Effectivity and safety of PD-1/PD-L1 inhibitors for different level of PD-L1-positive, advanced NSCLC: A meta-analysis of 4939 patients from randomized controlled trials

被引:7
作者
Shi, Yuanchao [1 ]
Duan, Jingwei [1 ]
Guan, Quanlin [2 ]
Xue, Penglong [3 ]
Zheng, Ya [4 ]
机构
[1] Lanzhou Univ, Clin Acad 1, Lanzhou 730000, Gansu, Peoples R China
[2] Lanzhou Univ, Dept Surg Oncol, Hosp 1, Donggangxi Rd 1st, Lanzhou 730000, Gansu, Peoples R China
[3] Xi An Ninth Hosp, Dept Oncol, Xian 710000, Shaanxi, Peoples R China
[4] Lanzhou Univ, Dept Gastroenterol, Hosp 1, Lanzhou 730000, Gansu, Peoples R China
关键词
Programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) inhibitors; Expression of PD-L1; Non-Small-Lung-cancer; Chemotherapy; CELL LUNG-CANCER; OPEN-LABEL; DOCETAXEL; MULTICENTER; PEMBROLIZUMAB; ATEZOLIZUMAB; NIVOLUMAB;
D O I
10.1016/j.intimp.2020.106452
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Effective improvement for the programmed death 1 (PD-1)/programmed death ligand 1 (PD-L1) inhibitors had been shown in advanced non-small cell lung cancer (NSCLC) patients compared with traditional therapy. However, we do not have ample evidences to demonstrate the safety and effectivity in the treatment of PD-L1-positive, advanced NSCLC. The relation was controversial about the expression of PD-L1 and survival outcomes of PD-1/PD-L1 inhibitors. Materials and methods: Electronic databases (PubMed, EMBASE, and the Cochrane library) and major conference proceedings were systematically searched for all clinical trials in NSCLC using PD-1/PD-L1 inhibitors. Randomized controlled trials (RCTs) were included to compare PD-1/PD-L1 inhibitors with chemotherapy in advanced NSCLC patients reporting adverse events (AEs) and immune-related AEs (irAEs). The incidence, Hazard Ratio (HR), Odds Ratio (OR), and corresponding 95% confidence interval (CI) of outcomes were calculated. Results: A total of 4939 patients from 10RCTs were included. In the group of PD-L1 >= 1%, PD-L1 >= 5%, PD- L1 >= 10%, PD-L1 >= 50%, the HR of OS is 0.31(95%CI 0.38-0.23; p < 0.0001), 0.47(95%CI 0.82-0.12; p = 0.008), 0.85(95%CI 1.17-0.53; p < 0.0001), 0.47(95%CI 0.59-0.36; p < 0.0001) respectively. The HR of PFS is 0.13(95%CI 0.01-0.24; p = 0.027), 0.31(95%CI 0.00-0.62; p < 0.0001), 0.62(95%CI 0.30-0.93; p < 0.0001), 0.40(95% CI 0.20-0.59; p < 0.0001) respectively. In terms of summary adverse events, PD-1/PD-L1 inhibitors groups had a significant lower risks in any treat-realated AEs than chemotherapy. About irAEs, PD-1/PD-L1 inhibitors groups had a significant higher risks in irAEs than chemotherapy. Conclusion: PD-1/PD-L1 inhibitors are generally effected and safer than chemotherapy for patients with PD-L1-positive, advanced NSCLC. However, PD-1/PD-L1 inhibitors can generate a unique spectrum of irAEs, and even life-threatening.
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页数:7
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