Clinical efficacy and safety of afatinib in the treatment of non-small-cell lung cancer in Chinese patients

被引:14
|
作者
Wang, Lei-Yun [1 ,2 ]
Cui, Jia-Jia [1 ,2 ]
Guo, Ao-Xiang [1 ,2 ]
Yin, Ji-Ye [1 ,2 ]
机构
[1] Cent South Univ, XiangYa Hosp, Dept Clin Pharmacol, 110 XiangYa Rd, Changsha 410008, Hunan, Peoples R China
[2] Cent South Univ, Inst Clin Pharmacol, Hunan Key Lab Pharmacogenet, Changsha, Hunan, Peoples R China
来源
ONCOTARGETS AND THERAPY | 2018年 / 11卷
基金
中国国家自然科学基金;
关键词
afatinib; NSCLC; Chinese patients; drug resistance; side effect; companion diagnosis; FACTOR RECEPTOR MUTATIONS; EGFR GENE MUTATION; SOMATIC MUTATIONS; ACQUIRED-RESISTANCE; 1ST-LINE TREATMENT; SIGNALING PATHWAY; DRIVER MUTATIONS; ASIAN PATIENTS; KINASE DOMAIN; OPEN-LABEL;
D O I
10.2147/OTT.S136579
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Compared with various malignant tumors, lung cancer has high incidence and the highest mortality worldwide. Non-small-cell lung cancer (NSCLC), the most common kind of lung cancer, is still a great threat to the world, including China. Surgery, platinum-based chemotherapy, and radiotherapy are still the primary treatments for NSCLC patients in the clinic, whereas immunotherapy and targeted therapy are gradually playing more important roles. A next-generation tyrosine kinase inhibitor (TKI), afatinib, was developed as a targeted reagent for epidermal growth factor receptor (EGFR). This targeted drug was effective in a series of trials. The US Food and Drug Administration then approved afatinib as a new first-line treatment for EGFR L858R and exon 19 deletion mutant patients in 2013. This review focused on current clinical studies of afatinib. Although this TKI was not widely available in China until recently, we aim to provide a reference for its future use in China.
引用
收藏
页码:529 / 538
页数:10
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