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The correlation between the abundance of EGFR T790M mutation and osimertinib response in advanced non-small cell lung cancer

BACKGROUND: Osimertinib has been adopted as the standard therapy for T790M-mediated acquired resistance to first-line epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in patients with non-small cell lung cancer (NSCLC). The detection of EGFR T790M can be evaluated using differ...

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Autores principales: Pan, Guoqiang, Chen, Kaiyan, Yu, Xiaoqing, Sheng, Jiamin, Fan, Yun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798336/
https://www.ncbi.nlm.nih.gov/pubmed/35116599
http://dx.doi.org/10.21037/tcr-21-223
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author Pan, Guoqiang
Chen, Kaiyan
Yu, Xiaoqing
Sheng, Jiamin
Fan, Yun
author_facet Pan, Guoqiang
Chen, Kaiyan
Yu, Xiaoqing
Sheng, Jiamin
Fan, Yun
author_sort Pan, Guoqiang
collection PubMed
description BACKGROUND: Osimertinib has been adopted as the standard therapy for T790M-mediated acquired resistance to first-line epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in patients with non-small cell lung cancer (NSCLC). The detection of EGFR T790M can be evaluated using different methods. The association between baseline T790M abundance and osimertinib efficacy has not been fully determined. METHODS: A total of 144 advanced NSCLC patients positive for T790M, at the time of progression, were retrospectively enrolled in this study. The effect of abundance of T790M mutation on the efficacy of osimertinib was explored. RESULTS: Among the 144 patients receiving T790M testing, 20 (13.9%) had adopted amplification refractory mutation system (ARMS), 63 (43.8%) adopted droplet digital PCR (ddPCR), and 61 (42.4%) used next-generation sequencing (NGS). The objective response rate was 54.2%, the median progression-free survival was 12.0 months, and the overall survival was 23.0 months for the NSCLC patients treated with osimertinib. Three different technologies to assess T790M mutation (including ARMS, ddPCR, and NGS) could accurately predict the efficacy of osimertinib. There was no significant relationship between the abundance of T790M mutation and the efficacy of osimertinib. CONCLUSIONS: ARMS, ddPCR, and NGS are reliable methods to evaluate EGFR T790M mutation. Osimertinib was equally effective for NSCLC patients with various abundance of T790M mutation.
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spelling pubmed-87983362022-02-02 The correlation between the abundance of EGFR T790M mutation and osimertinib response in advanced non-small cell lung cancer Pan, Guoqiang Chen, Kaiyan Yu, Xiaoqing Sheng, Jiamin Fan, Yun Transl Cancer Res Original Article BACKGROUND: Osimertinib has been adopted as the standard therapy for T790M-mediated acquired resistance to first-line epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) in patients with non-small cell lung cancer (NSCLC). The detection of EGFR T790M can be evaluated using different methods. The association between baseline T790M abundance and osimertinib efficacy has not been fully determined. METHODS: A total of 144 advanced NSCLC patients positive for T790M, at the time of progression, were retrospectively enrolled in this study. The effect of abundance of T790M mutation on the efficacy of osimertinib was explored. RESULTS: Among the 144 patients receiving T790M testing, 20 (13.9%) had adopted amplification refractory mutation system (ARMS), 63 (43.8%) adopted droplet digital PCR (ddPCR), and 61 (42.4%) used next-generation sequencing (NGS). The objective response rate was 54.2%, the median progression-free survival was 12.0 months, and the overall survival was 23.0 months for the NSCLC patients treated with osimertinib. Three different technologies to assess T790M mutation (including ARMS, ddPCR, and NGS) could accurately predict the efficacy of osimertinib. There was no significant relationship between the abundance of T790M mutation and the efficacy of osimertinib. CONCLUSIONS: ARMS, ddPCR, and NGS are reliable methods to evaluate EGFR T790M mutation. Osimertinib was equally effective for NSCLC patients with various abundance of T790M mutation. AME Publishing Company 2021-06 /pmc/articles/PMC8798336/ /pubmed/35116599 http://dx.doi.org/10.21037/tcr-21-223 Text en 2021 Translational Cancer Research. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0/.
spellingShingle Original Article
Pan, Guoqiang
Chen, Kaiyan
Yu, Xiaoqing
Sheng, Jiamin
Fan, Yun
The correlation between the abundance of EGFR T790M mutation and osimertinib response in advanced non-small cell lung cancer
title The correlation between the abundance of EGFR T790M mutation and osimertinib response in advanced non-small cell lung cancer
title_full The correlation between the abundance of EGFR T790M mutation and osimertinib response in advanced non-small cell lung cancer
title_fullStr The correlation between the abundance of EGFR T790M mutation and osimertinib response in advanced non-small cell lung cancer
title_full_unstemmed The correlation between the abundance of EGFR T790M mutation and osimertinib response in advanced non-small cell lung cancer
title_short The correlation between the abundance of EGFR T790M mutation and osimertinib response in advanced non-small cell lung cancer
title_sort correlation between the abundance of egfr t790m mutation and osimertinib response in advanced non-small cell lung cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8798336/
https://www.ncbi.nlm.nih.gov/pubmed/35116599
http://dx.doi.org/10.21037/tcr-21-223
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