Department of Oncology, IRCCS S. Maugeri Foundation, 10 Maugeri Street, 27100 Pavia, Italy.
Anticancer Res. 2011 Nov;31(11):3927-33.
Sorafenib is the only therapy approved for advanced hepatocellular carcinoma no longer eligible for transcatheter arterial chemoembolization. Hepatic intra-arterial chemotherapy has been shown to be an effective and safe therapy for advanced hepatocellular carcinoma. Cetuximab has been administered intravenously to patients with advanced hepatocellular carcinoma, showing encouraging results in terms of its safety and toxicity profile.
Our purpose was to evaluate the safety and feasibility of hepatic arterial chemotherapy with cetuximab, cisplatin and 5-fluoruracil for patients with advanced hepatocellular carcinoma, not responsive or not eligible for sorafenib therapy.
From January 2010 to January 2011, 12 patients received a 2-day course of chemotherapy consisting of repeated daily hepatic arterial administration of 20 mg of cisplatin as 2-h infusion, 5-fluorouracil at 500 mg/m(2) as 5-h infusion and cetuximab 500 mg/m(2) as 12-h infusion. Cycles were repeated every 14 days.
After a mean of four months of therapy, computed tomography revealed five partial responses, five cases of stable disease and two of progressive disease. The toxicity profile was favourable, with no G4 gastrointestinal, hematologic or skin side-effects, or severe deterioration of liver function.
Hepatic intra-arterial chemotherapy with cetuximab is a safe and feasible treatment for advanced hepatocellular carcinoma, with promising results in patients with initial poor prognosis.
索拉非尼是唯一被批准用于不再适合经导管动脉化疗栓塞的晚期肝细胞癌的治疗药物。肝动脉内化疗已被证明是一种有效且安全的治疗晚期肝细胞癌的方法。西妥昔单抗已被静脉给药用于治疗晚期肝细胞癌,其安全性和毒性特征显示出令人鼓舞的结果。
我们的目的是评估西妥昔单抗、顺铂和 5-氟尿嘧啶联合肝动脉化疗治疗对索拉非尼治疗无效或不适合索拉非尼治疗的晚期肝细胞癌患者的安全性和可行性。
从 2010 年 1 月至 2011 年 1 月,12 例患者接受了为期 2 天的化疗方案,包括每天重复肝动脉内输注 20mg 顺铂作为 2 小时输注,5-氟尿嘧啶 500mg/m²作为 5 小时输注,西妥昔单抗 500mg/m²作为 12 小时输注。周期每 14 天重复一次。
在平均 4 个月的治疗后,计算机断层扫描显示 5 例部分缓解,5 例疾病稳定,2 例疾病进展。毒性特征良好,无 G4 胃肠道、血液学或皮肤副作用,或肝功能严重恶化。
西妥昔单抗肝动脉内化疗是一种安全且可行的治疗晚期肝细胞癌的方法,对初始预后较差的患者有较好的疗效。