Nuerbiyamu Maimaitiyiming, Yue Li, Yunfeng Cao, Yanwei Li
{"title":"以康瑞珠单抗为基础的非小细胞肺癌综合治疗的有效性和安全性:系统综述和荟萃分析。","authors":"Nuerbiyamu Maimaitiyiming, Yue Li, Yunfeng Cao, Yanwei Li","doi":"10.1177/17588359241284904","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Many studies show that camrelizumab combination therapy can significantly improve progression-free survival (PFS) and overall survival (OS) in non-small cell lung cancer (NSCLC). However, the time of camrelizumab to market is short, and there is no systematic evaluation of camrelizumab-based comprehensive treatment of NSCLC.</p><p><strong>Objectives: </strong>To systematically evaluate the efficacy and safety of camrelizumab in comprehensively treating NSCLC.</p><p><strong>Design: </strong>A systematic review and meta-analysis.</p><p><strong>Data sources and methods: </strong>Databases, including PubMed, Web of Science, Embase, and Cochrane, were searched by computer before August 2023 based on Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) guidelines, and reports on the efficacy and safety of camrelizumab-based treatment for NSCLC were collected, and RevMan 5.4 software was employed for meta-analysis finally.</p><p><strong>Results: </strong>Totally, 5 RCTs, 2 cohort studies, and 12 single-arm studies were included. The meta-analysis results revealed that, compared with the treatment without camrelizumab, the camrelizumab-based combination treatment considerably extended the OS (hazard ratio (HR) = 0.60, 95% confidence interval (CI): (0.44-0.82), <i>p</i> < 0.01), PFS (HR = 0.42, 95% CI: (0.28-0.63), <i>p</i> < 0.01), and event-free survival (EFS) (HR = 0.55, 95% CI: (0.44-0.68), <i>p</i> < 0.01). The median objective response rate in single-arm studies was 41% (95% CI: 28%-53%), and the disease control rate was 84% (95% CI: 78%-89%). Furthermore, in terms of the occurrence of grades 3-5 adverse events, the incidence of neutropenia was lower in the camrelizumab combination group than in the control group, while the incidence of leukopenia and rash was higher than in the combination group, and no significant difference was revealed in the incidence of other adverse events. Among single-arm studies, the incidence of grades 3-5 adverse events did not exceed 10%.</p><p><strong>Conclusion: </strong>Treatment combined with camrelizumab can effectively prolong OS, PFS, and EFS in NSCLC patients with good safety, camrelizumab combined with chemotherapy is an effective treatment option for NSCLC patients.</p>","PeriodicalId":23053,"journal":{"name":"Therapeutic Advances in Medical Oncology","volume":"16 ","pages":"17588359241284904"},"PeriodicalIF":4.3000,"publicationDate":"2024-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11457245/pdf/","citationCount":"0","resultStr":"{\"title\":\"Efficacy and safety of camrelizumab-based comprehensive treatment for non-small cell lung cancer: a systematic review and meta-analysis.\",\"authors\":\"Nuerbiyamu Maimaitiyiming, Yue Li, Yunfeng Cao, Yanwei Li\",\"doi\":\"10.1177/17588359241284904\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Many studies show that camrelizumab combination therapy can significantly improve progression-free survival (PFS) and overall survival (OS) in non-small cell lung cancer (NSCLC). However, the time of camrelizumab to market is short, and there is no systematic evaluation of camrelizumab-based comprehensive treatment of NSCLC.</p><p><strong>Objectives: </strong>To systematically evaluate the efficacy and safety of camrelizumab in comprehensively treating NSCLC.</p><p><strong>Design: </strong>A systematic review and meta-analysis.</p><p><strong>Data sources and methods: </strong>Databases, including PubMed, Web of Science, Embase, and Cochrane, were searched by computer before August 2023 based on Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) guidelines, and reports on the efficacy and safety of camrelizumab-based treatment for NSCLC were collected, and RevMan 5.4 software was employed for meta-analysis finally.</p><p><strong>Results: </strong>Totally, 5 RCTs, 2 cohort studies, and 12 single-arm studies were included. The meta-analysis results revealed that, compared with the treatment without camrelizumab, the camrelizumab-based combination treatment considerably extended the OS (hazard ratio (HR) = 0.60, 95% confidence interval (CI): (0.44-0.82), <i>p</i> < 0.01), PFS (HR = 0.42, 95% CI: (0.28-0.63), <i>p</i> < 0.01), and event-free survival (EFS) (HR = 0.55, 95% CI: (0.44-0.68), <i>p</i> < 0.01). The median objective response rate in single-arm studies was 41% (95% CI: 28%-53%), and the disease control rate was 84% (95% CI: 78%-89%). Furthermore, in terms of the occurrence of grades 3-5 adverse events, the incidence of neutropenia was lower in the camrelizumab combination group than in the control group, while the incidence of leukopenia and rash was higher than in the combination group, and no significant difference was revealed in the incidence of other adverse events. 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引用次数: 0
摘要
研究背景许多研究表明,康瑞珠单抗联合疗法可显著改善非小细胞肺癌(NSCLC)患者的无进展生存期(PFS)和总生存期(OS)。然而,康瑞珠单抗上市时间较短,目前尚未对基于康瑞珠单抗的NSCLC综合治疗进行系统评估:系统评估康瑞珠单抗综合治疗NSCLC的有效性和安全性:设计:系统综述和荟萃分析:根据系统综述和荟萃分析首选报告项目(Preferred Reporting Items for Systematic Review and Meta-Analysis,PRISMA)指南,于2023年8月前通过计算机检索PubMed、Web of Science、Embase和Cochrane等数据库,收集基于坎瑞珠单抗治疗NSCLC的疗效和安全性的相关报道,最后采用RevMan 5.4软件进行荟萃分析:结果:共纳入 5 项 RCT 研究、2 项队列研究和 12 项单臂研究。荟萃分析结果显示,与不使用坎瑞珠单抗的治疗相比,以坎瑞珠单抗为基础的联合治疗大大延长了患者的OS(危险比(HR)=0.60,95%置信区间(CI):(0.44-0.82),p p p 结论:与不使用坎瑞珠单抗的治疗相比,以坎瑞珠单抗为基础的联合治疗大大延长了患者的OS:康瑞珠单抗联合治疗可有效延长NSCLC患者的OS、PFS和EFS,且安全性良好,康瑞珠单抗联合化疗是NSCLC患者的有效治疗方案。
Efficacy and safety of camrelizumab-based comprehensive treatment for non-small cell lung cancer: a systematic review and meta-analysis.
Background: Many studies show that camrelizumab combination therapy can significantly improve progression-free survival (PFS) and overall survival (OS) in non-small cell lung cancer (NSCLC). However, the time of camrelizumab to market is short, and there is no systematic evaluation of camrelizumab-based comprehensive treatment of NSCLC.
Objectives: To systematically evaluate the efficacy and safety of camrelizumab in comprehensively treating NSCLC.
Design: A systematic review and meta-analysis.
Data sources and methods: Databases, including PubMed, Web of Science, Embase, and Cochrane, were searched by computer before August 2023 based on Preferred Reporting Items for Systematic Review and Meta-Analysis (PRISMA) guidelines, and reports on the efficacy and safety of camrelizumab-based treatment for NSCLC were collected, and RevMan 5.4 software was employed for meta-analysis finally.
Results: Totally, 5 RCTs, 2 cohort studies, and 12 single-arm studies were included. The meta-analysis results revealed that, compared with the treatment without camrelizumab, the camrelizumab-based combination treatment considerably extended the OS (hazard ratio (HR) = 0.60, 95% confidence interval (CI): (0.44-0.82), p < 0.01), PFS (HR = 0.42, 95% CI: (0.28-0.63), p < 0.01), and event-free survival (EFS) (HR = 0.55, 95% CI: (0.44-0.68), p < 0.01). The median objective response rate in single-arm studies was 41% (95% CI: 28%-53%), and the disease control rate was 84% (95% CI: 78%-89%). Furthermore, in terms of the occurrence of grades 3-5 adverse events, the incidence of neutropenia was lower in the camrelizumab combination group than in the control group, while the incidence of leukopenia and rash was higher than in the combination group, and no significant difference was revealed in the incidence of other adverse events. Among single-arm studies, the incidence of grades 3-5 adverse events did not exceed 10%.
Conclusion: Treatment combined with camrelizumab can effectively prolong OS, PFS, and EFS in NSCLC patients with good safety, camrelizumab combined with chemotherapy is an effective treatment option for NSCLC patients.
期刊介绍:
Therapeutic Advances in Medical Oncology is an open access, peer-reviewed journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of cancer. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in medical oncology, providing a forum in print and online for publishing the highest quality articles in this area. This journal is a member of the Committee on Publication Ethics (COPE).