Ohki Takamasa, Sato Koki, Yamagami Mari, Ito Daisaku, Yamada Tomoharu, Kawanishi Koki, Kojima Kentaro, Seki Michiharu, Toda Nobuo, Tagawa Kazumi
Department of Gastroenterology, Mitsui Memorial Hospital, Kanda-Izumi-cho 1, Chiyoda-ku, Tokyo, 101-8643, Japan.
Clin Drug Investig. 2015 Nov;35(11):751-9. doi: 10.1007/s40261-015-0333-3.
Sorafenib might prevent hepatocellular carcinoma (HCC) recurrence caused by the promotion of neoangiogenesis after transarterial chemoembolization (TACE).
To evaluate the efficacy and safety of TACE followed by sorafenib for treating advanced HCC.
We retrospectively analyzed 95 advanced HCC patients treated with TACE between July 2008 and December 2012 at our institution. Twenty-four patients received TACE followed by sorafenib within 14 days (S-TACE) and 71 received TACE alone. Progression-free survival (PFS) and cumulative survival from the time of non-responsiveness to TACE were compared between groups and predictive factors for PFS were analyzed.
The median patient age was 72.2 years and 74 patients were male (77.9 %). Although median tumor size was similar between groups, the mean tumor number was significantly higher in the S-TACE versus TACE-alone group (16 vs. 8, P = 0.04). The number of prior treatments was significantly higher in the S-TACE group. Other baseline variables were similar. There were two severe adverse events in the S-TACE group and none in the TACE-alone group. Median PFS (189 vs. 106 days, P = 0.02) and median overall survival time (861 vs. 467 days, P = 0.01) from the time of non-responsiveness to TACE were significantly longer with S-TACE than TACE alone. Adjusting for significant factors in univariate analysis, multivariate analysis indicated that sorafenib administration, tumor size, and alanine transaminase were independent predictors of PFS.
TACE followed by sorafenib significantly improved PFS and survival in patients with advanced HCC unresponsive to TACE.
索拉非尼可能预防经动脉化疗栓塞术(TACE)后因促进新生血管生成导致的肝细胞癌(HCC)复发。
评估TACE联合索拉非尼治疗晚期HCC的疗效和安全性。
我们回顾性分析了2008年7月至2012年12月在我院接受TACE治疗的95例晚期HCC患者。24例患者在14天内接受TACE联合索拉非尼治疗(S-TACE组),71例仅接受TACE治疗。比较两组从对TACE无反应时起的无进展生存期(PFS)和累积生存期,并分析PFS的预测因素。
患者中位年龄为72.2岁,74例为男性(77.9%)。尽管两组间肿瘤中位大小相似,但S-TACE组的平均肿瘤数目显著高于单纯TACE组(16个对8个,P = 0.04)。S-TACE组既往治疗次数显著更多。其他基线变量相似。S-TACE组有2例严重不良事件,单纯TACE组无。从对TACE无反应时起,S-TACE组的中位PFS(189天对106天,P = 0.02)和中位总生存时间(861天对467天,P = 0.01)显著长于单纯TACE组。在单因素分析中对显著因素进行校正后,多因素分析表明索拉非尼给药、肿瘤大小和丙氨酸转氨酶是PFS的独立预测因素。
TACE联合索拉非尼显著改善了对TACE无反应的晚期HCC患者的PFS和生存期。