Department of Interventional Oncology, Fujian Cancer Hospital & Fujian Medical University Cancer Hospital, Fuzhou, No. 420 Fuma Road, Fuzhou, 350014, China.
BMC Cancer. 2018 Nov 19;18(1):1131. doi: 10.1186/s12885-018-5081-3.
Hepatocellular carcinoma (HCC) is a common cancer worldwide, with a poor prognosis. Most patients are diagnosed at advanced stages and are only eligible for palliative therapy. Therefore, this study aimed to evaluate the safety and efficacy of transcatheter arterial chemoembolization (TACE) combined with apatinib (TACE-apatinib) treatment and TACE-alone treatment for Barcelona Clinic Liver Cancer stage C HCC.
We retrospectively reviewed 80 consecutive patients with BCLC stage C HCC who received TACE-apatinib or TACE-alone as the initial treatment. We compared the clinical and laboratory outcomes, imaging findings at 1 and 3 months after TACE, tumor response, time to progression (TTP), overall survival (OS), and adverse events between both groups.
The overall response rate was higher in the TACE-apatinib group than in the TACE-alone group at 1 and 3 months after treatment (66.7% vs 39.6%, respectively, P = 0.020; 45.8% vs 17.6%, respectively, P = 0.021). The median TTP and OS in the TACE-apatinib group were longer than those of the TACE-alone group (TTP: 6.3 months vs 3.5 months, respectively, P = 0.002; OS: 13.0 months vs 9.9 months, respectively, P = 0.041). Apatinib-associated side effects such as hypertension, hand-foot syndrome, oral ulcers, proteinuria, and diarrhea were more prevalent in the TACE-apatinib group than in TACE-alone group (P < 0.05).
Compared to TACE-alone treatment, TACE-apatinib increased the TTP, OS, and tumor-response rate at 1 and 3 months after treatment of BCLC stage C HCC without any significant increase in severe adverse events.
肝细胞癌(HCC)是一种常见的全球癌症,预后较差。大多数患者在晚期被诊断出来,仅适合姑息治疗。因此,本研究旨在评估经导管动脉化疗栓塞(TACE)联合阿帕替尼(TACE-阿帕替尼)治疗与 TACE 单独治疗巴塞罗那临床肝癌(BCLC)C 期 HCC 的安全性和疗效。
我们回顾性分析了 80 例接受 TACE-阿帕替尼或 TACE 单独治疗作为初始治疗的 BCLC C 期 HCC 患者。我们比较了两组患者的临床和实验室结局、TACE 后 1 个月和 3 个月的影像学发现、肿瘤反应、无进展生存期(TTP)、总生存期(OS)和不良事件。
TACE-阿帕替尼组治疗后 1 个月和 3 个月的总体缓解率高于 TACE 单独组(分别为 66.7%比 39.6%,P=0.020;45.8%比 17.6%,P=0.021)。TACE-阿帕替尼组的中位 TTP 和 OS 长于 TACE 单独组(TTP:6.3 个月比 3.5 个月,P=0.002;OS:13.0 个月比 9.9 个月,P=0.041)。TACE-阿帕替尼组比 TACE 单独组更常见与阿帕替尼相关的不良反应,如高血压、手足综合征、口腔溃疡、蛋白尿和腹泻(P<0.05)。
与 TACE 单独治疗相比,TACE-阿帕替尼在不增加严重不良事件的情况下,增加了 BCLC C 期 HCC 患者 TACE 后 1 个月和 3 个月的 TTP、OS 和肿瘤反应率。