Comparative analysis of efficacy and safety between D-TACE plus HAIC plus lenvatinib and D-TACE plus lenvatinib in the treatment of unresectable massive hepatocellular carcinoma

被引:0
|
作者
Lu, Haohao [1 ,2 ]
Liang, Bin [1 ,2 ]
Zheng, Chuansheng [1 ,2 ]
Xia, Xiangwen [1 ,2 ]
机构
[1] Huazhong Univ Sci & Technol, Union Hosp, Tongji Med Coll, Dept Radiol, Jiefang Ave 1277, Wuhan 430022, Peoples R China
[2] Hubei Prov Key Lab Mol Imaging, Wuhan 430022, Peoples R China
关键词
Massive hepatocellular carcinoma; Drug-eluting bead transarterial chemoembolization; Hepatic arterial infusion chemotherapy; Targeted therapy; Tyrosine kinase inhibitor; Lenvatinib; Interventional treatment; HEPATIC ARTERIAL INFUSION; TRANSARTERIAL CHEMOEMBOLIZATION; EMBOLIZATION; CHEMOTHERAPY; OXALIPLATIN; DOXORUBICIN; SURVIVAL; LIPIODOL; FOLFOX; LARGER;
D O I
10.1186/s12885-024-13179-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
ObjectiveThe aim of this study was to investigate the efficacy and safety of the combined treatment regimen of D-TACE, HAIC, and Lenvatinib in patients with massive hepatocellular carcinoma, with the goal of providing a safer and more effective therapeutic strategy for individuals suffering from massive hepatocellular carcinoma. Materials and methodsA retrospective analysis was conducted using clinical data from 118 patients with unresectable massive hepatocellular carcinoma who underwent treatment at the Interventional Department of Wuhan Union Hospital between June 2018 and December 2021. Based on the treatment approach, the patients were divided into two groups: the D-TACE + HAIC + Lenvatinib group (N = 54) and the D-TACE + Lenvatinib group (N = 64). The primary study endpoints included the objective response rate (ORR), disease control rate (DCR), overall survival (OS), and progression-free survival (PFS) of the two groups. Additionally, the occurrence of treatment-related adverse events in both groups was considered as a secondary study endpoint. ResultsFollowing the treatment, the D-TACE + HAIC + Lenvatinib group exhibited significantly higher ORR and DCR compared to the D-TACE + Lenvatinib group (68.5% vs. 43.8%, 90.7% vs. 73.4%, P < 0.05). Moreover, the D-TACE + HAIC + Lenvatinib group demonstrated longer mPFS and mOS in comparison to the D-TACE + Lenvatinib group (8.6 months vs. 6.6 months, P = 0.005; 19.5 months vs. 14.1 months, P < 0.001). There was no statistically significant difference in the occurrence rate of common treatment-related adverse events between the TACE + HAIC + Lenvatinib group and the D-TACE + Lenvatinib group (P > 0.05). ConclusionThe combined treatment regimen of D-TACE, HAIC, and Lenvatinib demonstrated superior therapeutic efficacy and safety in managing unresectable massive hepatocellular carcinoma. This combination therapy may serve as a viable option for improving the prognosis of patients with unresectable massive hepatocellular carcinoma.
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页数:14
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