Efficacy of epidermal growth factor receptor-tyrosine kinase inhibitor for lung adenosquamous cell carcinoma harboring EGFR mutation: a retrospective study and pooled analysis

被引:0
|
作者
Xia, Xueming [1 ]
Du, Wei [2 ]
Zhang, Yan [3 ]
Li, Yanying [3 ]
Yu, Min [3 ]
Liu, Yongmei [3 ]
机构
[1] Sichuan Univ, West China Hosp, Canc Ctr, Div Head & Neck Tumor Multimodal Treatment, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, Canc Ctr, Dept Targeting Therapy & Immunol, Chengdu, Peoples R China
[3] Sichuan Univ, West China Hosp, Canc Ctr, Div Thorac Tumor Multimodal Treatment, Chengdu, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2024年 / 14卷
关键词
tyrosine kinase inhibitor; adenosquamous lung carcinoma; EGFR; mutation; lung cancer; GENE-MUTATIONS; PHASE-III; CANCER; GEFITINIB; ERLOTINIB; SURVIVAL; TKI; CHEMOTHERAPY; RESISTANCE; AFATINIB;
D O I
10.3389/fonc.2024.1354854
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives To explore the efficacy of epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) on lung adenosquamous cell carcinoma (ASC) with EGFR mutation.Methods Efficacy of EGFR-TKIs in the treatment of advanced or recurrent lung ASC with EGFR mutations was assessed retrospectively in 44 patients. Pooled analysis of 74 patients using EGFR-TKIs, including 30 patients selected from 11 publications, was conducted.Results In our retrospective research, patients treated with EGFR-TKI in ASC with EGFR mutations had objective response rate (ORR) of 54.5%, disease control rate (DCR) of 79.5%, median progression free survival (mPFS) of 8.8 months, and median overall survival (mOS) of 19.43 months, respectively. A pooled analysis reveals ORR, DCR, mPFS, and mOS are, respectively, 63.4%, 85.9%, 10.00 months, and 21.37 months for ASC patients. In patients with deletions in exon 19 and exon 21 L858R mutations, mPFS (11.0 versus 10.0 months, P=0.771) and mOS (23.67 versus 20.33 months, P=0.973) were similar. Erlotinib or gefitinib-treated patients had an overall survival trend that was superior to that of icotinib-treated patients.Conclusions ASC harboring EGFR mutations can be treated with EGFR-TKI in a similar manner to Adenocarcinoma (ADC) harboring EGFR mutations. There is still a need for further investigation to identify the separate roles of ASC's two components in treating EGFR.
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页数:8
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