Efficacy of transarterial chemoembolization-hepatic arterial infusion chemotherapy combined with targeted therapy and immunotherapy in hepatocellular carcinoma with portal vein tumor thrombosis

被引:0
作者
Hou, Xunbo [1 ]
Xu, Qiannan [2 ]
Yin, Linan [1 ]
Wang, Huiwen [1 ]
Wu, Juan [3 ]
Liu, Bowen [1 ]
He, Dongfeng [1 ]
Liu, Ruibao [1 ]
机构
[1] Harbin Med Univ, Dept Intervent Radiol, Dept Radiol, Canc Hosp, Harbin 150081, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Dept Anesthesiol, Affiliated Hosp 4, Harbin 150001, Heilongjiang, Peoples R China
[3] Third Peoples Hosp Longgang Dist, Dept Radiol, Shenzhen 518115, Peoples R China
关键词
hepatocellular carcinoma; portal vein tumor thrombosis; transarterial chemoembolization; hepatic arterial infusion chemotherapy; overall survival; progression-free survival; MANAGEMENT;
D O I
10.3892/ol.2025.15109
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma (HCC) with portal vein tumor thrombosis (PVTT) presents a notable therapeutic challenge. The efficacy of transarterial chemoembolization (TACE) combined with hepatic arterial infusion chemotherapy (HAIC) and systemic therapy using tyrosine kinase inhibitor and programmed cell death protein 1 inhibitor has not been fully explored. In the present study, the clinical data from 251 patients with HCC and PVTT treated at Harbin Medical University Cancer Hospital (Harbin, China) between January 2021 and December 2022 were retrospectively analyzed. Patients were divided into four groups: TACE-HAIC + lenvatinib + camrelizumab (Group 1; n=16), TACE + lenvatinib + camrelizumab (Group 2; n=90), HAIC + lenvatinib + camrelizumab (Group 3; n=102) and TACE alone (Group 4; n=43). Clinical data included demographics, preoperative indices, tumor characteristics, medical history, performance status, liver function, pre-treatment alpha-fetoprotein levels and adverse events. Survival outcomes [overall survival (OS) and progression-free survival (PFS)] were analyzed using Kaplan-Meier survival curves. Group 1 exhibited significantly longer OS and PFS times compared with Group 4 (both P<0.05). Adverse events, including fatigue, diarrhea, nausea, vomiting and immune-related pneumonitis, were more frequent in Group 1 (all P<0.001). Group 2 also showed improved OS and PFS times compared with Group 4 (both P<0.05), with notable differences in adverse event profiles. Group 3 demonstrated superior survival outcomes compared with Group 4 (P<0.05), although with a higher incidence of adverse events. No significant differences in OS or PFS times were observed between Groups 1 and 3, or between Groups 2 and 3, indicating comparable efficacy between TACE-HAIC + lenvatinib + camrelizumab and HAIC + lenvatinib + camrelizumab. In conclusion, TACE-HAIC combined with lenvatinib and camrelizumab significantly improved both OS and PFS times in patients with HCC and PVTT compared with TACE alone, despite a higher incidence of adverse events. This combination therapy represents a promising treatment strategy for this patient population, offering enhanced survival benefits.
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页数:9
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