首页> 美国卫生研究院文献>World Journal of Gastroenterology >Improved survival for hepatocellular carcinoma with portal vein tumor thrombosis treated by intra-arterial chemotherapy combining etoposide carboplatin epirubicin and pharmacokinetic modulating chemotherapy by 5-FU and enteric-coated tegafur/uracil: A pilot study
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Improved survival for hepatocellular carcinoma with portal vein tumor thrombosis treated by intra-arterial chemotherapy combining etoposide carboplatin epirubicin and pharmacokinetic modulating chemotherapy by 5-FU and enteric-coated tegafur/uracil: A pilot study

机译:动脉内化疗结合依托泊苷卡铂表柔比星和5-FU肠溶替加氟/尿嘧啶的药代动力学调节化疗治疗肝细胞癌合并门静脉肿瘤血栓形成的生存率:一项先导研究

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摘要

AIM: To investigate the poor prognosis of HCC with PVTT, we evaluated the efficacy by a new combination chemotherapy for advanced hepatocellular carcinoma (HCC) with portal vein tumor thrombus (PVTT).METHODS: From 2002 to 2007, a total of 10 consecutive patients with Stage IVA HCC accompanied by PVTT were studied prospectively to examine the efficacy of treatment by intra-arterial infusion of a chemotherapeutic agents consisting of etoposide, carboplatin, epirubicin and pharmacokinetic modulating chemotherapy by 5-FU and enteric-coated tegafur/uracil.RESULTS: The mean course of chemotherapy was 14.4 (range, 9-21) mo. One patient showed complete response (CR) with disappearance of HCC and PVTT after treatment, and the two patients showed partial response (PR), response rate (CR + PR/All cases 30%). The median survival time after the therapy was 457.2 d. The one-year survival rate was 70%. Adverse reactions were tolerable.CONCLUSION: Although the prognosis of most patients with Stage IVA HCC by PVTT is poor, our combination chemotherapy may induces long-term survival and is an effective treatment and produced anti-tumor activity with tolerable adverse effects in patients for advanced Stage IVA HCC accompanied by PVTT.
机译:目的:为了研究PVTT对肝癌的不良预后,我们评估了一种新的联合化疗对晚期肝细胞癌(HCC)合并门静脉肿瘤血栓(PVTT)的疗效。方法:从2002年至2007年,共10例患者前瞻性研究了IVA期HCC伴PVTT的患者,以研究动脉内输注由5-FU和肠溶性替加氟/尿嘧啶组成的化疗药物(包括依托泊苷,卡铂,表柔比星和药代动力学调节化疗)的治疗效果。平均化疗疗程为14.4(范围:9-21)mo。一名患者在治疗后表现出完全缓解(CR),伴有肝癌和PVTT消失,两名患者表现出部分缓解(PR),缓解率(CR + PR /所有病例均为30%)。治疗后中位生存时间为457.2 d。一年生存率为70%。结论:尽管大多数PVTT治疗的IVA期肝癌患者的预后较差,但我们的联合化疗可能诱导长期生存,是一种有效的治疗方法,并产生抗肿瘤活性,对晚期患者可耐受的不良反应IVVA HCC阶段伴随PVTT。

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