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首页> 外文期刊>Hepatology research: the official journal of the Japan Society of Hepatology >Clinical outcome of esophageal varices after hepatic arterial infusion chemotherapy for advanced hepatocellular carcinoma with major portal vein tumor thrombus.
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Clinical outcome of esophageal varices after hepatic arterial infusion chemotherapy for advanced hepatocellular carcinoma with major portal vein tumor thrombus.

机译:肝动脉灌注化疗对晚期肝细胞癌合并主要门静脉肿瘤血栓的食管静脉曲张的临床疗效。

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摘要

Aim: To analyze the clinical outcome of esophageal varices (EV) after hepatic arterial infusion chemotherapy (HAIC) in patients with advanced hepatocellular carcinoma (HCC) and major portal vein tumor thrombus (Vp3/4). Methods: The study subjects were 45 consecutive patients who received HAIC for HCC with Vp3/4 between January 2005 and December 2009. HAIC comprised the combination therapy of intra-arterial 5-FU with interferon-alpha (5-FU/IFN) in 23 patients and low-dose cisplatin plus 5-FU (FP) in 22. Radiotherapy (RT) was also provided in 19 patients for portal vein tumor thrombosis. Aggravation rate for EV and overall survival rate were analyzed. Results: The aggravation rates for EV were 47% and 64% at 12 and 24 months, respectively. The survival rates were 47% and 33% at 12 and 24 months, respectively. The response rates to 5-FU/IFN and FP were 35% and 41%, while the disease control rates in these two groups were 57% and 50%, respectively. There were no significant differences in the objective response and disease control between 5-FU/IFN and FP. Multivariate analysis identified size of EV (F2/F3) (HR = 7.554, P = 0.006) and HCC disease control (HR = 5.948, P = 0.015) as significant and independent determinants of aggravation of EV, and HCC disease control (HR = 12.233, P < 0.001), metastasis from HCC (HR = 11.469, P = 0.001), ascites (HR = 8.825, P = 0.003) and low serum albumin (HR = 4.953, P = 0.026) as determinants of overall survival. RT for portal vein tumor thrombosis tended to reduce the aggravation rate for EV in patients with these risk factors. Conclusions: Hepatocellular carcinoma disease control was the most significant and independent factor for aggravation of EV and overall survival in HCC patients with major portal vein tumor thrombosis treated with HAIC.
机译:目的:分析晚期肝细胞癌(HCC)和主要门静脉肿瘤血栓(Vp3 / 4)患者肝动脉灌注化疗(HAIC)后食管静脉曲张(EV)的临床结果。方法:研究对象为45位连续患者,于2005年1月至2009年12月期间接受HIC联合Vp3 / 4治疗HCC。在23例患者中,HAIC联合使用了动脉内5-FU与干扰素-α(5-FU / IFN)联合治疗。患者和22例低剂量顺铂加5-FU(FP)患者中,还对19例患者进行了门静脉肿瘤血栓形成放疗(RT)。分析了EV的恶化率和总生存率。结果:在12和24个月时,EV的恶化率分别为47%和64%。 12个月和24个月的生存率分别为47%和33%。对5-FU / IFN和FP的应答率分别为35%和41%,而两组的疾病控制率分别为57%和50%。 5-FU / IFN和FP在客观反应和疾病控制方面无显着差异。多变量分析确定EV(F2 / F3)的大小(HR = 7.554,P = 0.006)和HCC疾病控制(HR = 5.948,P = 0.015)是EV和HCC疾病控制(HR = 12.233,P <0.001),肝癌的转移(HR = 11.469,P = 0.001),腹水(HR = 8.825,P = 0.003)和低血清白蛋白(HR = 4.953,P = 0.026)是总生存率的决定因素。对于具有这些危险因素的患者,门静脉肿瘤血栓形成的放疗倾向于降低EV的加重率。结论:肝细胞癌疾病的控制是HAIC治疗的主要门静脉肿瘤血栓形成的HCC患者EV恶化和总体生存的最重要和独立因素。

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