Okusaka Takuji, Okada Shuichi, Nakanishi Toshio, Fujiyama Shigetoshi, Kubo Yasuhiko
Hepatobiliary and Pancreatic Oncology Division, National Cancer Center Hospital, Tokyo, Japan.
Invest New Drugs. 2004 Apr;22(2):169-76. doi: 10.1023/B:DRUG.0000011793.72775.d1.
SM-11355, a lipophilic platinum derivative, is a novel intra-arterial chemotherapeutic agent for hepatocellular carcinoma (HCC). A phase II study of SM-11355 was conducted to evaluate the antitumor activities and the toxicity in chemotherapy-naive patients with HCC. Sixteen patients were treated with transcatheter arterial injection of SM-11355-lipiodol emulsion (20-120 mg/body). The responses were evaluated by computed tomography 3 months after treatment. Complete response (CR) was defined as disappearance or 100% necrosis of all tumors, and lipiodol accumulation in tumors was regarded as indicating necrosis. Nine patients achieved CR (56%; 95% confidence interval, 29.9-80.2%). The grade 3 toxicities were neutropenia (19%), total bilirubin elevation (19%), AST elevation (44%), and ALT elevation (19%). None of the patients showed grade 4 toxicities or episodes of renal dysfunction. Other common adverse effects were eosinophilia (100%) and pyrexia (94%). Intra-arterial chemotherapy with SM-11355, which was well tolerated, showed promising antitumor activity in patients with HCC.
SM - 11355是一种亲脂性铂衍生物,是一种用于治疗肝细胞癌(HCC)的新型动脉内化疗药物。开展了一项关于SM - 11355的II期研究,以评估初治HCC患者的抗肿瘤活性和毒性。16例患者接受了经导管动脉注射SM - 11355 - 碘油乳剂(20 - 120mg/体)治疗。治疗3个月后通过计算机断层扫描评估反应。完全缓解(CR)定义为所有肿瘤消失或100%坏死,肿瘤内碘油积聚被视为提示坏死。9例患者达到CR(56%;95%置信区间,29.9 - 80.2%)。3级毒性包括中性粒细胞减少(19%)、总胆红素升高(19%)、谷草转氨酶升高(44%)和谷丙转氨酶升高(19%)。无患者出现4级毒性或肾功能不全发作。其他常见不良反应为嗜酸性粒细胞增多(100%)和发热(94%)。SM - 11355动脉内化疗耐受性良好,在HCC患者中显示出有前景的抗肿瘤活性。