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[表皮生长因子受体酪氨酸激酶抑制剂耐药继发MET基因扩增肺鳞癌1例报告并文献复习]

[A Case Report of EGFR-TKIs Resistant Secondary MET Gene Amplified 
Lung Squamous Cell Carcinoma and Literature Review].

作者信息

Liu Yalan, Chen Peng, Liu Xinfu

机构信息

Department of Oncology, The Central Hospital of Shaoyang, Shaoyang 422000, China.

Department of Thoracic Oncology, 
Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin 300060, China.

出版信息

Zhongguo Fei Ai Za Zhi. 2024 Nov 20;27(11):878-884. doi: 10.3779/j.issn.1009-3419.2024.106.32.

DOI:10.3779/j.issn.1009-3419.2024.106.32
PMID:39800484
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11732385/
Abstract

With the rapid development of epidermal growth factor receptor (EGFR) gene testing of lung adenocarcinoma patients has been routinely carried out, EGFR mutations are also possible for some small samples of non-smoking female lung squamous cell carcinoma patients. This increases the opportunity for targeted therapy for this group of patients. However, drug resistance in patients with lung squamous cell carcinoma during targeted therapy is an important factor affecting subsequent treatment. There are multiple mechanisms of acquired drug resistance in targeted therapy, and the alteration of mesenchymal-epithelial transition factor (MET) signaling pathway is one of the common mechanisms of drug resistance. At present, some selective tyrosine kinase inhibitors (TKIs) of MET has been approved for non-small cell lung cancer with MET gene 14 exon skipping mutation, such as Glumetinib, Savolitinib, Tepotinib, Capmatinib, etc. Drugs that target secondary MET amplification are still in clinical trials. This paper retrospectively analyzed the clinical data of a female patient with EGFR-TKIs resistant secondary MET amplified squamous cell lung cancer, and reviewed relevant literature to explore how to optimize the treatment of lung squamous cell carcinoma patients with EGFR mutation, so as to provide clinical reference for the diagnosis and treatment of such patients.
.

摘要

随着肺腺癌患者表皮生长因子受体(EGFR)基因检测的迅速开展并已常规进行,一些非吸烟女性肺鳞癌小样本患者也可能存在EGFR突变。这增加了该组患者接受靶向治疗的机会。然而,肺鳞癌患者在靶向治疗过程中的耐药性是影响后续治疗的重要因素。靶向治疗中获得性耐药有多种机制,间充质上皮转化因子(MET)信号通路改变是常见的耐药机制之一。目前,一些MET选择性酪氨酸激酶抑制剂(TKIs)已被批准用于治疗具有MET基因第14外显子跳跃突变的非小细胞肺癌,如谷美替尼、赛沃替尼、替泊替尼、卡马替尼等。针对继发性MET扩增的药物仍在临床试验中。本文回顾性分析了1例EGFR-TKIs耐药继发性MET扩增的肺鳞癌女性患者的临床资料,并复习相关文献,探讨如何优化EGFR突变肺鳞癌患者的治疗,为这类患者的诊治提供临床参考。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e8/11732385/e95fec109c05/zgfazz-27-11-878-img_4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e8/11732385/528cc73e058b/zgfazz-27-11-878-img_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e8/11732385/7eebce32bed3/zgfazz-27-11-878-img_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e8/11732385/f19e09f5f31b/zgfazz-27-11-878-img_3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e8/11732385/e95fec109c05/zgfazz-27-11-878-img_4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e8/11732385/528cc73e058b/zgfazz-27-11-878-img_1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e8/11732385/7eebce32bed3/zgfazz-27-11-878-img_2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e8/11732385/f19e09f5f31b/zgfazz-27-11-878-img_3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29e8/11732385/e95fec109c05/zgfazz-27-11-878-img_4.jpg

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本文引用的文献

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Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries.2022 年全球癌症统计数据:全球 185 个国家和地区 36 种癌症的发病率和死亡率全球估计数。
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A real-world study and network pharmacology analysis of EGFR-TKIs combined with ZLJT to delay drug resistance in advanced lung adenocarcinoma.一项真实世界研究及网络药理学分析表明,埃克替尼联合中药治疗晚期肺腺癌可延缓耐药。
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Design and Rationale for a Phase II, Randomized, Open-Label, Two-Cohort Multicenter Interventional Study of Osimertinib with or Without Savolitinib in De Novo MET Aberrant, EGFR-Mutant Patients with Advanced Non-Small-Cell Lung Cancer: The FLOWERS Trial.
奥希替尼联合或不联合 savolitinib 治疗初治 MET 外显子 14 跳跃突变、EGFR 突变型晚期非小细胞肺癌的 II 期、随机、开放标签、两队列多中心干预研究的设计和原理: FLOWERS 试验。
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4
Osimertinib + Savolitinib to Overcome Acquired MET-Mediated Resistance in Epidermal Growth Factor Receptor-Mutated, MET-Amplified Non-Small Cell Lung Cancer: TATTON.奥希替尼联合 savolitinib 克服表皮生长因子受体突变、MET 扩增的非小细胞肺癌获得性 MET 介导的耐药:TATTON。
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EGFR signaling pathway as therapeutic target in human cancers.表皮生长因子受体信号通路作为人类癌症的治疗靶点。
Semin Cancer Biol. 2022 Oct;85:253-275. doi: 10.1016/j.semcancer.2022.04.002. Epub 2022 Apr 12.
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Structural Insight and Development of EGFR Tyrosine Kinase Inhibitors.结构洞察与表皮生长因子受体酪氨酸激酶抑制剂的研发。
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INSIGHT 2: a phase II study of tepotinib plus osimertinib in -amplified NSCLC and first-line osimertinib resistance.见解2:特泊替尼联合奥希替尼治疗EGFR基因扩增的非小细胞肺癌及一线奥希替尼耐药的II期研究。
Future Oncol. 2022 Mar;18(9):1039-1054. doi: 10.2217/fon-2021-1406. Epub 2021 Dec 17.
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Afatinib versus erlotinib as second-line treatment of patients with advanced squamous cell carcinoma of the lung: Final analysis of the randomised phase 3 LUX-Lung 8 trial.阿法替尼对比厄洛替尼作为晚期肺鳞状细胞癌患者二线治疗的疗效:3期随机LUX-Lung 8试验的最终分析
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Epidemiology of lung cancer.肺癌流行病学
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