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The Efficacy and Toxicity of Gefitinib in Treating Non-small Cell Lung Cancer: A Meta-analysis of 19 Randomized Clinical Trials

机译:吉非替尼治疗非小细胞肺癌的疗效和毒性:19项随机临床试验的荟萃分析

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摘要

>Background: This meta-analysis evaluated the efficacy and toxicity of gefitinib with other commonly used drugs in different treatment settings and epidermal growth factor receptor (EGFR) mutation status.>Methods: Nineteen randomize clinical trials (RCTs) of 6,554 patients with NSCLC were pooled in this meta-analysis by random-effects or fixed-effects model, whichever is proper.>Results: In first-line therapy, gefitinib showed higher odds than chemotherapy (OR = 2.19, 95% CI: 1.20-4.01), but less than other targeted therapies (OR = 0.58, 95% CI: 0.38-0.88). As non-first-line therapy, the overall survival (OS) and progression-free survival (PFS) were similar between gefitinib and controls (HR = 1.00, 95% CI: 0.93-1.08; HR = 0.91, 95% CI: 0.72-1.15), respectively. With the regard to toxicity, the incidences of dry skin, rash and pruritus were higher in gefitinib compared with controls, while gefitinib significantly reduced the incidence of hematologic toxicity.>Conclusion: Gefitinib might be more efficient than chemotherapy, but less efficient than other targeted therapies in ORR, especially in EGFR mutation-positive patients. Gefitinib can decrease the odds of hematologic toxicity compared to controls. Future studies, especially those with EGFR mutation-positive patients, will be needed to confirm our findings.
机译:>背景:这项荟萃分析评估了吉非替尼与其他常用药物在不同治疗环境和表皮生长因子受体(EGFR)突变状态下的疗效和毒性。>方法: 19在这项荟萃分析中,采用随机效应或固定效应模型(以适当者为准)汇总了6,554例NSCLC患者的随机临床试验(RCT)。>结果:在一线治疗中,吉非替尼显示出更高的疗效比化疗的几率高(OR = 2.19,95%CI:1.20-4.01),但比其他靶向疗法要低(OR = 0.58,95%CI:0.38-0.88)。作为非一线疗法,吉非替尼和对照组的总生存期(OS)和无进展生存期(PFS)相似(HR = 1.00,95%CI:0.93-1.08; HR = 0.91,95%CI:0.72 -1.15)。在毒性方面,吉非替尼比对照组的皮肤干燥,皮疹和瘙痒的发生率更高,而吉非替尼显着降低了血液毒性的发生率。>结论:吉非替尼可能比化疗更有效,但在ORR中效果不如其他靶向疗法,尤其是在EGFR突变阳性患者中。与对照组相比,吉非替尼可降低血液学毒性的几率。需要进一步的研究,特别是那些EGFR突变阳性患者的研究,以证实我们的发现。

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