Liao Yadi, Zheng Yun, He Wei, Li Qijiong, Shen Jingxian, Hong Jian, Zou Ruhai, Qiu Jiliang, Li Binkui, Yuan Yunfei
State Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong 510060, P.R. China; Department of Hepatobiliary Oncology, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong 510060, P.R. China.
Department of Medical Imaging and Interventional Center, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong 510060, P.R. China.
Oncol Lett. 2017 Feb;13(2):984-992. doi: 10.3892/ol.2016.5525. Epub 2016 Dec 20.
Sorafenib is the standard systemic treatment for patients with advanced hepatocellular carcinoma (HCC); however, its therapeutic value in patients with HCC following resection remains controversial. The current retrospective study was undertaken to assess the effects of sorafenib treatment following surgical resection in patients with advanced HCC disease who were at a high risk for recurrence. Between July 2010 and July 2013, a consecutive cohort of 42 patients with advanced HCC and at a high risk of recurrence (i.e., those with portal vein tumor thrombosis, adjacent organ involvement or tumor rupture) who underwent resection were analyzed. The patients were categorized into the sorafenib group (n=14) or the best supportive care (BSC) group (n=28). Although the histological grade, Barcelona Clinic Liver Cancer Stage, tumor size, nodule number and proportion of patients with high serum α-fetoprotein levels were comparable between the sorafenib and BSC groups, those receiving sorafenib following resection had significantly longer disease-free survival (DFS) of 5.2 months [95% confidence interval (CI), 1.2-9.2 months] compared with the BSC group [1.8 months (95% CI, 0.6-3.0 months)]. No differences in overall survival were noted between the groups. Furthermore, no drug-related adverse events resulted in discontinuation of sorafenib therapy. Univariate log-rank analysis revealed that sorafenib treatment (P=0.002) and treatment prior to resection (P=0.012) were significantly associated with longer DFS; however, sorafenib therapy (P=0.027) and tumor size (P=0.028) were associated with longer DFS by multivariate analysis. Furthermore, sorafenib was well-tolerated and improved DFS in patients with advanced HCC who underwent hepatic resection. Thus, tumor resection followed by sorafenib therapy may represent an effective therapeutic strategy for patients with advanced HCC. This possibility should be confirmed in larger, multicenter studies.
索拉非尼是晚期肝细胞癌(HCC)患者的标准全身治疗药物;然而,其在肝癌切除术后患者中的治疗价值仍存在争议。本项回顾性研究旨在评估索拉非尼治疗对复发风险高的晚期HCC疾病手术切除患者的影响。2010年7月至2013年7月,对连续42例接受手术切除的晚期HCC且复发风险高(即伴有门静脉肿瘤血栓形成、邻近器官受累或肿瘤破裂)的患者进行了分析。患者被分为索拉非尼组(n = 14)或最佳支持治疗(BSC)组(n = 28)。尽管索拉非尼组和BSC组之间的组织学分级、巴塞罗那临床肝癌分期、肿瘤大小、结节数量以及血清甲胎蛋白水平高的患者比例相当,但与BSC组相比,切除术后接受索拉非尼治疗的患者无病生存期(DFS)显著延长,为5.2个月[95%置信区间(CI),1.2 - 9.2个月],而BSC组为1.8个月(95%CI,0.6 - 3.0个月)。两组之间总生存期无差异。此外,没有药物相关不良事件导致索拉非尼治疗中断。单因素对数秩分析显示,索拉非尼治疗(P = 0.002)和切除术前治疗(P = 0.012)与更长的DFS显著相关;然而,多因素分析显示索拉非尼治疗(P = 0.027)和肿瘤大小(P = 0.028)与更长的DFS相关。此外,索拉非尼耐受性良好,可改善接受肝切除的晚期HCC患者的DFS。因此,肿瘤切除后进行索拉非尼治疗可能是晚期HCC患者的一种有效治疗策略。这种可能性应在更大规模的多中心研究中得到证实。