Effectiveness of PD1/PD-L1 combined with anti-angiogenic drugs in patients with advanced nonsmall cell lung cancer: A systematic review and meta-analysis.

IF 1.5 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
Journal of Research in Medical Sciences Pub Date : 2024-02-23 eCollection Date: 2024-01-01 DOI:10.4103/jrms.jrms_166_23
Xueyu Duan, Xiaobo Liu, Ruixiang Chen, Yanjiao Pu
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引用次数: 0

Abstract

Background: Protein-1 (PD-1) and programmed cell death 1 ligand 1 (PD-L1) therapy have become an important treatment approach for patients with advanced nonsmall cell lung cancer (NSCLC), but primary or secondary resistance remains a challenge for some patients. PD-1/PD-L1 combined with anti-angiogenic drugs (AAs) in NSCLC patients have potential synergistic effects, and the survival benefit may vary based on a treatment order. To investigate the efficacy of PD-1/PD-L1 combined with AAs as the treatment for patients with advanced NSCLC.

Materials and methods: We comprehensively searched EMBASE, PubMed, Web of Science, CNKI, VIP, and Wanfang databases from January 2017 to September 2022. The Cochrane risk bias tool evaluated the quality of included randomized clinical trials. Newcastle-Ottawa-Scale score was used to evaluate the quality of retrospective studies. Publication bias was evaluated by funnel plot, Begg's test, and Egger's test.

Results: Seventeen articles were finally selected, involving 5182 patients. Meta-analysis results showed that PD1/PD-L1 combined with AAs therapy significantly improved progression-free survival (PFS) (hazard ratio [HR] = 0.61, 95% confidence interval [CI]: 0.50-0.75, P < 0.00001), overall survival (OS) (HR = 0.79, 95% CI: 0.71-0.88, P < 0.00001), and objective response rate (ORR) (risk ratio = 0.88, 95% CI: 0.81-0.96, P = 0.004), with the statistically significant difference. The sensitivity analysis demonstrated the robustness of the PFS, ORR, and OS.

Conclusion: The combination of PD-1/PD-L1 inhibitors with AAs in treating advanced patients has exhibited notable therapeutic advantages when contrasted with monotherapy. Specifically, the administration of PD-1/PD-L1 inhibitors in conjunction with AAs, or sequential treatment involving PD-1/PD-L1 followed by AAs, has shown enhanced therapeutic efficacy in this patient population.

PD1/PD-L1 联合抗血管生成药物对晚期非小细胞肺癌患者的疗效:系统综述与荟萃分析。
背景:蛋白-1(PD-1)和程序性细胞死亡1配体1(PD-L1)疗法已成为晚期非小细胞肺癌(NSCLC)患者的重要治疗方法,但原发性或继发性耐药性仍是一些患者面临的挑战。PD-1/PD-L1与抗血管生成药物(AAs)联合治疗NSCLC患者具有潜在的协同作用,其生存获益可能因治疗顺序而异。研究PD-1/PD-L1联合AAs治疗晚期NSCLC患者的疗效:我们全面检索了2017年1月至2022年9月的EMBASE、PubMed、Web of Science、CNKI、VIP和万方数据库。Cochrane风险偏倚工具评估了纳入的随机临床试验的质量。纽卡斯尔-渥太华量表评分用于评估回顾性研究的质量。通过漏斗图、Begg's 检验和 Egger's 检验评估发表偏倚:最终选取了 17 篇文章,涉及 5182 名患者。Meta分析结果显示,PD1/PD-L1联合AAs疗法可显著改善无进展生存期(PFS)(危险比[HR] = 0.61,95%置信区间[CI]:0.50-0.75,P < 0.00001)、总生存期(OS)(HR = 0.79,95% CI:0.71-0.88,P < 0.00001)和客观反应率(ORR)(风险比 = 0.88,95% CI:0.81-0.96,P = 0.004),差异有统计学意义。敏感性分析表明了PFS、ORR和OS的稳健性:结论:PD-1/PD-L1抑制剂与AAs联合治疗晚期患者与单一疗法相比具有明显的治疗优势。具体来说,PD-1/PD-L1抑制剂与AAs联合使用,或先使用PD-1/PD-L1抑制剂再使用AAs进行序贯治疗,都能提高这类患者的疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Research in Medical Sciences
Journal of Research in Medical Sciences MEDICINE, GENERAL & INTERNAL-
CiteScore
2.60
自引率
6.20%
发文量
75
审稿时长
3-6 weeks
期刊介绍: Journal of Research in Medical Sciences, a publication of Isfahan University of Medical Sciences, is a peer-reviewed online continuous journal with print on demand compilation of issues published. The journal’s full text is available online at http://www.jmsjournal.net. The journal allows free access (Open Access) to its contents and permits authors to self-archive final accepted version of the articles on any OAI-compliant institutional / subject-based repository.
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