First-Line Treatment in eGFR Mutant non-Small Cell Lung Cancer: is There a Best Option?

被引:15
|
作者
Bulbul, Ajaz [1 ,2 ]
Husain, Hatim [3 ]
机构
[1] Texas Tech Univ, Hlth Sci Ctr, Sch Med, Dept Hematol Oncol, Lubbock, TX 79430 USA
[2] Kymera Independent Phys, Div Hematol Oncol, Hobbs, NM 88240 USA
[3] Univ Calif San Diego, Moores Canc Ctr, La Jolla, CA 92093 USA
来源
FRONTIERS IN ONCOLOGY | 2018年 / 8卷
关键词
lung cancer; epidermal growth factor receptor; targeted therapy; osimertinib; afatinib; gefitinib; erlotinib; OPEN-LABEL; PHASE-III; KINASE INHIBITORS; BRAIN METASTASES; SURVIVAL-DATA; MUTATION; OSIMERTINIB; GEFITINIB; ERLOTINIB; AFATINIB;
D O I
10.3389/fonc.2018.00094
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
First generation or second generation EGFR tyrosine kinase inhibitors are currently the standard of care for the first-line management of non-small cell lung cancer (NSCLC) patients with activating mutations within the kinase domain of the epidermal growth factor receptor gene (1, 2). Resistance to targeted therapy can develop after 9-11 months (3-8). Third generation inhibitors were developed to target the EGFR T790M clone, which is the most common dominant second site resistance mutation after first or second generation inhibitors. Osimertinib received full FDA approval for the second-line treatment of advanced NSCLC based on a phase III study comparing the compound to chemotherapy. Recent data demonstrates an important impact for osimertinib in the front-line space based on results comparing the compound to first-generation erlotinib or gefitinib therapy.
引用
收藏
页数:6
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