阿替唑单抗
医学
多西紫杉醇
肿瘤科
内科学
克拉斯
危险系数
肺癌
癌症
彭布罗利珠单抗
置信区间
免疫疗法
结直肠癌
作者
Chenyue Zhang,Kai Wang,Jiamao Lin,Haiyong Wang
出处
期刊:Future Oncology
[Future Medicine]
日期:2022-09-01
卷期号:18 (27): 3031-3041
被引量:7
标识
DOI:10.2217/fon-2022-0295
摘要
Aim: To explore the association between TP53 mutation and atezolizumab in non-small-cell lung cancer (NSCLC) patients. Materials & methods: Patients with NSCLC from the POPLAR and OAK studies were included. Kaplan-Meier analysis was performed to detect progression-free survival (PFS) and overall survival (OS). PFS and OS were compared using multivariate Cox regression analysis. Results: OS was significantly longer with atezolizumab compared with docetaxel among TP53/KRAS co-mutant NSCLC patients (hazard ratio [HR]: 0.014; 95% CI: 0.000-0.721). There is no significant OS difference between atezolizumab versus docetaxel for TP53-mutant NSCLC patients (HR: 0.831; 95% CI: 0.473-1.458). There is no significant OS difference between atezolizumab versus docetaxel for KRAS-mutant NSCLC patients (HR: 1.354; 95% CI: 0.528-3.472). Conclusion: PD-L1 inhibitors may bring OS benefits for patients with NSCLC harbored TP53/KRAS co-mutation.
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