Yang Jie, Yu Haizan, Zhang Yilei, Zhu Mingli, Zhang Mengyu, Wang Qiming
Department of Gynaecology, III, Women's and Children's Hospital of Ningbo University, Ningbo, Zhejiang, China.
Front Oncol. 2024 Aug 20;14:1454372. doi: 10.3389/fonc.2024.1454372. eCollection 2024.
To assess the effectiveness and tolerability of both PD-1 and PD-L1 inhibitors in advanced cervical cancer (CC), focusing on varying PD-L1 levels.
A comprehensive exploration was carried out on EMBASE, PubMed, Cochrane Library databases as well as Web of Science up to May 25, 2024, for studies involving advanced CC patients receiving PD-1/PD-L1 inhibitors. Inclusion criteria were studies reporting objective response rate (ORR), disease control rate (DCR), median progression-free survival (PFS), as well as median overall survival (OS). Data extraction and quality assessment were performed by two reviewers using the JBI Case Series Critical Appraisal Checklist, followed by a meta-analysis via STATA/MP 16.0.
Five eligible studies comprising 223 patients were chosen. ORR and DCR were 42% (95% CI: 17%-66%, P = 0.00) and 70% (95% CI: 22%-117%, P = 0.00), respectively, in the PD-L1 positive patients and were 36% (95% CI: 17%-54%, P = 0.00) and 47% (95% CI: 30%-63%, P = 0.00), respectively, in patients with PD-L1 negativity. For patients exhibiting PD-L1 positivity, median PFS and median OS were 3.98 months (95% CI: 0.80-7.16, P = 0.01) and 11.26 months (95% CI: 3.01-12.58, P = 0.00), respectively.
With PD-1/PD-L1 inhibitors, PD-L1 positive CC patients demonstrate superior ORR, DCR, median PFS, and median OS, underscoring PD-L1 as one biomarker for immunotherapy response.
评估程序性死亡受体1(PD-1)抑制剂和程序性死亡配体1(PD-L1)抑制剂在晚期宫颈癌(CC)中的有效性和耐受性,重点关注不同的PD-L1水平。
截至2024年5月25日,对EMBASE、PubMed、Cochrane图书馆数据库以及Web of Science进行了全面检索,以查找涉及接受PD-1/PD-L1抑制剂治疗的晚期CC患者的研究。纳入标准为报告客观缓解率(ORR)、疾病控制率(DCR)、中位无进展生存期(PFS)以及中位总生存期(OS)的研究。由两名审阅者使用JBI病例系列关键评估清单进行数据提取和质量评估,随后通过STATA/MP 16.0进行荟萃分析。
选择了五项符合条件的研究,共223例患者。PD-L1阳性患者的ORR和DCR分别为42%(95%置信区间:17%-66%,P = 0.00)和70%(95%置信区间:22%-117%,P = 0.00),而PD-L1阴性患者的ORR和DCR分别为36%(95%置信区间:17%-54%,P = 0.00)和47%(95%置信区间:30%-63%,P = 0.00)。对于表现出PD-L1阳性的患者,中位PFS和中位OS分别为3.98个月(95%置信区间:0.80-7.16,P = 0.01)和11.26个月(95%置信区间:3.01-12.58,P = 0.00)。
对于接受PD-1/PD-L1抑制剂治疗的患者,PD-L1阳性的CC患者表现出更高的ORR、DCR、中位PFS和中位OS,这突出了PD-L1作为免疫治疗反应的一个生物标志物。