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不同 PD-L1 阳性表达水平的晚期 NSCLC 患者接受 PD-1/PD-L1 抑制剂治疗的有效性和安全性:来自随机对照试验的 4939 例患者的荟萃分析。

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.

机构信息

The Lanzhou University, The First Clinical Academy of Lanzhou University, Lanzhou 730000, Gansu, China.

Department of Surgical Oncology, The Lanzhou University First Hospital, Lanzhou 730000, Gansu, China.

出版信息

Int Immunopharmacol. 2020 Jul;84:106452. doi: 10.1016/j.intimp.2020.106452. Epub 2020 Apr 24.

Abstract

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.

摘要

背景

与传统疗法相比,程序性死亡 1(PD-1)/程序性死亡配体 1(PD-L1)抑制剂在晚期非小细胞肺癌(NSCLC)患者中显示出了有效的改善。然而,我们没有充分的证据来证明 PD-L1 阳性、晚期 NSCLC 患者的治疗中使用 PD-1/PD-L1 抑制剂的安全性和有效性。PD-L1 的表达与 PD-1/PD-L1 抑制剂的生存结局之间的关系存在争议。

材料和方法

系统地检索了使用 PD-1/PD-L1 抑制剂治疗 NSCLC 的所有临床试验的电子数据库(PubMed、EMBASE 和 Cochrane 图书馆)和主要会议记录。纳入了比较 PD-1/PD-L1 抑制剂与化疗治疗晚期 NSCLC 患者不良事件(AE)和免疫相关不良事件(irAE)的随机对照试验(RCT)。计算了结局的发生率、风险比(HR)、优势比(OR)和相应的 95%置信区间(CI)。

结果

共有来自 10 项 RCT 的 4939 名患者被纳入研究。在 PD-L1≥1%、PD-L1≥5%、PD-L1≥10%、PD-L1≥50%的组中,OS 的 HR 为 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)和 0.47(95%CI 0.59-0.36;p<0.0001)。PFS 的 HR 为 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)和 0.40(95%CI 0.20-0.59;p<0.0001)。在总结不良事件方面,PD-1/PD-L1 抑制剂组发生任何治疗相关 AE 的风险明显低于化疗组。关于 irAEs,PD-1/PD-L1 抑制剂组发生 irAEs 的风险明显高于化疗组。

结论

对于 PD-L1 阳性、晚期 NSCLC 患者,PD-1/PD-L1 抑制剂通常比化疗更有效且更安全。然而,PD-1/PD-L1 抑制剂会产生独特的 irAEs 谱,甚至危及生命。

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