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Dacomitinib overcomes acquired resistance to osimertinib in advanced NSCLC patients with EGFR L718Q mutation: A two-case report

奥西默替尼 医学 T790米 吉非替尼 肿瘤科 腺癌 内科学 肺癌 背景(考古学) 表皮生长因子受体 癌症 生物 古生物学 ROS1型
作者
J. li,Meizi Jin,Yuzhu Diao,Li Xiaoling
出处
期刊:Medicine [Wolters Kluwer]
卷期号:103 (28): e38789-e38789 被引量:1
标识
DOI:10.1097/md.0000000000038789
摘要

Rationale: Acquired resistance still inevitably occurs in patients treated with third-generation TKI osimertinib. Although the EGFR L718Q mutation has been reported as a scarce mechanism of osimertinib resistance, advanced therapeutic strategies are still in development. In this report, we included 2 cases of patients who acquired EGFR L858R/L718Q mutation after osimertinib and were overcome by dacomitinib. Patient concerns: Case 1: A 77-year-old woman was diagnosed with stage IV lung adenocarcinoma. Case 2: A 64-year-old woman was diagnosed with stage IV lung adenocarcinoma. Diagnoses: Case 1: The patient was diagnosed with adenocarcinoma with EGFR L858R mutation. Since then, treatment with gefitinib was administrated, leading to a progression-free survival of 18 months. The treatment was switched to osimertinib based on the detection of EGFR T790M mutation, resulting in a progression-free survival of 24 months. Subsequently, EGFR L718Q mutation was detected. Case 2: The patient was diagnosed with adenocarcinoma with EGFR L858R mutation. Icotinib was used as the first-line treatment for 7 months. Osimertinib was applied as the second-line treatment for 13 months based on the EGFR T790M mutation. Subsequently, EGFR L718Q mutation was detected. Interventions: Case 1: Dacomitinib was administered. Case 2: Dacomitinib was administered. Outcomes: Case 1:The progression-free survival was 8 months. Case 2: The progression-free survival was 3 months. Lessons: Dacomitinib is a potential treatment option for NSCLC patients with EGFR L718Q mutation after resistance to Osimertinib. Further research is needed to validate the efficacy of Dacomitinib in this context.

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