吉非替尼
医学
表皮生长因子受体
肺癌
内科学
肿瘤科
化疗
吉西他滨
卡铂
性能状态
培美曲塞
埃罗替尼
癌症
顺铂
作者
Hong Jian,Wěi Li,Zhiyong Ma,Jianjin Huang,Jifeng Feng,Yong Song,Beili Gao,Huili Zhu,Min Tao,Chong Bai,Shenglin Ma,Hongming Pan,Shukui Qin,Dong Hua,Yongfeng Yu,Shun Lü
标识
DOI:10.1038/s41598-017-08399-8
摘要
Abstract Epidermal growth factor receptor tyrosine-kinase inhibitors (EGFR-TKIs) are standard treatment for advanced non-small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) mutation. However, EGFR mutation testing is not attainable in approximately 20% of patients. The current study examined intercalating and maintaining gefitinib treatment in stage IIIB/IV non-squamous NSCLC, never or former light smoking patients with unknown EGFR mutation status. Briefly, 219 patients who achieved stable disease (SD) with gemcitabine (1250 mg/m 2 ) plus carboplatin (5 AUC) were randomized at 1:1 ratio to continue chemotherapy (n = 110) or intercalating gefitinib (250 mg/day on days 15–25 of each cycle until disease progress (n = 109). Progression-free survival (PFS) was 9.7 vs. 4.2 month in the gefitinib vs. control arm (HR: 0.41, 95% CI: 0.31–0.56; P < 0.001). Overall survival (OS) was also longer in the gefitinib arm (20.1 vs. 15.4 months; HR: 0.68; 95% CI 0.48–0.97; P = 0.0323). Adverse events, including diarrhea, dermal reaction and thrombocytopenia, were more common in the gefitinib arm. In conclusion, intercalating and maintenance gefitinib treatment is a viable option for advanced NSCLC patients with unknown EGFR mutation status in subpopulations with high EFGR mutation rate.
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