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Results of a randomized and controlled clinical trial evaluating the efficacy and safety of combination therapy with Endostar and S-1 combined with oxaliplatin in advanced gastric cancer

机译:评估Endostar和S-1联合奥沙利铂联合治疗晚期胃癌的有效性和安全性的随机对照临床试验结果

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Objectives: We aimed to evaluate the efficacy and safety of combination therapy of Endostar (recombinant human endostatin) and S-1 combined with oxaliplatin (SOX) in patients with advanced gastric cancer.Methods: In this randomized, controlled trial, 165 late-stage gastric cancer patients were assigned to the experimental arm with Endostar in combination with SOX (80 patients) and the control arm with SOX alone (85 patients). The end points of this study included progression-free survival, response rate, and disease-control rate.Results: There was no statistically significant difference in response rate between the experimental arm and the control arm (53.8% vs 42.4%, P=0.188). The difference in disease-control rate was also statistically insignificant between the two arms (85.0% vs 72.9%, P=0.188). Progression-free survival in the experimental arm was significantly higher than that in the control arm (15.0 months vs 12.0 months, P=0.0001). Common adverse events included immunosuppression, gastrointestinal distress, and neuropathy. There was no statistical difference in the incidences of adverse events.Conclusion: Combination therapy of Endostar and SOX provides therapeutic benefits to advanced gastric cancer patients, with tolerable adverse effects.
机译:目的:我们旨在评估Endostar(重组人内皮抑素)和S-1联合奥沙利铂(SOX)在晚期胃癌患者中联合治疗的有效性和安全性。方法:该随机对照试验在165个晚期阶段胃癌患者被分配为Endostar联合SOX的实验组(80例)和单独使用SOX的对照组(85例)。本研究的终点包括无进展生存期,缓解率和疾病控制率。结果:实验组与对照组之间的缓解率无统计学差异(53.8%vs 42.4%,P = 0.188) )。两组之间的疾病控制率差异也无统计学意义(85.0%对72.9%,P = 0.188)。实验组的无进展生存期显着高于对照组(15.0个月对12.0个月,P = 0.0001)。常见的不良事件包括免疫抑制,胃肠道不适和神经病。结论:Endostar和SOX联合治疗对晚期胃癌患者具有治疗效果,且不良反应可耐受。

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