Efficacy of anti-PD-1 antibodies in NSCLC patients with anEGFRmutation and high PD-L1 expression

被引:52
作者
Masuda, Ken [1 ]
Horinouchi, Hidehito [1 ]
Tanaka, Midori [1 ]
Higashiyama, Ryoko [1 ]
Shinno, Yuki [1 ]
Sato, Jun [2 ]
Matsumoto, Yuji [1 ]
Okuma, Yusuke [1 ]
Yoshida, Tatsuya [1 ]
Goto, Yasushi [1 ]
Yamamoto, Noboru [1 ,2 ]
Ohe, Yuichiro [1 ]
机构
[1] Natl Canc Ctr, Dept Thorac Oncol, Chuo Ku, 5-1-1 Tsukiji, Tokyo 1040045, Japan
[2] Natl Canc Ctr, Dept Expt Therapeut, Tokyo, Japan
关键词
Non-small cell lung cancer; Programmed death-ligand-1; Epidermal growth factor receptor; Immune checkpoint inhibitor; CELL LUNG-CANCER; OPEN-LABEL; DOCETAXEL; NIVOLUMAB; PEMBROLIZUMAB; ATEZOLIZUMAB; MULTICENTER; SURVIVAL; BLOCKADE;
D O I
10.1007/s00432-020-03329-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction Several studies have demonstrated that non-small cell lung cancer patients (NSCLCs) harboring epidermal growth factor receptor (EGFR) mutations have poor clinical outcomes in response to treatment with programmed death-1 (PD-1) inhibitors. However, it remains unclear whether EGFR-mutated NSCLCs with a high programmed death-ligand-1 (PD-L1) expression (tumor proportion score >= 50%) respond to PD-1 inhibitors. Methods We retrospectively investigated the NSCLCs who had received PD-1 inhibitors between January 2016 and December 2018 to assess the efficacy of PD-1 inhibitors in patients with anEGFRmutation and high PD-L1 expression. Results There were 153 patients with a high PD-L1 expression level, and the median progression-free survival (mPFS) was 5.3 months [95% confidence interval (CI) 1.3-12.4 months] in the patients withEGFRmutations (n = 17) and 8.3 months (95% CI 6.0-11.7 months) in those with wild-typeEGFR(n = 136; hazard ratio (HR) 1.62; 95% CI 0.83-2.87). Among the 110 patients in the low PD-L1 expression group, the mPFS was 1.6 months (95% CI 1.3-5.9 months) in the patients withEGFRmutations (n = 18) and 3.8 months (95% CI 2.5-5.9 months) in those with wild-typeEGFR(n = 92; HR 2.59; 95% CI 1.48-4.31). The HR for PFS in the group withEGFRmutations and high PD-L1 expression was 0.97 (95% CI 0.56-1.59) compared to the group with wild-typeEGFRand low PD-L1 expression. Conclusions PD-1 inhibitors can serve as one of the treatment options for NSCLCs with anEGFRmutation and high PD-L1 expression.
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页码:245 / 251
页数:7
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