Department of Interventional Radiology, Beijing 302 Hospital, Beijing.
Research Center for Biological Therapy, Beijing 302 Hospital, Beijing, China.
Jpn J Clin Oncol. 2014 Aug;44(8):711-7. doi: 10.1093/jjco/hyu068. Epub 2014 May 22.
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.
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.
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.
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.
临床试验表明,在晚期肝细胞癌患者中,经导管动脉化疗栓塞联合索拉非尼治疗具有更好的安全性和耐受性。本研究旨在回顾性分析该联合治疗在这些患者中的应用及预后因素。
回顾性分析 2010 年 2 月至 2012 年 9 月我院收治的经导管动脉化疗栓塞联合索拉非尼治疗的晚期肝细胞癌患者。索拉非尼治疗 12 周后,采用腹部增强 CT 或磁共振成像评估近期疗效和临床获益率。随访期间记录总生存期和不良事件。采用单因素和多因素分析确定基线特征与总生存期的关系。
共纳入 51 例晚期肝细胞癌患者。索拉非尼常见的不良反应有手足皮肤反应、脱发、腹泻、厌食和乏力。临床获益率为 64%,中位总生存期为 7.5 个月。有门静脉癌栓和无门静脉癌栓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 的患者中位生存期分别为 10.6 个月和 6.1 个月(P<0.001)。多因素分析发现门静脉癌栓和低胆碱酯酶水平是生存的独立负相关因素。
对于有肝外转移但无门静脉癌栓的晚期肝细胞癌患者,索拉非尼联合经导管动脉化疗栓塞治疗是安全有效的。门静脉癌栓和胆碱酯酶水平是该联合治疗后预后的独立预测因素。