Progress in individualized treatment for EGFR-mutated advanced non-small cell lung cancer

被引:6
作者
Inoue, Akira [1 ]
机构
[1] Tohoku Univ, Dept Palliat Med, Sch Med, Sendai, Miyagi, Japan
来源
PROCEEDINGS OF THE JAPAN ACADEMY SERIES B-PHYSICAL AND BIOLOGICAL SCIENCES | 2020年 / 96卷 / 07期
关键词
lung cancer; EGFR-TKI; EGFR mutation; chemotherapy; GROWTH-FACTOR RECEPTOR; PREVIOUSLY TREATED PATIENTS; CISPLATIN PLUS GEMCITABINE; RANDOMIZED PHASE-III; 1ST-LINE TREATMENT; OPEN-LABEL; CARBOPLATIN-PACLITAXEL; GEFITINIB; MUTATIONS; CHEMOTHERAPY;
D O I
10.2183/pjab.96.020
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The identification of mutations in the epidermal growth factor receptor (EGFR) gene has revolutionized the treatment strategy for non-small cell lung cancer (NSCLC). The effectiveness of individualized treatment using EGFR tyrosine kinase inhibitors (TKIs) for EGFR-mutated NSCLC has mainly been clarified in clinical trials within Japan, and EGFR-TKI monotherapy has been established as the standard first-line treatment for EGFR-mutated NSCLC. Since then, combination regimens involving EGFR-TKI and chemotherapy or anti-angiogenic agents have been developed. Regarding combinations, the NEJ009 study conducted in Japan showed a significant prolongation of progression-free survival and overall survival compared with gefitinib alone. The NEJ009 regimen may be a reasonable option for patients with good performance status in terms of risk-benefit balance. However, further investigation is warranted to improve clinical outcomes in EGFR-mutated NSCLC.
引用
收藏
页码:266 / 272
页数:7
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