment-naïve stage IV lung adenocarcinoma. Genomic DNA was extracted from CTCs collected for EGFR mutational tests. The second set of CTC-EGFR mutational tests were performed after three months of anti-cancer therapy. Results: A total of 80 samples collected from 28 patients enrolled between July 2016 and August 2018. Seventeen patients had EGFR mutations, including Exon 19 deletion (n = 11), L858R (n = 5), and de-novo T790 and L858R (n = 1). Concordance between tissue and CTCs before treatment was 88.2% in EGFR- mutant patients and 90.9% in non-mutant patients. The accuracy, sensitivity, specificity, positive predictive value, and negative predictive value of EGFR mutation tests for CTCs were 89.3%, 88.2%, 90.9%, 93.8%, and 83.3%, respectively. Conclusions: CTCs captured by a hybrid platform using a negative and positive selection strategy may serve as a suitable and reliable source of lung cancer tumor DNA for detecting EGFR mutations, including T790M. MDPI 2022-09-13 /pmc/articles/PMC9505961/ /pubmed/36142574 http://dx.doi.org/10.3390/ijms231810661 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Li, Shih-Hong Wu, Min-Hsien Wang, Hung-Ming Hsu, Ping-Chih Fang, Yueh-Fu Wang, Chih-Liang Chu, Hui-Chun Lin, Hung-Chih Lee, Li-Yu Wu, Ching-Yang Yang, Cheng-Ta Chen, Jen-Shi Hsieh, Jason Chia-Hsun Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study |
title | Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study |
title_full | Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study |
title_fullStr | Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study |
title_full_unstemmed | Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study |
title_short | Circulating EGFR Mutations in Patients with Lung Adenocarcinoma by Circulating Tumor Cell Isolation Systems: A Concordance Study |
title_sort | circulating egfr mutations in patients with lung adenocarcinoma by circulating tumor cell isolation systems: a concordance study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9505961/ https://www.ncbi.nlm.nih.gov/pubmed/36142574 http://dx.doi.org/10.3390/ijms231810661 |
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