HAIC plus lenvatinib and tislelizumab for advanced hepatocellular carcinoma with Vp4 portal vein invasion

被引:0
|
作者
Tang, Shuangyan [1 ,2 ]
Shi, Feng [3 ]
Xiao, Yi [4 ]
Cai, Hongjie [1 ]
Ma, Ping [5 ]
Zhou, Yuanmin [5 ]
Wu, Zhiqiang [1 ]
Chen, Song [6 ]
Guo, Wenbo [1 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Intervent Radiol, Guangzhou 510062, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 8, Dept Radiol, Shenzhen 518033, Peoples R China
[3] Guangdong Prov Peoples Hosp, Dept Intervent Radiol, Guangzhou 519041, Peoples R China
[4] Sun Yat sen Univ, Affiliated Hosp 1, Ctr Hepatopancreatobiliary Surg, Guangzhou, Peoples R China
[5] Twelfth Peoples Hosp Guangzhou, Dept Oncol, Guangzhou 510620, Peoples R China
[6] Sun Yat Sen Univ, Guangdong Prov Clin Res Ctr Canc, Dept Minimally Invas Intervent Therapy, State Key Lab Oncol South China,Canc Ctr, Guangzhou 510060, Peoples R China
基金
中国国家自然科学基金;
关键词
Combination therapy; Cox regression analyses; Hepatic artery infusion chemotherapy; Kaplan-Meier method; Overall survival; PD-1; inhibitor; Progression-free survival; Propensity score matching; Safety; Portal vein thrombus regression; ARTERIAL INFUSION CHEMOTHERAPY; THROMBOSIS; RISK;
D O I
10.1007/s12072-024-10762-7
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/objective The treatment strategy for hepatocellular carcinoma (HCC) with Vp4 (main trunk) portal vein tumor thrombosis (PVTT) remains controversial due to the dismal prognosis. We aimed to investigate the efficacy and safety of hepatic arterial infusion chemotherapy (HAIC) plus lenvatinib and tislelizumab in these patients. Methods This multicenter retrospective study included treatment-naive HCC patients with Vp4 PVTT from 2017 to 2022. They were treated with HAIC plus lenvatinib and tislelizumab (HLP group) or HAIC alone (HAIC group). Overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and adverse events (AEs) were assessed. Propensity score matching (PSM) was performed to reduce bias. Results In this study, 155 HCC patients with Vp4 PVTT were included, with 38 in the HLP group and 117 in the HAIC group, with 35 per group matched by PSM. The HLP group showed longer median OS (23.2 vs. 6.9 months; HR 0.333, p < 0.001) and PFS (6.6 vs. 2.4 months; HR 0.403, p = 0.002) than the HAIC group. Higher ORR for tumor (77.1% vs. 42.9%, p = 0.003) and PVTT (51.4% vs. 22.9%, p = 0.025) was observed in the HLP group. More patients underwent hepatectomy post-conversion therapy (15.8% vs. 0.9%). Grade 3/4 AEs were higher in the HLP group (47.4% vs. 35.0%), but there was no significant difference, and no grade 5 AEs occurred in either group. Conclusions HAIC combined with lenvatinib and tislelizumab may be a promising treatment in patients with HCC and Vp4 PVTT because of the improved prognosis and acceptable safety profile.
引用
收藏
页码:106 / 117
页数:12
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