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EGFR L718Q mutation occurs without T790M mutation in a lung adenocarcinoma patient with acquired resistance to osimertinib
被引:26
|作者:
Ma, Lei
[1
]
Chen, Rui
[1
]
Wang, Fang
[1
]
Ma, Li-Li
[1
]
Yuan, Ming-Ming
[2
]
Chen, Rong-Rong
[2
]
Liu, Jiang
[1
]
机构:
[1] Peoples Hosp Xinjiang Uygur Autonomous Reg, Dept Oncol, 91 Tianchi Rd, Urumqi 830001, Peoples R China
[2] Geneplus Beijing Inst, Beijing 102206, Peoples R China
关键词:
Non-small cell lung cancer (NSCLC);
epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs);
EGFR L718Q;
osimertinib resistance;
AZD9291;
D O I:
10.21037/atm.2019.04.37
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) improve the clinical outcomes of EGFR-mutant non-small cell lung cancer (NSCLC) patients significantly, however, acquired resistance occurs almost inevitably. The underlying mechanisms of osimertinib resistance and treatment strategies after resistance remain largely unknown. Here we reported a case of lung adenocarcinoma patient who progressed on osimertinib with EGFR L718Q mutation in the absence of T790M mutation. The patient received icotinib as an exploratory treatment regimen for a short while with stable disease observed. Unfortunately, the therapy was discontinued due to intolerable hepatotoxicity. This is the first clinical report of the use of the effective EGFR-TKI treatment after L718Q-induced osimertinib resistance. The therapeutic regimens for NSCLC patients progressed on osimertinib still require large-scale investigation.
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