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首页> 外文期刊>Journal of Cancer Research and Clinical Oncology >Efficacy of anti-PD-1 antibodies in NSCLC patients with anEGFRmutation and high PD-L1 expression
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Efficacy of anti-PD-1 antibodies in NSCLC patients with anEGFRmutation and high PD-L1 expression

机译:抗PD-1抗体在NSCLC患者患者抗折叠和高PD-L1表达中的疗效

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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.
机译:导言一些研究表明,携带表皮生长因子受体(EGFR)突变的非小细胞肺癌患者(NSCLC)对程序性死亡-1(PD-1)抑制剂的治疗反应不佳。然而,目前尚不清楚具有高程序性死亡配体-1(PD-L1)表达(肿瘤比例评分>=50%)的EGFR突变NSCLC是否对PD-1抑制剂产生反应。方法我们回顾性调查了2016年1月至2018年12月期间接受PD-1抑制剂治疗的NSCLC,以评估PD-1抑制剂对无基因突变和PD-L1高表达患者的疗效。结果共有153例PD-L1高表达患者,EGFR突变组(n=17)的中位无进展生存期(mPFS)为5.3个月[95%可信区间(CI)1.3-12.4个月],野生型EGFR组(n=136;风险比(HR)1.62;95%可信区间0.83-2.87)。在PD-L1低表达组的110名患者中,EGFR突变组(n=18)的MPF为1.6个月(95%CI 1.3-5.9个月),野生型EGFR组(n=92;HR 2.59;95%CI 1.48-4.31)的MPF为3.8个月(95%CI 2.5-5.9个月)。与野生型EGF和低PD-L1表达组相比,EGFR突变和PD-L1高表达组的PFS HR为0.97(95%可信区间0.56-1.59)。结论PD-1抑制剂可作为治疗无基因突变和PD-L1高表达NSCLC的一种选择。

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