Sun Chenxi, Chen Huixian, Wang Yongjing, Zheng Chengyun
The Second Hospital of Shandong University, Jinan, Shandong, People's Republic of China.
Center for Clinical Research, The Affiliated Hospital of Qingdao University, Qingdao, People's Republic of China.
Hematology. 2023 Dec;28(1):2181749. doi: 10.1080/16078454.2023.2181749.
Inhibitors of programmed cell death protein 1 (PD-1) and programmed cell death ligand 1 (PD-L1) have been used in the treatment of relapsed and refractory Hodgkin's lymphoma (R/R HL) recently. To further understand the safety and efficacy of PD-1/PD-L1 inhibitors in R/R HL, we conducted this meta-analysis.
Databases and the Clinical Registration Platforms have been systematically searched for related studies by March 2022. For safety analysis, the incidence and exhibition of any grade and grade 3 or higher adverse effects (AEs) were evaluated. Besides, severe AEs (SAEs), treatment-related deaths, and AEs leading to treatment discontinuation were summarized. The overall response rate (ORR), complete response (CR) rate, partial response (PR) rate, progression-free survival (PFS), overall survival (OS), and duration of response (DOR) were calculated for efficacy analysis. All processes were implemented mainly through the package Meta and MetaSurv of software R 4.1.2.
Overall 20 studies and 1440 patients were enrolled. The pooled incidence of any grade and grade 3 or higher AEs were 92% and 26%, respectively. The pooled ORR, CR rate and PR rate were 79%, 44% and 34%, respectively. The most common AEs were neuropathy (29%), nausea (27%), pyrexia (26%), and leukopenia (25%), and the most common grade 3 or higher AEs included leukopenia (10%), infusion reaction (8%), weight gain (3%), and neutropenia (2.7%). In survival analysis, pembrolizumab monotherapy appeared to perform better compared to nivolumab monotherapy.
PD-1/PD-L1 inhibitors show promising efficacy and tolerable AEs in the treatment of R/R HL.
程序性细胞死亡蛋白1(PD-1)和程序性细胞死亡配体1(PD-L1)抑制剂最近已用于复发难治性霍奇金淋巴瘤(R/R HL)的治疗。为了进一步了解PD-1/PD-L1抑制剂在R/R HL中的安全性和疗效,我们进行了这项荟萃分析。
截至2022年3月,我们系统检索了数据库和临床注册平台中的相关研究。对于安全性分析,评估了任何级别以及3级或更高级别不良反应(AE)的发生率和表现。此外,总结了严重AE(SAE)、治疗相关死亡以及导致治疗中断的AE。计算总缓解率(ORR)、完全缓解(CR)率、部分缓解(PR)率、无进展生存期(PFS)、总生存期(OS)和缓解持续时间(DOR)用于疗效分析。所有过程主要通过软件R 4.1.2的Meta和MetaSurv包实现。
共纳入20项研究和1440例患者。任何级别和3级或更高级别AE的合并发生率分别为92%和26%。合并的ORR、CR率和PR率分别为79%、44%和34%。最常见的AE为神经病变(29%)、恶心(27%)、发热(26%)和白细胞减少(25%),最常见的3级或更高级别AE包括白细胞减少(10%)、输液反应(8%)、体重增加(3%)和中性粒细胞减少(2.7%)。在生存分析中,帕博利珠单抗单药治疗似乎比纳武利尤单抗单药治疗表现更好。
PD-1/PD-L1抑制剂在R/R HL治疗中显示出有前景的疗效和可耐受的AE。