LUO Hongmei,ZOU Jiafeng,ZHAO Jiufeng,et al.Meta-analysis of the efficacy and safety of PD-1/PD-L1 inhibitors combined with bevacizumab in the treatment of advanced non-small cell lung cancer[J].ZHONGGUO YAOFANG,2024,35(23):2923-2928.
LUO Hongmei,ZOU Jiafeng,ZHAO Jiufeng,et al.Meta-analysis of the efficacy and safety of PD-1/PD-L1 inhibitors combined with bevacizumab in the treatment of advanced non-small cell lung cancer[J].ZHONGGUO YAOFANG,2024,35(23):2923-2928. DOI: 10.6039/j.issn.1001-0408.2024.23.14.
Meta-analysis of the efficacy and safety of PD-1/PD-L1 inhibitors combined with bevacizumab in the treatment of advanced non-small cell lung cancer
检索中国知网、万方、维普、Web of Science、PubMed等中英文数据库,检索时间为建库至2024年4月25日。收集含铂双药联合PD-1/PD-L1抑制剂及贝伐珠单抗(试验组)对比含铂双药联合或不联合PD-1/PD-L1抑制剂或贝伐珠单抗(对照组)治疗晚期非小细胞肺癌的队列研究或随机对照试验。筛选文献、提取数据并进行文献质量评价后,采用RevMan 5.4.1软件进行Meta分析和敏感性分析。
To evaluate the efficacy and safety of programmed death-1/programmed death-ligand 1 (PD-1/PD-L1) inhibitors combined with bevacizumab in the treatment of advanced non-small cell lung cancer (NSCLC) based on platinum-containing dual therapy.
METHODS
2
Retrieved from CNKI, Wanfang, VIP, Web of Science, PubMed and other Chinese and English databases, cohort studies or randomized controlled trial studies on the treatment of advanced NSCLC with platinum-containing double agents in combination with PD-1/PD-L1 inhibitors and bevacizumab (trial group) versus platinum-containing double agents with or without PD-1/PD-L1 inhibitor or bevacizumab (control group) were collected from the inception to April 25, 2024. After screening literature, extracting data and evaluating quality, meta-analysis and sensitivity analysis were performed by using RevMan 5.4.1 software.
RESULTS
2
A total of 15 pieces of literature were included, involving 13 clinical studies with a total of 3 282 patients. Compared with the control group, partial response rate [RR=0.75,95%CI(0.68,0.82),
and disease control rate (DCR) [RR=0.85, 95%CI (0.77,0.95),
P
=0.003
]
were higher in the trial group. There w
as no statistically significant difference in the stable disease rate [RR=1.25, 95%CI (0.86, 1.83),
P
=0.25
]
or overall adverse drug reaction incidence rate [RR=0.95, 95%CI (0.90, 1.00),
P
=0.07
]
between the two groups of patients. Sensitivity analyses showed robust and reliable results for all outcome indicators.
CONCLUSIONS
2
PD-1/PD-L1 inhibitors combined with bevacizumab based on platinum-containing dual therapy in the treatment of advanced NSCLC can improve patients’ clinical benefits, such as ORR and DCR, without increasing the risk of adverse drug reaction.
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