Shen Lujun, Chen Shuanggang, Qiu Zhiyu, Qi Han, Yuan Hui, Cao Fei, Xie Lin, Chen Qifeng, Li Wang, Fan Weijun
Department of Minimally Invasive Interventional Therapy, Sun Yat-Sen University Cancer Center; Collaborative Innovation Center of Cancer Medicine, State Key Laboratory of Oncology in South China, Sun Yat-Sen University, Guangzhou, China.
Collaborative Innovation Center of Cancer Medicine, State Key Laboratory of Oncology in South China; Zhongshan School of Medical, Sun Yat-Sen University, Guangzhou, China.
J Cancer Res Ther. 2020 Sep;16(5):1063-1068. doi: 10.4103/jcrt.JCRT_801_19.
Macroscopic vascular invasion in hepatocellular carcinoma (HCC) remains challenging to treat.
The aim of this study was to compare the efficacy of transarterial chemoembolization (TACE)-apatinib therapy with TACE treatment alone in HCC patients with macrovascular invasion, using propensity score matching (PSM).
Matched paired comparison between the TACE-apatinib and TACE alone group using 1:2 PSM was utilized.
Between 2013 and 2019, 378 patients receiving TACE-apatinib or TACE alone were included based on specific selection criteria.
Multivariate Cox regression models were used to determine the independent prognostic factors for overall survival (OS).
Of the patients included, 40 (12.5%) received TACE-apatinib treatment and 280 (87.5%) received TACE alone. Tumor sizes of patients in the TACE-apatinib group were more frequently classified as small (<5 cm) compared to those in the TACE alone group (P = 0.021; mean: 8.6 cm vs. 10.2 cm). After 1:2 PSM, 40 pairs of HCC patients with well-matched covariates were selected from the two treatment groups. Patients in the TACE-apatinib group had higher OS rates than patients in the TACE alone group (P = 0.018). The median OS times were 18.2 and 8.5 months in the TACE-apatinib and TACE alone groups, respectively. The OS hazard ratio for the choice of TACE-apatinib treatment compared to TACE treatment alone was 0.50 (95% confidence interval: 0.28-0.90; P = 0.021).
TACE combined with apatinib may result in superior OS compared to TACE therapy alone for HCC patients with macrovascular invasion.
肝细胞癌(HCC)中的宏观血管侵犯治疗仍然具有挑战性。
本研究的目的是使用倾向评分匹配(PSM)比较经动脉化疗栓塞(TACE)-阿帕替尼疗法与单纯TACE治疗对伴有大血管侵犯的HCC患者的疗效。
采用1:2 PSM对TACE-阿帕替尼组和单纯TACE组进行配对比较。
2013年至2019年期间,根据特定选择标准纳入378例接受TACE-阿帕替尼或单纯TACE治疗的患者。
使用多变量Cox回归模型确定总生存期(OS)的独立预后因素。
纳入的患者中,40例(12.5%)接受TACE-阿帕替尼治疗,280例(87.5%)接受单纯TACE治疗。与单纯TACE组相比,TACE-阿帕替尼组患者的肿瘤大小更常被分类为小肿瘤(<5 cm)(P = 0.021;平均值:8.6 cm对10.2 cm)。经过1:2 PSM后,从两个治疗组中选出40对协变量匹配良好的HCC患者。TACE-阿帕替尼组患者的OS率高于单纯TACE组患者(P = 0.018)。TACE-阿帕替尼组和单纯TACE组的中位OS时间分别为18.2个月和8.5个月。与单纯TACE治疗相比,选择TACE-阿帕替尼治疗的OS风险比为0.50(95%置信区间:0.28 - 0.90;P = 0.021)。
对于伴有大血管侵犯的HCC患者,与单纯TACE治疗相比,TACE联合阿帕替尼可能导致更好的总生存期。