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首页> 外文期刊>Lung cancer: Journal of the International Association for the Study of Lung Cancer >Chemotherapy with cetuximab or chemotherapy alone for untreated advanced non-small-cell lung cancer: a systematic review and meta-analysis.
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Chemotherapy with cetuximab or chemotherapy alone for untreated advanced non-small-cell lung cancer: a systematic review and meta-analysis.

机译:未经西妥昔单抗化疗或单独化疗治疗未治疗的晚期非小细胞肺癌:系统评价和荟萃分析。

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PURPOSE: To compare the efficacy and toxicities of chemotherapy plus cetuximab (Erbitux, E; E-chemo) with chemotherapy alone (chemo alone) in patients with previously untreated advanced non-small-cell lung cancer (NSCLC). The primary endpoint was overall survival; the secondary endpoints were progression-free survival, overall response rate, one-year survival and safety. METHODS: The PubMed database, the Cochrane Library, conference proceedings, database of ongoing trials and references of published trials and reviews were screened. Two reviewers independently assessed the quality of the trials and extracted data. The hazard ratios (HRs) for overall survival and progression-free survival, relative risks (RRs) for overall response rate and one-year survival, and odds ratios (ORs) for the different types of toxicity were pooled using STATA SE10.1 package. RESULTS: Four trials involving 2018 patients with previously untreated NSCLC were ultimately analyzed. The pooled HR for overall survival (HR, 0.87; 95%CI, 0.79-0.96; p=0.004) was in favor of E-chemo, which also gave rise to a higher overall response rate (RR, 1.19; 95%CI, 1.04-1.37; p=0.013). The analysis failed to show benefit of E-chemo in progression-free survival (HR, 0.91; 95%CI, 0.83-1.00; p=0.06) and one-year survival (RR, 1.10; 95%CI, 0.98-1.26; p=0.172). E-chemo indeed caused more grade 3/4 rash and infusion reaction (OR, 43.86; 95%CI, 12.46-154.44; p=0.000; OR, 3.69; 95%CI, 1.89-7.25; p=0.000; respectively). CONCLUSION: Our data showed that the addition of cetuximab to chemotherapy would improve overall survival and overall response rate. It may provide new option for clinical treatment for untreated advanced non-small-cell lung cancer. The side effects of E-chemo are predictable and manageable.
机译:目的:比较化疗加西妥昔单抗(Erbitux,E; E-chemo)与单独化疗(单独化疗)对先前未治疗的晚期非小细胞肺癌(NSCLC)患者的疗效和毒性。主要终点是总体生存率。次要终点为无进展生存期,总体缓解率,一年生存期和安全性。方法:筛选PubMed数据库,Cochrane图书馆,会议记录,进行中的试验数据库以及已发表试验和评论的参考文献。两名审稿人独立评估了试验的质量并提取了数据。使用STATA SE10.1软件包汇总了总体生存率和无进展生存率的危险比(HRs),总体缓解率和一年生存率的相对风险(RRs)以及不同类型毒性的比值比(OR)。 。结果:最终分析了四项涉及2018年先前未经治疗的NSCLC患者的试验。合并的总生存期HR(HR,0.87; 95%CI,0.79-0.96; p = 0.004)有利于E-chemo,也带来了更高的总体缓解率(RR,1.19; 95%CI, 1.04-1.37; p = 0.013)。该分析未能显示出E-chemo对无进展生存期(HR,0.91; 95%CI,0.83-1.00; p = 0.06)和一年生存期(RR,1.10; 95%CI,0.98-1.26; 10%)的益处。 p = 0.172)。电子化学确实确实引起了更多的3/4级皮疹和输注反应(OR,43.86; 95%CI,12.46-154.44; p = 0.000; OR,3.69; 95%CI,1.89-7.25; p = 0.000;)。结论:我们的数据表明,在化疗中加入西妥昔单抗可改善总生存期和总缓解率。它可能为未经治疗的晚期非小细胞肺癌的临床治疗提供新的选择。 E-chemo的副作用是可预测和可管理的。

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