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使用顺铂、5-氟尿嘧啶和亚叶酸钙对晚期肝细胞癌患者进行新型动脉灌注化疗。

Novel arterial infusion chemotherapy using cisplatin, 5-fluorouracil, and leucovorin for patients with advanced hepatocellular carcinoma.

作者信息

Yamasaki Takahiro, Kurokawa Fumie, Shirahashi Hitoshi, Kusano Noriyoshi, Hironaka Kouji, Masuhara Masaaki, Okita Kiwamu

机构信息

Department of Gastroenterology and Hepatology, Yamaguchi University School of Medicine, 1-1-1 Minamikogushi, Ube, 755-8505, Yamaguchi, Japan

出版信息

Hepatol Res. 2002 May;23(1):7-17. doi: 10.1016/s1386-6346(01)00163-2.

Abstract

Advanced hepatocelluar carcinoma (HCC) has a poor prognosis. In this study, the authors evaluated the efficacy of chemotherapy using cisplatin (CDDP), 5-fluorouracil (5-FU), and leucovorin (LV), comparing our regimen with chemotherapy using CDDP and 5-FU. Nineteen patients with advanced HCC were treated by arterial infusion of a chemotherapeutic agent via a subcutaneously implanted injection port. In Group A (n=9), one course of chemotherapy consisted of the daily administration of CDDP (10 mg/1 h, on 5 days) and LV (12 mg/10 min, on 5 days) followed by 5-FU (250 mg/5 h, on 5 days). In Group B (n=10), except for the administration of LV, the same regimen was employed. This course was repeated each week for 4 weeks. In Group A, two patients showed a complete response (CR), and the other three showed a partial response (PR). In Group B, two patients showed PR. The response rate (CR+PR/all cases) in Group A was significantly higher than that in Group B (56 vs. 20%; P=0.022). The 1- and 2-year survival rates of Group A (66.7, 44.4%) were significantly higher than those of Group B (10, 0%) (P=0.033). These results suggest that our regimen may be useful in treating patients with advanced HCC.

摘要

晚期肝细胞癌(HCC)预后较差。在本研究中,作者评估了使用顺铂(CDDP)、5-氟尿嘧啶(5-FU)和亚叶酸钙(LV)进行化疗的疗效,并将我们的方案与使用CDDP和5-FU的化疗方案进行比较。19例晚期HCC患者通过经皮下植入的注射端口进行动脉内化疗药物灌注治疗。A组(n = 9),一个化疗疗程包括每日给予CDDP(10 mg/1小时,共5天)和LV(12 mg/10分钟,共5天),随后给予5-FU(250 mg/5小时,共5天)。B组(n = 10),除不给予LV外,采用相同方案。该疗程每周重复1次,共4周。A组中,2例患者完全缓解(CR),另外3例部分缓解(PR)。B组中,2例患者PR。A组的缓解率(CR + PR/所有病例)显著高于B组(56%对20%;P = 0.022)。A组的1年和2年生存率(66.7%,44.4%)显著高于B组(10%,0%)(P = 0.033)。这些结果表明,我们的方案可能对治疗晚期HCC患者有用。

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