Department of Gastroenterology, China Medical University Hospital, China Medical University, Taichung, 40000 Taiwan, China.
World J Gastroenterol. 2012 Feb 7;18(5):466-71. doi: 10.3748/wjg.v18.i5.466.
To evaluate the efficacy of thalidomide in combination with other therapies to treat patients with advanced hepatocellular carcinoma (HCC).
We performed a retrospective analysis of all patients with HCC who were treated with thalidomide for at least two months. The medical records of patients with HCC who were treated at our institution between April 2003 and March 2008 were reviewed. Image studies performed before and after treatment, tumor response, overall survival, and the decrease in α-fetoprotein (AFP) levels were evaluated.
A total of 53 patients with HCC received either 100 or 200 mg/d of thalidomide. The patient population consisted of 9 women and 44 men with a median age of 61 years. Thirty patients (56.6%) were classified as Child-Pugh A, and 12 patients (22.6%) were classified as Child-Pugh B. Twenty-six patients had portal vein thrombosis (49.1%), and 25 patients had extrahepatic metastasis (47.1%). The median duration of thalidomide treatment was 6.0 mo. Six of the 53 patients achieved a confirmed response (11.3%), one achieved a complete response (1.9%) and 5 achieved a partial response (9.4%). The disease control rate (CR + PR + SD) was 28.3% (95% CI: 17.8-42.4), and the median overall survival rate was 10.5 mo. The 1- and 2-year survival rates were 45% and 20%, respectively. Only one complete response patient showed an improved overall survival rate of 66.8 mo. Sixteen patients (30.2%) showed more than a 50% decrease in their serum AFP levels from baseline, indicating a better response rate (31.3%), disease control rate (43.8%), and overall survival time (20.7 mo). The therapy was well tolerated, and no significant toxicities were observed.
Thalidomide was found to be safe for advanced HCC patients, demonstrating anti-tumor activity including response, survival, and AFP decreases of greater than 50% from baseline.
评估沙利度胺联合其他疗法治疗晚期肝细胞癌(HCC)患者的疗效。
我们对至少接受 2 个月沙利度胺治疗的所有 HCC 患者进行了回顾性分析。回顾了 2003 年 4 月至 2008 年 3 月期间在我院接受治疗的 HCC 患者的病历。评估了治疗前后的影像学研究、肿瘤反应、总生存期和甲胎蛋白(AFP)水平的降低情况。
共有 53 例 HCC 患者接受了 100 或 200 mg/d 的沙利度胺治疗。患者人群包括 9 名女性和 44 名男性,中位年龄为 61 岁。30 例(56.6%)患者为 Child-Pugh A 级,12 例(22.6%)患者为 Child-Pugh B 级。26 例患者有门静脉血栓形成(49.1%),25 例患者有肝外转移(47.1%)。沙利度胺治疗的中位持续时间为 6.0 个月。53 例患者中,有 6 例(11.3%)确认缓解,1 例(1.9%)完全缓解,5 例(9.4%)部分缓解。疾病控制率(CR + PR + SD)为 28.3%(95%CI:17.8-42.4),中位总生存期为 10.5 个月。1 年和 2 年生存率分别为 45%和 20%。仅 1 例完全缓解患者的总生存率改善至 66.8 个月。16 例(30.2%)患者的血清 AFP 水平较基线下降超过 50%,表明缓解率(31.3%)、疾病控制率(43.8%)和总生存期(20.7 个月)更好。该疗法耐受良好,未观察到明显的毒性。
沙利度胺对晚期 HCC 患者是安全的,具有抗肿瘤活性,包括反应、生存和 AFP 从基线下降超过 50%。