Literature DB >> 29620164

Rapid point-of-care testing for epidermal growth factor receptor gene mutations in patients with lung cancer using cell-free DNA from cytology specimen supernatants.

Shiho Asaka1, Akihiko Yoshizawa1, Kazusa Saito2, Yukihiro Kobayashi1, Hiroshi Yamamoto3, Tatsuya Negishi1, Rie Nakata1, Kazuyuki Matsuda1, Akemi Yamaguchi4, Takayuki Honda1.   

Abstract

Epidermal growth factor receptor (EGFR) mutations are associated with responses to EGFR tyrosine kinase inhibitors (EGFR-TKIs) in non-small-cell lung cancer (NSCLC). Our previous study revealed a rapid point-of-care system for detecting EGFR mutations. This system analyzes cell pellets from cytology specimens using droplet-polymerase chain reaction (d-PCR), and has a reaction time of 10 min. The present study aimed to validate the performance of the EGFR d-PCR assay using cell-free DNA (cfDNA) from supernatants obtained from cytology specimens. Assay results from cfDNA supernatant analyses were compared with those from cell pellets for 90 patients who were clinically diagnosed with, or suspected of having, lung cancer (80 bronchial lavage fluid samples, nine pleural effusion samples and one spinal fluid sample). EGFR mutations were identified in 12 and 15 cases using cfDNA supernatants and cell pellets, respectively. The concordance rates between cfDNA-supernatant and cell‑pellet assay results were 96.7% [kappa coefficient (K)=0.87], 98.9% (K=0.94), 98.9% (K=0.79) and 98.9% (K=0.79) for total EGFR mutations, L858R, E746_A750del and T790M, respectively. All 15 patients with EGFR mutation-positive results, as determined by EGFR d-PCR assay using cfDNA supernatants or cell pellets, also displayed positive results by conventional EGFR assays using tumor tissue or cytology specimens. Notably, EGFR mutations were even detected in five cfDNA supernatants for which the cytological diagnoses of the corresponding cell pellets were 'suspicious for malignancy', 'atypical' or 'negative for malignancy.' In conclusion, this rapid point-of-care system may be considered a promising novel screening method that may enable patients with NSCLC to receive EGFR-TKI therapy more rapidly, whilst also reserving cell pellets for additional morphological and molecular analyses.

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Year:  2018        PMID: 29620164     DOI: 10.3892/ijo.2018.4334

Source DB:  PubMed          Journal:  Int J Oncol        ISSN: 1019-6439            Impact factor:   5.650


  4 in total

1.  Impact of menopausal status and HER-2/neu protein on efficacy of EGFR-TKI in EGFR mutant patients with non-small cell lung cancer.

Authors:  Zi-Jun Yin; Hai-Yan Tu; Ming Fu; Wen-Zhao Zhong; She-Juan An; Hong-Hong Yan; Hua-Jun Chen; Hui-Ran Lin; Yi-Long Wu
Journal:  J Cancer       Date:  2018-07-30       Impact factor: 4.207

2.  Cell-free DNA in the supernatant of pleural effusion can be used to detect driver and resistance mutations, and can guide tyrosine kinase inhibitor treatment decisions.

Authors:  Karlijn Hummelink; Mirte Muller; Theodora C Linders; Vincent van der Noort; Petra M Nederlof; Paul Baas; Sjaak Burgers; Egbert F Smit; Gerrit A Meijer; Michel M van den Heuvel; Daan van den Broek; Kim Monkhorst
Journal:  ERJ Open Res       Date:  2019-03-25

3.  Loop-Mediated Isothermal Amplification as Point-of-Care Testing for EGFR-Mutated Lung Adenocarcinoma.

Authors:  Yuichi Saito; Atsuka Matsui; Satoru Michiyuki; Hiroaki Morooka; Takayuki Ibi; Yoshikane Yamauchi; Nobumasa Takahashi; Yoshihiko Shimizu; Tomohiko Ikeya; Eishin Hoshi; Yukinori Sakao; Masafumi Kawamura
Journal:  Micromachines (Basel)       Date:  2022-06-06       Impact factor: 3.523

Review 4.  Testing EGFR with Idylla on Cytological Specimens of Lung Cancer: A Review.

Authors:  Alessandro Caputo; Angela D'Ardia; Francesco Sabbatino; Caterina Picariello; Chiara Ciaparrone; Pio Zeppa; Antonio D'Antonio
Journal:  Int J Mol Sci       Date:  2021-05-03       Impact factor: 5.923

  4 in total

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