首页> 外文期刊>Frontiers in Molecular Biosciences >Efficacy and Safety of TACE Combined With Sorafenib Plus Immune Checkpoint Inhibitors for the Treatment of Intermediate and Advanced TACE-Refractory Hepatocellular Carcinoma: A Retrospective Study
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Efficacy and Safety of TACE Combined With Sorafenib Plus Immune Checkpoint Inhibitors for the Treatment of Intermediate and Advanced TACE-Refractory Hepatocellular Carcinoma: A Retrospective Study

机译:TACE与Sorafenib加上免疫检查点抑制剂的疗效和安全性用于治疗中间和晚期TACE - 难治性肝细胞癌:回顾性研究

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Purpose The study aims to retrospectively investigate the efficacy and safety of sorafenib combined with transarterial chemoembolization (TACE) (TACE Sor) vs. TACE combined with sorafenib plus immune checkpoint inhibitors (TACE Sor ICIs) in treating intermediate and advanced TACE-refractory hepatocellular carcinoma (HCC). Materials and Methods This study was approved by the ethics committee of Lisui Hospital, Zhejiang University, China. From January 2016 to June 2020, 51 eligible patients with intermediate or advanced TACE-refractory HCC received TACE Sor (n=29) or TACE Sor ICIs (n=22). The differences in tumor response, adverse events (AEs), progression-free survival (PFS), and overall survival (OS) were compared between the two groups. Factors affecting PFS and OS were determined by Cox regression. Results The disease control rate was higher in the TACE Sor ICIs group than in the TACE Sor group (81.82% vs 55.17%, P=0.046). Compared with the TACE Sor group, PFS and OS were prolonged in the TACE Sor ICIs group (median PFS: 16.26 vs 7.30 months, P0.001; median OS: 23.3 vs 13.8 months, P=0.012). Multivariate analysis showed that BCLC stage, alpha-fetoprotein and treatment were independent factors of PFS; BCLC, Child-Pugh class, ablation after disease progression and treatment were independent predictive factors of OS. Four patients in the TACE Sor ICIs group and three patients in the TACE Sor group suffered from dose reduction or interruption (18.18% vs 10.34%, P=0.421). The incidence of ICI-related AEs in the TACE Sor ICIs group was well controlled.Conclusion The therapeutic schedule of TACE Sor ICIs demonstrated efficacy and safety in intermediate and advanced TACE-refractory HCC.
机译:目的该研究旨在回顾性研究索拉非尼与横冲化疗(TACE)(TACE SOR)与Sorafenib Plus免疫检查点抑制剂(TACE SOR ICIS)联合治疗中间体和先进的TACE-REFTORY肝细胞癌(TACE SOR ICIS)的疗效和安全性HCC)。本研究的材料和方法由浙江大学利益医院伦理委员会批准。从2016年1月至2020年6月到6月,51名符合条件的中间体或晚期TACE-REMETRY HCC患者接受TACE SOR(n = 29)或TACE SOR ICIS(n = 22)。在两组之间比较了两组之间的肿瘤反应,不良事件(AES),不良事件(AES),无进展存活(PFS)和总存活(OS)。影响PFS和OS的因素由COX回归确定。结果TACE SO INCIS组疾病控制率高于TACE SOR组(81.82%Vs 55.17%,P = 0.046)。与TACE SOR组相比,在TACE SOR ICIS组中延长了PFS和OS(中位数:16.26 VS 7.30个月,P <0.001;中位OS:23.3 VS 13.8个月,P = 0.012)。多变量分析表明,BCLC阶段,α-胎儿蛋白和治疗是PFS的独立因素; BCLC,Child-Pugh类,疾病进展后的消融是OS的独立预测因素。在TACE SOR ICIS组中有四名患者和TACE SOR组中的三名患者患有剂量降低或中断(18.18%Vs 10.34%,P = 0.421)。 TACE SOR ICIS组中ICI相关AES的发病率良好。结论TACE SOR ICIS的治疗时间表在中间体和先进的TACE-RESTORY HCC中表现出疗效和安全性。

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