Optimizing outcomes in EGFR mutation-positive NSCLC: which tyrosine kinase inhibitor and when?

被引:87
|
作者
Girard, Nicolas [1 ,2 ]
机构
[1] Univ Claude Bernard Lyon 1, Univ Lyon, Thorac Oncol, F-69622 Lyon, France
[2] Inst Curie, Inst Thorax Curie Montsouris, Thorac Surg, F-75248 Paris, France
关键词
afatinib; dacomitinib; EGFR; erlotinib; gefitinib; non-small-cell lung cancer; osimertinib; resistance; treatment sequencing; T790M; CELL LUNG-CANCER; GROWTH-FACTOR RECEPTOR; OPEN-LABEL; 1ST-LINE TREATMENT; PHASE-III; ACQUIRED-RESISTANCE; BRAIN METASTASIS; CARBOPLATIN-PACLITAXEL; GENE-MUTATIONS; SURVIVAL-DATA;
D O I
10.2217/fon-2017-0636
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite the efficacy of standard-of-care EGFR tyrosine kinase inhibitors (TKIs), erlotinib, gefitinib and afatinib, in EGFR mutation-positive non-small-cell lung cancer, resistance develops, most commonly due to the T790M mutation. Osimertinib showed clinical activity in the treatment of T790M-positive disease following progression on a first-line TKI, and is approved in this setting. Recently, osimertinib improved efficacy versus first-generation TKIs (erlotinib and gefitinib) in the first-line setting. Multiple factors can influence first-line treatment decisions, including subsequent therapy options, presence of brain metastases and tolerability, all of which should be considered in the long-term treatment plan. Further research into treatment sequencing is also needed, to optimize outcomes in EGFR mutation-positive non-small-cell lung cancer.
引用
收藏
页码:1117 / 1132
页数:16
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