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首页> 外文期刊>International Journal of Clinical and Experimental Medicine >The efficacy and safety of adding bevacizumab to cetuximab- or panitumumab-based therapy in the treatment of patients with metastatic colorectal cancer (mCRC): a meta-analysis from randomized control trials
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The efficacy and safety of adding bevacizumab to cetuximab- or panitumumab-based therapy in the treatment of patients with metastatic colorectal cancer (mCRC): a meta-analysis from randomized control trials

机译:在基于西妥昔单抗或帕尼单抗的治疗中添加贝伐单抗治疗转移性结直肠癌(mCRC)的有效性和安全性:一项来自随机对照试验的荟萃分析

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Objective: To estimate the efficacy and safety of adding bevacizumab to cetuximab- or panitumumab-based therapy in the treatment of patients with metastatic colorectal cancer (mCRC), using a meta-analysis of randomized controlled trials. Methods: A literature search for randomized clinical trials (RCTs) was performed through Pubmed, Embase, and Web of Science (up to May 22, 2014). The outcome measures were progression-free survival (PFS), overall survival (OS), objective response rate (ORR), and adverse events. Two investigators identified eligible studies and extracted data independently. The quality of the included studies was assessed by the Jadad score. Hazard ratios (HR), risk ratio (RR), and 95% confidence intervals (Cls) were calculated and pooled. Results: A total of 4 RCTs with 2069 patients were included in this meta-analysis. The addition of bevacizumab to cetuximab- or panitumumab-based therapy did not significantly prolonged PFS, when compared with antibody alone. The subgroup analysis of adding bevacizumab to cetuximab-based therapy also suggested no significant benefit in PFS or in OS. Patients who received the combined therapy did not have a higher ORR (RR = 0.98, 95% CI: 0.89-1.07; P = 0.608). The incidence of grade 3/4 adverse events was not significantly higher in the bevacizumab and cetuximab/panitumumab group. Conclusion: The addition of bevacizumab to cetuximab- or panitumumab-based therapy did not improve PFS and OS resulting in better ORR. Thus, the combined therapy of bevacizumab with cetuximab or panitumumab is not recommended for the treatment of mCRC. However, larger scale RCTs are needed to confirm these findings.
机译:目的:通过一项随机对照试验的荟萃分析,评估在基于西妥昔单抗或帕尼单抗的治疗中加入贝伐单抗治疗转移性结直肠癌(mCRC)的有效性和安全性。方法:通过Pubmed,Embase和Web of Science(截至2014年5月22日)对随机临床试验(RCT)进行文献检索。结果指标为无进展生存期(PFS),总生存期(OS),客观缓解率(ORR)和不良事件。两名研究人员确定了合格的研究并独立提取了数据。通过Jadad评分评估纳入研究的质量。计算并汇总了危险比(HR),风险比(RR)和95%置信区间(Cls)。结果:这项荟萃分析共纳入了4项RCT,涉及2069名患者。与单独的抗体相比,在以西妥昔单抗或帕尼单抗为基础的治疗中添加贝伐单抗不会显着延长PFS。在以西妥昔单抗为基础的治疗中添加贝伐单抗的亚组分析也表明,在PFS或OS中无明显益处。接受联合治疗的患者没有较高的ORR(RR = 0.98,95%CI:0.89-1.07; P = 0.608)。在贝伐单抗和西妥昔单抗/帕尼单抗组中,3/4级不良事件的发生率没有明显升高。结论:在以西妥昔单抗或帕尼单抗为基础的治疗中加入贝伐单抗不能改善PFS和OS,从而改善ORR。因此,不建议将贝伐单抗与西妥昔单抗或帕尼单抗联合治疗mCRC。但是,需要更大规模的RCT来证实这些发现。

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