Case report: Rechallenge with EGFR-TKIs after immunotherapy in EGFR-mutated non-small cell lung cancer with leptomeningeal metastasis

被引:3
|
作者
Qian, Chunfa [1 ]
Zhang, Yuhai [1 ]
Cheng, Wanwan [2 ]
Zhang, Qingchao [3 ]
Li, Mengzhen [3 ]
Fang, Shencun [2 ]
机构
[1] Nanjing Med Univ, Affiliated Brain Hosp, Dept Neurosurg, Nanjing, Peoples R China
[2] Nanjing Med Univ, Nanjing Chest Hosp, Affiliated Brain Hosp, Dept Resp Med, Nanjing, Peoples R China
[3] MyGene Diagnost Co Ltd, Guangzhou, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2022年 / 12卷
关键词
lung adenocarcinoma; EGFR-TKIs rechallenge; immune checkpoint inhibitor; the third generation EGFR-TKIs; leptomeningeal metastasis;
D O I
10.3389/fonc.2022.957661
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Rechallenge of epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) after PD-1 blockade failure was an effective therapy for non-small cell lung cancer (NSCLC) patients with resistance to EGFR-TKIs. The third-generation TKIs, like osimertinib and furmonertinib, can reach higher concentration in the cerebrospinal fluid (CSF) than other TKIs, and exhibit a beneficial effect in NSCLC patients with leptomeningeal metastases (LM) harboring sensitive EGFR mutation. Here, we report that two-stage IV pulmonary adenocarcinoma patients with LM harboring an EGFR L858R mutation benefit from the third-generation EGFR-TKIs rechallenge after immune checkpoint inhibitor (ICI) and anti-angiogenic agent combination therapy. Complete response (CR) to partial response (PR) of central nervous system (CNS) response was achieved immediately after the administration of furmonertinib and osimertinib. We conducted next-generation sequencing (NGS) and IHC to elucidate the evolution of driver mutations and the immune microenvironment. In conclusion, these two cases might provide a therapeutic strategy for further clinical practice. More research was needed to elucidate the resistance mechanisms and improve current treatment strategies in EGFR-mutated patients with LM.
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页数:5
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