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Analysis of resistance mechanisms to abivertinib, a third-generation EGFR tyrosine kinase inhibitor, in patients with EGFR T790M-positive non-small cell lung cancer from a phase I trial

BACKGROUND: Resistance to third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) presents a major clinical challenge in advanced non-small cell lung cancer (NSCLC). Here, we report resistance mechanisms to abivertinib, a novel third-generation EGFR TKI, from a pha...

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Autores principales: Zhang, Yi-Chen, Chen, Zhi-Hong, Zhang, Xu-Chao, Xu, Chong-Rui, Yan, Hong-Hong, Xie, Zhi, Chuai, Shao-Kun, Ye, Jun-Yi, Han-Zhang, Han, Zhang, Zhou, Bai, Xiao-Yan, Su, Jian, Gan, Bin, Yang, Jin-Ji, Li, Wen-Feng, Tang, Wei, Luo, Feng Roger, Xu, Xiao, Wu, Yi-Long, Zhou, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558024/
https://www.ncbi.nlm.nih.gov/pubmed/31027916
http://dx.doi.org/10.1016/j.ebiom.2019.04.030
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author Zhang, Yi-Chen
Chen, Zhi-Hong
Zhang, Xu-Chao
Xu, Chong-Rui
Yan, Hong-Hong
Xie, Zhi
Chuai, Shao-Kun
Ye, Jun-Yi
Han-Zhang, Han
Zhang, Zhou
Bai, Xiao-Yan
Su, Jian
Gan, Bin
Yang, Jin-Ji
Li, Wen-Feng
Tang, Wei
Luo, Feng Roger
Xu, Xiao
Wu, Yi-Long
Zhou, Qing
author_facet Zhang, Yi-Chen
Chen, Zhi-Hong
Zhang, Xu-Chao
Xu, Chong-Rui
Yan, Hong-Hong
Xie, Zhi
Chuai, Shao-Kun
Ye, Jun-Yi
Han-Zhang, Han
Zhang, Zhou
Bai, Xiao-Yan
Su, Jian
Gan, Bin
Yang, Jin-Ji
Li, Wen-Feng
Tang, Wei
Luo, Feng Roger
Xu, Xiao
Wu, Yi-Long
Zhou, Qing
author_sort Zhang, Yi-Chen
collection PubMed
description BACKGROUND: Resistance to third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) presents a major clinical challenge in advanced non-small cell lung cancer (NSCLC). Here, we report resistance mechanisms to abivertinib, a novel third-generation EGFR TKI, from a phase I dose-escalation/expansion study (NCT02330367). METHODS: Patients with EGFR T790M-positive advanced NSCLC and progression on prior EGFR TKIs received abivertinib in dose escalation (50–350 mg twice daily [BID]) or expansion (300 mg BID) cohorts. Patients enrolled at Guangdong Lung Cancer Institute who underwent next-generation sequencing (NGS)-based genomic profiling upon abivertinib progression (prior to October 30, 2018) were enrolled in this exploratory analysis. FINDINGS: Thirty of 73 patients enrolled were eligible for resistance analysis. Upon abivertinib progression, 27 patients provided plasma samples (six patients also provided paired samples from the progression sites) and three patients only provided tissue samples from the progression sites for NGS. A heterogeneous landscape of resistance to abivertinib was observed: 15% (4/27) experienced EGFR T790M loss and 13% (4/30) developing EGFR tertiary mutations including C797S. EGFR amplification was observed in 11 patients (37%), and considered a putative resistance mechanism in seven (23%) patients. Other EGFR-independent resistance mechanisms involved CDKN2A, MET, PIK3CA, HER2, TP53, Rb1 and small-cell lung cancer transformation. INTERPRETATION: Our findings reveal a heterogenous pattern of resistance mechanisms to abivertinib which is distinct from that previously reported with osimertinib. EGFR amplification was the most common resistance mechanism in this cohort. FUND: The National Key R&D Program of China (Grant No. 2016YFC1303800), Key Lab System Project of Guangdong Science and Technology Department – Guangdong Provincial Key Lab of Translational Medicine in Lung Cancer (Grant No. 2012A061400006/2017B030314120).
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spelling pubmed-65580242019-06-14 Analysis of resistance mechanisms to abivertinib, a third-generation EGFR tyrosine kinase inhibitor, in patients with EGFR T790M-positive non-small cell lung cancer from a phase I trial Zhang, Yi-Chen Chen, Zhi-Hong Zhang, Xu-Chao Xu, Chong-Rui Yan, Hong-Hong Xie, Zhi Chuai, Shao-Kun Ye, Jun-Yi Han-Zhang, Han Zhang, Zhou Bai, Xiao-Yan Su, Jian Gan, Bin Yang, Jin-Ji Li, Wen-Feng Tang, Wei Luo, Feng Roger Xu, Xiao Wu, Yi-Long Zhou, Qing EBioMedicine Research paper BACKGROUND: Resistance to third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) presents a major clinical challenge in advanced non-small cell lung cancer (NSCLC). Here, we report resistance mechanisms to abivertinib, a novel third-generation EGFR TKI, from a phase I dose-escalation/expansion study (NCT02330367). METHODS: Patients with EGFR T790M-positive advanced NSCLC and progression on prior EGFR TKIs received abivertinib in dose escalation (50–350 mg twice daily [BID]) or expansion (300 mg BID) cohorts. Patients enrolled at Guangdong Lung Cancer Institute who underwent next-generation sequencing (NGS)-based genomic profiling upon abivertinib progression (prior to October 30, 2018) were enrolled in this exploratory analysis. FINDINGS: Thirty of 73 patients enrolled were eligible for resistance analysis. Upon abivertinib progression, 27 patients provided plasma samples (six patients also provided paired samples from the progression sites) and three patients only provided tissue samples from the progression sites for NGS. A heterogeneous landscape of resistance to abivertinib was observed: 15% (4/27) experienced EGFR T790M loss and 13% (4/30) developing EGFR tertiary mutations including C797S. EGFR amplification was observed in 11 patients (37%), and considered a putative resistance mechanism in seven (23%) patients. Other EGFR-independent resistance mechanisms involved CDKN2A, MET, PIK3CA, HER2, TP53, Rb1 and small-cell lung cancer transformation. INTERPRETATION: Our findings reveal a heterogenous pattern of resistance mechanisms to abivertinib which is distinct from that previously reported with osimertinib. EGFR amplification was the most common resistance mechanism in this cohort. FUND: The National Key R&D Program of China (Grant No. 2016YFC1303800), Key Lab System Project of Guangdong Science and Technology Department – Guangdong Provincial Key Lab of Translational Medicine in Lung Cancer (Grant No. 2012A061400006/2017B030314120). Elsevier 2019-04-23 /pmc/articles/PMC6558024/ /pubmed/31027916 http://dx.doi.org/10.1016/j.ebiom.2019.04.030 Text en © 2019 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research paper
Zhang, Yi-Chen
Chen, Zhi-Hong
Zhang, Xu-Chao
Xu, Chong-Rui
Yan, Hong-Hong
Xie, Zhi
Chuai, Shao-Kun
Ye, Jun-Yi
Han-Zhang, Han
Zhang, Zhou
Bai, Xiao-Yan
Su, Jian
Gan, Bin
Yang, Jin-Ji
Li, Wen-Feng
Tang, Wei
Luo, Feng Roger
Xu, Xiao
Wu, Yi-Long
Zhou, Qing
Analysis of resistance mechanisms to abivertinib, a third-generation EGFR tyrosine kinase inhibitor, in patients with EGFR T790M-positive non-small cell lung cancer from a phase I trial
title Analysis of resistance mechanisms to abivertinib, a third-generation EGFR tyrosine kinase inhibitor, in patients with EGFR T790M-positive non-small cell lung cancer from a phase I trial
title_full Analysis of resistance mechanisms to abivertinib, a third-generation EGFR tyrosine kinase inhibitor, in patients with EGFR T790M-positive non-small cell lung cancer from a phase I trial
title_fullStr Analysis of resistance mechanisms to abivertinib, a third-generation EGFR tyrosine kinase inhibitor, in patients with EGFR T790M-positive non-small cell lung cancer from a phase I trial
title_full_unstemmed Analysis of resistance mechanisms to abivertinib, a third-generation EGFR tyrosine kinase inhibitor, in patients with EGFR T790M-positive non-small cell lung cancer from a phase I trial
title_short Analysis of resistance mechanisms to abivertinib, a third-generation EGFR tyrosine kinase inhibitor, in patients with EGFR T790M-positive non-small cell lung cancer from a phase I trial
title_sort analysis of resistance mechanisms to abivertinib, a third-generation egfr tyrosine kinase inhibitor, in patients with egfr t790m-positive non-small cell lung cancer from a phase i trial
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6558024/
https://www.ncbi.nlm.nih.gov/pubmed/31027916
http://dx.doi.org/10.1016/j.ebiom.2019.04.030
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