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Enhanced therapeutic efficacy of combined use of sorafenib and transcatheter arterial chemoembolization for treatment of advanced hepatocellular carcinoma

机译:索拉非尼联合经导管动脉化疗栓塞治疗晚期肝细胞癌的治疗效果增强

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Objective: Clinical trials suggest that combining transcatheter arterial chemoembolization with sorafenib in patients with advanced hepatocellular carcinoma shows a superior safety and tolerability profile. Our study aimed to retrospectively analyze the utility and prognostic factors of this combined therapy in these patients. Methods: Patients with advanced hepatocellular carcinoma, treated by transcatheter arterial chemoembolization and sorafenib subsequently, between February 2010 and September 2012 in our hospital, were retrospectively analyzed. After sorafenib treatment for 12 weeks, abdominal enhanced computed tomography or magnetic resonance imaging was used to evaluate short-term outcomes and clinical benefit rate. Overall survival and adverse events were recorded during follow-up. Univariate and multivariate analyses were used to identify relationships between baseline characteristics and overall survival. Results: Fifty-one advanced hepatocellular carcinoma patients were included. Common adverse events for sorafenib were hand-foot skin reaction, alopecia, diarrhea, anorexia and fatigue. The clinical benefit rate was 64% and the median survival time was 7.5 months. Median survival of patients with and without portal vein tumor thrombi was 6.0 months and 10.3 months (P < 0.001), respectively. Median survival of patients with cholinesterase ≥ 5000 U/l and < 5000 U/l was 10.6 months and 6.1 months (P < 0.001), respectively. Multivariate analysis identified the presence of portal vein tumor thrombi and low cholinesterase level as independent negative predictors of survival. Conclusions: Combining sorafenib and transcatheter arterial chemoembolization was safe and effective for advanced hepatocellular carcinoma patients with extrahepatic spread but without portal vein tumor thrombi. Portal vein tumor thrombi and cholinesterase level are independent predictors of prognosis following this combined therapy.
机译:目的:临床试验表明,经导管动脉化疗栓塞与索拉非尼联合治疗在晚期肝细胞癌中显示出优越的安全性和耐受性。我们的研究旨在回顾性分析这些患者联合治疗的效用和预后因素。方法:回顾性分析2010年2月至2012年9月在我院行经导管动脉化疗栓塞和索拉非尼治疗的晚期肝细胞癌患者的临床资料。索拉非尼治疗12周后,采用腹部增强计算机断层扫描或磁共振成像来评估短期结果和临床受益率。在随访期间记录了总体生存和不良事件。使用单变量和多变量分析来确定基线特征和总体生存率之间的关系。结果:纳入51例晚期肝细胞癌患者。索拉非尼的常见不良事件为手足皮肤反应,脱发,腹泻,厌食和疲劳。临床受益率为64%,中位生存时间为7.5个月。有和无门静脉肿瘤血栓的患者的中位生存期分别为6.0个月和10.3个月(P <0.001)。胆碱酯酶≥5000 U / l和<5000 U / l的患者的中位生存期分别为10.6个月和6.1个月(P <0.001)。多变量分析确定门静脉肿瘤血栓的存在和胆碱酯酶水平低是生存的独立阴性指标。结论:索拉非尼联合经导管动脉化疗栓塞治疗晚期肝细胞癌肝外扩散但无门静脉肿瘤血栓的安全性和有效性。在联合治疗后,门静脉肿瘤血栓和胆碱酯酶水平是预后的独立预测因子。

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