Miyaguchi Shingo, Watanabe Tetsu, Takahashi Hiyori, Nakamura Mitsuyasu, Saito Hidetsugu, Ishii Hiromasa
Department of Internal Medicine, Tokyo Metropolitan Otsuka Hospital, Minami-Otsuka 2-8-1, Toshima-ku, Tokyo, Japan.
Hepatogastroenterology. 2002 May-Jun;49(45):724-9.
BACKGROUND/AIMS: Interferon-alfa is widely used for the treatment of chronic hepatitis C, and has been thought to have a preventive effect on the development of hepatocellular carcinoma. Hepatocellular carcinoma develops from chronic liver diseases such as chronic hepatitis C or liver cirrhosis. We studied the effect of interferon for liver cirrhosis with hepatocellular carcinoma after treating hepatocellular carcinoma itself.
To evaluate the preventive effect of this drug on local recurrence and/or new development of primary tumor after clearance of hepatitis C virus, 46 patients with hepatocellular carcinoma with low HCV-RNA level were randomized to receive recombinant interferon-alfa 2b (n = 22) or not (n = 24) after being treated by transcatheter arterial chemoembolization and percutaneous ethanol injection therapy. In the interferon-treated group, patients received 3 million international units of interferon-alfa 2b intramuscularly three times a week for 4 months. In both groups, transcatheter arterial chemoembolization followed by percutaneous ethanol injection therapy was performed as an initial treatment and these therapies were repeated every 4-6 months. Serum HCV-RNA levels of all 46 patients were under 0.5 Meq/mL by branched DNA probe assay.
In the interferon-treated group, 11 of the 22 (50%) patients were HCV-RNA negative at the 6 months after completing the course of interferon therapy. HCV-RNA was undetectable during the observation period in 2 of the 24 (9.5%) patients in the untreated group. The survival rate in the interferon-treated group was significantly higher than that in the untreated group (P = 0.01 by the log-rank test). Though there was no significant difference in the incidence of local recurrence in both groups, the incidence of secondary hepatocellular carcinoma was significantly lower in the interferon-treated group than that in the untreated group. Cox proportional hazards regression analysis validated interferon treatment as an independent predictor of hepatocellular carcinoma prognosis.
We concluded that, if HCV-RNA level is low, interferon may be a therapy of choice in combination with transcatheter arterial chemoembolization and percutaneous ethanol injection therapy for the treatment of hepatocellular carcinoma.
背景/目的:干扰素-α被广泛用于治疗慢性丙型肝炎,并且一直被认为对肝细胞癌的发生具有预防作用。肝细胞癌由慢性丙型肝炎或肝硬化等慢性肝病发展而来。我们研究了在治疗肝细胞癌本身之后,干扰素对伴有肝细胞癌的肝硬化的影响。
为了评估该药物对丙型肝炎病毒清除后原发性肿瘤局部复发和/或新发生的预防作用,46例HCV-RNA水平较低的肝细胞癌患者在接受经动脉化疗栓塞和经皮乙醇注射治疗后,被随机分为接受重组干扰素-α 2b治疗组(n = 22)和未接受治疗组(n = 24)。在干扰素治疗组中,患者每周三次肌肉注射300万国际单位的干扰素-α 2b,共4个月。两组均以经动脉化疗栓塞继以经皮乙醇注射治疗作为初始治疗,并且这些治疗每4 - 6个月重复进行一次。通过分支DNA探针分析,所有46例患者的血清HCV-RNA水平均低于0.5 Meq/mL。
在干扰素治疗组中,22例患者中有11例(50%)在完成干扰素治疗疗程后的6个月时HCV-RNA呈阴性。在未治疗组的24例患者中,有2例(9.5%)在观察期内HCV-RNA检测不到。干扰素治疗组的生存率显著高于未治疗组(对数秩检验P = 0.01)。虽然两组局部复发的发生率没有显著差异,但干扰素治疗组继发性肝细胞癌的发生率显著低于未治疗组。Cox比例风险回归分析证实干扰素治疗是肝细胞癌预后的独立预测因素。
我们得出结论,如果HCV-RNA水平较低,干扰素可能是与经动脉化疗栓塞和经皮乙醇注射治疗联合用于治疗肝细胞癌的一种选择疗法。