Department of Oncology, The Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong, 519000, China.
Department of Gastroenterology, Cancer Hospital of Jiangxi Province, Nanchang, Jiangxi, 330029, China.
BMC Cancer. 2017 Nov 6;17(1):714. doi: 10.1186/s12885-017-3707-5.
Many studies have combined sorafenib with transcatheter arterial chemoembolization (TACE) to treat patients with advanced hepatocellular carcinoma (HCC), but the results are disputable. Thus, we conducted this meta-analysis to assess the efficacy and safety of the combination treatment in patients with advanced HCC.
Clinical data were collected from a computer search of literature published from January 2009 to June 2016 in PubMed, Web of Science, the Cochrane Library, China National Knowledge Infrastructure (CNKI), Wan Fang and the China Science and Technology Journal Database (CSTJ). The final analysis included 14 studies and 1670 patients. The primary endpoints were overall survival (OS), the objective response rate (ORR) and the disease control rate (DCR).
The combination group exhibited significantly more improvement than the group treated with TACE alone in ORR (RR =1.62, 95% confidence interval (CI) = 1.34-1.94, p < 0.00001), DCR (RR = 1.43, 95% CI = 1.26-1.62, p < 0.00001), 0.5-year OS (OR = 2.60, 95% CI = 1.57-4.29, p = 0.0002) and 1-year OS (OR = 1.88, 95% CI =1.39-2.53, p < 0.0001). The incidence of adverse events from combination therapy was increased compared to that from treatment with TACE alone, and the most commonly reported adverse events were fatigue, hand-foot skin reaction and diarrhoea, which were bearable.
The meta-analysis indicated that combination therapy is safe and efficient for clinical application.
许多研究已经将索拉非尼与经导管动脉化疗栓塞(TACE)联合用于治疗晚期肝细胞癌(HCC)患者,但结果存在争议。因此,我们进行了这项荟萃分析,以评估联合治疗对晚期 HCC 患者的疗效和安全性。
从 2009 年 1 月至 2016 年 6 月,我们通过计算机检索PubMed、Web of Science、Cochrane 图书馆、中国知网(CNKI)、万方和中国科技期刊数据库(CSTJ)中的文献,收集临床数据。最终分析纳入了 14 项研究和 1670 名患者。主要终点是总生存期(OS)、客观缓解率(ORR)和疾病控制率(DCR)。
联合组在 ORR(RR=1.62,95%置信区间[CI]为 1.34-1.94,p<0.00001)、DCR(RR=1.43,95%CI为 1.26-1.62,p<0.00001)、0.5 年 OS(OR=2.60,95%CI 为 1.57-4.29,p=0.0002)和 1 年 OS(OR=1.88,95%CI 为 1.39-2.53,p<0.0001)方面的改善明显优于单独 TACE 治疗组。与单独 TACE 治疗相比,联合治疗的不良反应发生率增加,但最常见的不良反应是疲劳、手足皮肤反应和腹泻,这些反应是可以耐受的。
这项荟萃分析表明,联合治疗在临床应用中是安全有效的。