Potential Therapeutic Strategy for EGFR-Mutant Lung Cancer With Concomitant EML4-ALK Rearrangement-Combination of EGFR Tyrosine Kinase Inhibitors and ALK Inhibitors

被引:9
作者
Huang, Ming-Hung [1 ]
Lee, Jih-Hsiang [1 ,2 ]
Hung, Pei-Shan [1 ]
Yang, James Chih-Hsin [1 ,2 ,3 ,4 ]
机构
[1] Natl Taiwan Univ, Grad Inst Oncol, Coll Med, Taipei, Taiwan
[2] Natl Taiwan Univ Hosp, Dept Oncol, Taipei, Taiwan
[3] Natl Taiwan Univ, Grad Inst Oncol, 7 Chung Shan South Rd, Taipei 100, Taiwan
[4] Natl Taiwan Univ, Canc Res Ctr, 7 Chung Shan South Rd, Taipei 100, Taiwan
关键词
EGFR; EML4-ALK; Lung cancer; EGFR-TKI; ALK inhibitor; ACQUIRED-RESISTANCE; DRIVER MUTATIONS; FUSION GENE; OSIMERTINIB; ADENOCARCINOMA; TRANSLOCATION; MECHANISMS; OUTCOMES; TKI;
D O I
10.1016/j.jtocrr.2022.100405
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Although driver gene mutations have been believed to be mutually exclusive, some patients with NSCLC and concomitant EGFR mutations and EML4-ALK rearrangements have been reported. In this study, we reported a case of a patient with lung cancer who harbored both EGFR mutation and the EML4-ALK rearrangement after acquiring resistance to the EGFR tyrosine kinase inhibitor treatment. EGFR-mutant and ALK fusion proteins were detected in the same tumor cells through immunohistochemical analysis. Investigation of the molecular mechanisms of concomitant EGFR mutation and the EML4-ALK rearrangement in the same tumor cell can help discover an appropriate treatment for these patients. Methods: PC-9 cells, expressing EGFR exon 19 deletion, were transfected with EML4-ALK variant 3a (v3a) and variant 3b (v3b) separately and selected, and the effect of EGFR and ALK inhibitors was evaluated in vitro and in vivo. Results: PC-9_v3a-gef and PC-9_v3b-gef cells were resistant to gefitinib and ALK inhibitors alone, but ALK inhibitors enhanced gefitinib-induced cytotoxicity. In animal studies, gefitinib completely inhibited the tumor growth in PC-9_vector cells but not in PC-9_v3a-gef and PC-9_v3b-gef cells. A combination of ALK inhibitor and gefitinib was found to be more potent than gefitinib alone in PC-9_v3a-gef and PC-9_v3b-gef cells. Furthermore, combination treatment with osimertinib and ceritinib caused a decrease in liver tumor size of the patient with liver metastases. Conclusions: Our data suggest that combination treatment with EGFR and ALK inhibitors can be a therapeutic strategy for treating NSCLC with concomitant EGFR mutation and EML4-ALK rearrangement. (C) 2022 The Authors. Published by Elsevier Inc. on behalf of the International Association for the Study of Lung Cancer. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
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页数:13
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