Cui Han-zhi, Dai Guang-hai, Shi Yan, Chen Li
Department of Oncology, No. 309 Hospital of People's Liberation Army, Beijing China.
Hepatogastroenterology. 2013 Mar-Apr;60(122):305-10. doi: 10.5754/hge12552.
BACKGROUND/AIMS: To evaluate the effectiveness and safety of sorafenib combined with transarterial chemoembolization (TACE) in patients with advanced primary hepatocellular carcinoma.
A retrospective analysis of 65 patients with advanced primary hepatocellular carcinoma who had been administered sorafenib for more than one month and treated by TACE was performed. The tumor response was evaluated according to the response evaluation criteria in solid tumors and any side effects were recorded.
Twelve patients entered a partial remission, 42 entered a stable condition, and the disease progressed in 11 patients. The disease control and objective regression rates were 83.1% and 18.5%, respectively. The one-year survival rate was 63.1%. Among the cases, the median overall survival time was 17 months, and the median time to progression was 9 months. The overall side effects rate was 78.5% and most were relieved after treatment.
Sorafenib combined with TACE is a safe and effective treatment of advanced primary hepatocellular carcinoma.
背景/目的:评估索拉非尼联合经动脉化疗栓塞术(TACE)治疗晚期原发性肝细胞癌患者的有效性和安全性。
对65例接受索拉非尼治疗超过1个月并接受TACE治疗的晚期原发性肝细胞癌患者进行回顾性分析。根据实体瘤疗效评价标准评估肿瘤反应,并记录任何副作用。
12例患者部分缓解,42例病情稳定,11例病情进展。疾病控制率和客观缓解率分别为83.1%和18.5%。一年生存率为63.1%。其中,中位总生存时间为17个月,中位疾病进展时间为9个月。总副作用发生率为78.5%,大多数在治疗后缓解。
索拉非尼联合TACE是治疗晚期原发性肝细胞癌的一种安全有效的方法。