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奥希替尼(AZD9291)耐药的基于异质性、多种机制:病例报告。

Heterogeneity-based, multiple mechanisms in the resistance to osimertinib (AZD9291): A case report.

机构信息

Department of Medical Oncology, Beijing Key Laboratory of Clinical Study on Anticancer Molecular Targeted Drugs, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

Department of Pathology, National Cancer Center/Cancer Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China.

出版信息

Thorac Cancer. 2018 Apr;9(4):498-501. doi: 10.1111/1759-7714.12596. Epub 2018 Feb 7.

Abstract

Osimertinib is a novel, irreversible, mutant-selective epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor targeting EGFR mutations and the EGFR T790 mutation. Here, we report a woman with EGFR-mutated lung adenocarcinoma who, after 23-month treatment with gefitinib, developed the EGFR T790M mutation, which converted the T790M status from positive to negative before osimertinib treatment and developed MET amplification, leading to rapid progression on osimertinib in two months. Subsequent treatment with crizotinib and c-Met inhibitor plus gefitinib also failed to improve the clinical outcome, suggesting the potential existence of another resistance mechanism. Our findings revealed the underlying multiple and heterogeneous mechanisms in resistance to osimertinib, suggesting combination strategies should be considered post-osimertinib progression.

摘要

奥希替尼是一种新型、不可逆、突变选择性表皮生长因子受体(EGFR)酪氨酸激酶抑制剂,针对 EGFR 突变和 EGFR T790 突变。在这里,我们报告了一例 EGFR 突变型肺腺癌患者,在接受吉非替尼治疗 23 个月后,出现了 EGFR T790M 突变,在奥希替尼治疗前,T790M 状态由阳性转为阴性,并发生了 MET 扩增,导致奥希替尼治疗两个月内迅速进展。随后使用克唑替尼和 c-Met 抑制剂加吉非替尼治疗也未能改善临床结局,提示可能存在另一种耐药机制。我们的研究结果揭示了奥希替尼耐药的潜在多种和异质性机制,提示在奥希替尼进展后应考虑联合治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e86/5879057/249ba16c4f7d/TCA-9-498-g001.jpg

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