Miura K, Nakao N, Yoshimoto A, Yamano T, Inoue J, Takayasu Y
Dept. of Radiology, Hyogo College of Medicine.
Gan To Kagaku Ryoho. 1998 Feb;25 Suppl 1:51-5.
Twenty-four patients were treated with arterial infusion of SMANCS dissolved in Lipiodol. Twenty of these patients had HCC with the main trunks of portal vein occluded by tumor, and four patients had severe cirrhosis and multiple HCC. The actual dose of SMANCS administered each patient ranged from 4 to 6 mg. Side effects occurred in 50%. Severe side effects such as shock and shivering-chilliness were observed in 18%. The differences between the values of hepatic functional serum indexes obtained before and after treatment with SMANCS were small and transient. With regard to the therapeutic response of the arterial infusion of SMANCS, the mean survival time was approximately 2.8 months. It was suggested that the more effective administration of SMANCS was combination of the arterial infusion of SMANCS-Lipiodol with TAE at the level of the right hepatic artery of left hepatic artery for multiple HCC.
24例患者接受了溶解于碘油的丝裂霉素(SMANCS)动脉灌注治疗。其中20例患者为肝癌伴门静脉主干被肿瘤阻塞,4例患者为严重肝硬化伴多发性肝癌。每位患者的SMANCS实际给药剂量为4至6毫克。50%的患者出现了副作用。18%的患者出现了严重副作用,如休克和寒战。SMANCS治疗前后获得的肝功能血清指标值差异较小且短暂。关于SMANCS动脉灌注的治疗反应,平均生存时间约为2.8个月。对于多发性肝癌,建议更有效的SMANCS给药方法是在肝右动脉或肝左动脉水平将SMANCS - 碘油动脉灌注与经动脉化疗栓塞(TAE)联合使用。