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.
引用
收藏
页数:14
相关论文
共 50 条
  • [41] Efficacy and safety analysis of TACE + Donafenib + Toripalimab versus TACE + Sorafenib in the treatment of unresectable hepatocellular carcinoma: a retrospective study
    Haohao Lu
    Bin Liang
    Xiangwen Xia
    Chuansheng Zheng
    BMC Cancer, 23
  • [42] Efficacy and Safety of Transarterial Chemoembolization Plus Lenvatinib with or Without Tislelizumab as the First-Line Treatment for Unresectable Hepatocellular Carcinoma: A Propensity Score Matching Analysis
    Jiang, Jiayun
    Zhang, Hui
    Lai, Jiejuan
    Zhang, Shiyu
    Ou, Yanjiao
    Fu, Yu
    Zhang, Leida
    JOURNAL OF HEPATOCELLULAR CARCINOMA, 2024, 11 : 1607 - 1622
  • [43] Rechallenge With Lenvatinib After Atezolizumab Plus Bevacizumab Treatment for Hepatocellular Carcinoma
    Komatsu, Shohei
    Yano, Yoshihiko
    Kido, Masahiro
    Kuramitsu, Kaori
    Gon, Hidetoshi
    Fukushima, Kenji
    Urade, Takeshi
    So, Shinichi
    Yamamoto, Atsushi
    Goto, Tadahiro
    Yanagimoto, Hiroaki
    Toyama, Hirochika
    Ueda, Yoshihide
    Kodama, Yuzo
    Fukumoto, Takumi
    ANTICANCER RESEARCH, 2022, 42 (11) : 5479 - 5486
  • [44] Correlation and efficacy of TACE combined with lenvatinib plus PD-1 inhibitor in the treatment of hepatocellular carcinoma with portal vein tumor thrombus based on immunological features
    Zou, Xinhua
    Xu, Qingyu
    You, Ran
    Yin, Guowen
    CANCER MEDICINE, 2023, 12 (10): : 11315 - 11333
  • [45] Lenvatinib plus pembrolizumab: the next frontier for the treatment of hepatocellular carcinoma?
    Rizzo, Alessandro
    Dadduzio, Vincenzo
    Ricci, Angela Dalia
    Massari, Francesco
    Di Federico, Alessandro
    Gadaleta-Caldarola, Gennaro
    Brandi, Giovanni
    EXPERT OPINION ON INVESTIGATIONAL DRUGS, 2022, 31 (04) : 371 - 378
  • [46] Safety and efficacy of DEB-TACE in combination with lenvatinib and camrelizumab for the treatment of unresectable hepatocellular carcinoma (uHCC): a two-centre retrospective study
    Zhang, Xuexian
    Wang, Ruidong
    Ding, Yuhan
    Li, Qingwei
    Feng, Xiong
    Hong, Ren
    Jun, Zhang
    Wei, Li
    FRONTIERS IN IMMUNOLOGY, 2024, 15
  • [47] Evaluating the Benefits of TACE Combined with Lenvatinib Plus PD-1 Inhibitor for Hepatocellular Carcinoma with Portal Vein Tumor Thrombus
    Zou, Xinhua
    Xu, Qingyu
    You, Ran
    Yin, Guowen
    ADVANCES IN THERAPY, 2023, 40 (04) : 1686 - 1704
  • [48] Evaluating the Benefits of TACE Combined with Lenvatinib Plus PD-1 Inhibitor for Hepatocellular Carcinoma with Portal Vein Tumor Thrombus
    Xinhua Zou
    Qingyu Xu
    Ran You
    Guowen Yin
    Advances in Therapy, 2023, 40 (4) : 1686 - 1704
  • [49] The efficacy and safety of thymosin alpha-1 combined with lenvatinib plus sintilimab in unresectable hepatocellular carcinoma: a retrospective study
    Siyang Yao
    Qiangsong Huang
    Yan Zou
    Tianqi Liu
    Yongyu Yang
    Tao Huang
    Yuanquan Zhao
    Xiaofeng Dong
    Scientific Reports, 15 (1)
  • [50] The efficacy and safety of Radiofrequency ablation combined with Lenvatinib plus Sintilimab in Unresectable Hepatocellular Carcinoma: a real-world study
    Wang, Xishu
    Sun, Ximin
    Lei, Yongrong
    Fang, Lingyan
    Wang, Yuedi
    Feng, Kai
    Xia, Feng
    BMC CANCER, 2024, 24 (01)