Efficacy and safety of hepatic arterial infusion chemotherapy combined with tyrosine kinase inhibitors and immune checkpoint inhibitors in the treatment of advanced hepatocellular carcinoma with portal vein tumor thrombosis in the main trunk

Qi Liu, Ying Zhang, Jingwen Zhang, Luhao Chen, Yi Yang, Yan Liu
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Abstract

To evaluate the efficacy and safety of mFOLFOX-based hepatic arterial infusion chemotherapy (HAIC) combined with tyrosine kinase inhibitors (TKIs) and immune checkpoint inhibitors (ICIs) in the treatment of advanced hepatocellular carcinoma (HCC) with portal vein tumor thrombosis (PVTT)This retrospective study included patients who received mFOLFOX-based HAIC combined with TKIs and ICIs from January 2021 to January 2023. The primary outcome was the objective response rate of PVTT response, and the secondary outcomes were 6-month, 1-year survival rate, overall survival (OS), and corresponding adverse events and complications were also evaluated. PVTT responses were assessed using ITK-SNAP software.A total of 37 patients were included in the analysis, 18.92% achieved a complete response and 56.76% achieved a partial response in PVTT response. The objective response rate (ORR) of PVTT was 75.68%. The 6-month survival rate was 89%, the 1-year survival rate was 66%, and the median OS was 15.8 months. In univariate analysis, Child-Pugh score (P=0.010) was important factor for predicting OS; in multivariate analysis, Child-Pugh score (P=0.015, HR= 3.089, 95%CI: 1.250–7.633) was the important factor for predicting OS. In terms of adverse reactions, the most common adverse reactions associated with HAIC are pain and thrombocytopenia associated with oxaliplatin.FOLFOX-based HAIC combined with TKIs and ICIs induced an objective response rate of 75.68% in PVTT.FOLFOX-based HAIC combined with TKIs and ICIs provides more treatment options for PVTT.
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肝动脉灌注化疗联合酪氨酸激酶抑制剂和免疫检查点抑制剂治疗伴有主干门静脉肿瘤血栓的晚期肝细胞癌的有效性和安全性
这项回顾性研究纳入了2021年1月至2023年1月期间接受基于mFOLFOX的肝动脉输注化疗(HAIC)联合酪氨酸激酶抑制剂(TKIs)和免疫检查点抑制剂(ICIs)治疗伴门静脉肿瘤血栓形成(PVTT)的晚期肝细胞癌(HCC)患者。主要结果为PVTT反应的客观反应率,次要结果为6个月、1年生存率、总生存率(OS),同时还评估了相应的不良事件和并发症。PVTT反应采用ITK-SNAP软件进行评估。共有37例患者纳入分析,18.92%的患者获得完全反应,56.76%的患者获得部分反应。PVTT的客观反应率(ORR)为75.68%。6个月生存率为89%,1年生存率为66%,中位生存期为15.8个月。在单变量分析中,Child-Pugh评分(P=0.010)是预测OS的重要因素;在多变量分析中,Child-Pugh评分(P=0.015,HR=3.089,95%CI:1.250-7.633)是预测OS的重要因素。在不良反应方面,HAIC最常见的不良反应是与奥沙利铂相关的疼痛和血小板减少。基于FOLFOX的HAIC联合TKIs和ICIs治疗PVTT的客观反应率为75.68%。
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