首页> 美国卫生研究院文献>Journal of Translational Internal Medicine >Protracted Inhibition of Vascular Endothelial Growth Factor Signaling Improves Survival in Metastatic Colorectal Cancer: A Systematic Review
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Protracted Inhibition of Vascular Endothelial Growth Factor Signaling Improves Survival in Metastatic Colorectal Cancer: A Systematic Review

机译:血管内皮生长因子信号的长期抑制可改善转移性结直肠癌的生存:系统评价

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摘要

Clinical data suggest that beyond-progression, the blockade of angiogenesis is associated with improved survivals in colorectal cancer. We conducted a systematic review to investigate the therapeutic effects of antiangiogenic drugs administered as later lines of treatment in patients already progressed to a previous anti-VEGF based treatment. An extensive literature search was conducted. Hazard ratios (HR) for progression (PFS) and death (OS) were extracted. An inverse-variance meta-analysis model was implemented. 6 randomized controlled trials were retrieved, including 3407 patients, treated with different antiangiogenic drugs. All of them had progressed during or after a previous line of treatment with bevacizumab. Overall, both PFS (HR=0.63, P <0.001) and OS (HR=0.81, P < 0.001) were significantly increased with the use of antiangiogenic drug. No heterogeneity was observed despite different drugs. Protracted inhibition of the VEGF pathway is associated with a significant improvement of both PFS and OS, independently from the antiangiogenic agent used.
机译:临床数据表明,血管生成的过度发展与结直肠癌的生存改善有关。我们进行了系统的综述,以调查抗血管生成药物的治疗效果,因为该药物在已经发展到先前基于抗VEGF的治疗中的患者的后续治疗中得到了应用。进行了广泛的文献检索。提取进展风险(HR)和死亡风险(OS)。实施了反方差荟萃分析模型。检索了6项随机对照试验,包括3407例接受不同抗血管生成药物治疗的患者。所有患者在接受贝伐单抗前一线治疗期间或之后均已进展。总体而言,使用抗血管生成药物后,PFS(HR = 0.63,P <0.001)和OS(HR = 0.81,P <0.001)均显着增加。尽管药物不同,但未观察到异质性。长期抑制VEGF通路与PFS和OS的显着改善相关,而与所使用的抗血管生成剂无关。

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