Li Yong, Huang Jian-wen, Lu Li-gong, Shao Pei-jian, Hu Bao-shan, Huang Guo-min, Wei Zhao-guang, Zhang Lei
Division of Interventional Radiology of Guangdong General Hospital, Guangdong Academy of Medical Science, Guangzhou 510080, China.
Zhonghua Yi Xue Za Zhi. 2010 Aug 17;90(31):2187-92.
To provide more evidence sources to the standard treatment for patients with advanced hepatocellular carcinoma, the writer analyze patients' time to progression (TTP) and overall survival (OS) after patients receiving transcatheter arterial chemoembolization (TACE) combined with sorafenib as a treatment of advanced hepatocellular carcinoma (HCC); observe the healing effect embolization combined with anti-angiogenic treatment for advanced hepatocellular carcinoma; and also analyze treatment of security.
There are 36 patients, 33 male and 3 female had been Pathologically or clinical diagnosis. After receiving Transcatheter Arterial Chemoembolization (TACE) therapy, in the following 3 to 7 days, this group of patients continuously take sorafenib (brand name: Nexavar) (per tablet 200 mg), 2 tablets each time, 2 times a day. Every 4 to 8 weeks is called as one period of treatment. Referring to RECIST Evaluation, the writers mainly observe patients' tumor progression (TTP) and overall survival (OS), record adverse events. Using life table method to analyze survival rate, using Kaplan-Meier method to analyze all the survival curves.
Till March, 2010, 14 of 36 evaluable patients died and 22 survive; the median time to tumor progression (mTTP) to 8.62 months (95%CI: 6.51-10.24 months); the median survival time (mOS) of 12.41 months (95%CI: 9.57-14.80 months). The overall survival rate to observation period is 61.1%; 36 patients had been studied, 22 survive. Among the survivals, there is no CR cases, and 1 case PR, 15 patients SD, 6 patients PD; disease control rate (DCR) (CR + PR + SD) is 44.4%. The side effects of taking Sorafenib mainly are hand-foot skin reaction, diarrhea, fatigue and loss of appetite. These side effects can be markedly eased after symptomatic treatment.
Combined with sorafenib treatment may give patients with advanced hepatocellular carcinoma a longer longevity and keep the disease in a steady state. This therapy can be added into the treatments to patients with advanced hepatocellular carcinoma. The side effects of taking Sorafenib (Nexavar) could be stand.
为晚期肝细胞癌患者的标准治疗提供更多证据来源,作者分析了经动脉化疗栓塞术(TACE)联合索拉非尼治疗晚期肝细胞癌(HCC)患者后的疾病进展时间(TTP)和总生存期(OS);观察栓塞联合抗血管生成治疗晚期肝细胞癌的疗效;并分析治疗的安全性。
36例患者,男33例,女3例,经病理或临床诊断。接受经动脉化疗栓塞术(TACE)治疗后,在接下来的3至7天内,该组患者持续服用索拉非尼(商品名:多吉美)(每片200mg),每次2片,每日2次。每4至8周为一个治疗周期。参照RECIST评估标准,主要观察患者的肿瘤进展(TTP)和总生存期(OS),记录不良事件。采用寿命表法分析生存率,采用Kaplan-Meier法分析所有生存曲线。
至2010年3月,36例可评估患者中14例死亡,22例存活;肿瘤进展的中位时间(mTTP)为8.62个月(95%CI:6.51 - 10.24个月);中位生存时间(mOS)为12.41个月(95%CI:9.57 - 14.80个月)。观察期的总生存率为61.1%;36例患者纳入研究,22例存活。存活患者中,无CR病例,PR 1例,SD 15例,PD 6例;疾病控制率(DCR)(CR + PR + SD)为44.4%。服用索拉非尼的副作用主要为手足皮肤反应、腹泻、乏力和食欲减退。对症治疗后这些副作用可明显缓解。
联合索拉非尼治疗可能使晚期肝细胞癌患者寿命延长,病情保持稳定。该治疗方法可纳入晚期肝细胞癌患者的治疗方案中。服用索拉非尼(多吉美)的副作用可以耐受。