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首页> 外文期刊>Anticancer Research: International Journal of Cancer Research and Treatment >Sorafenib vs. Lenvatinib as First-line Therapy for Advanced Hepatocellular Carcinoma With Portal Vein Tumor Thrombosis
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Sorafenib vs. Lenvatinib as First-line Therapy for Advanced Hepatocellular Carcinoma With Portal Vein Tumor Thrombosis

机译:Sorafenib对Lenvatinib作为高级肝细胞癌与门静脉肿瘤血栓形成的一线治疗

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Background/Aim: We aimed to compare the outcomes between sorafenib and lenvatinib as first-line therapy for advanced hepatocellular carcinoma (HCC) with major portal vein tumor thrombosis (Vp3/4). Patients and Methods: This retrospective study enrolled 41 HCC patients with Vp3/4 and Child-Pugh A. Results: The outcomes in the lenvatinib group (n=13) were significantly better than those in the sorafenib group (n=28) [best objective response rate according to the modified Response Evaluation Criteria in Solid Tumors: 53.8% vs. 14.3%; p=0.0193, best disease control rate: 92.3% vs. 35.7%; p=0.0008, median overall survival (OS): not reached vs. 187 days; p=0.0040, respectively]. Lenvatinib treatment was the only significant predictor of better OS and time to tumor progression. No patient needed to discontinue lenvatinib treatment due to drug-related adverse events. Conclusion: Compared with sorafenib, lenvatinib treatment for advanced HCC with Vp3/4 may lead to more favorable outcomes.
机译:背景/目的:我们的旨在将索拉非尼和Lenvatinib与主要门静脉肿瘤血栓形成(VP3 / 4)的先进肝细胞癌(HCC)的一线治疗进行比较。 患者和方法:该回顾性研究载有41名HCC患者VP3 / 4和Child-Pugh A.结果:Lenvatinib组(N = 13)的结果明显优于Sorafenib组(N = 28)的结果(n = 28) 根据固体肿瘤的改性响应评估标准的客观反应率:53.8%vs.14.3%; P = 0.0193,最佳疾病控制率:92.3%与35.7%; p = 0.0008,中位数整体生存(OS):未达到与187天; P = 0.0040,分别为0.0040。 Lenvatinib治疗是较好的OS和肿瘤进展时间的唯一重要预测因子。 由于药物相关的不良事件,没有患者停止伦紫红蛋白治疗。 结论:与索拉非尼(Sorafenib)相比,Lenvatinib与VP3 / 4的先进HCC治疗可能导致更有利的结果。

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