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Efficacy and safety of hepatic artery infusion chemotherapy combined with tyrosine kinase inhibitors plus programmed death-1 inhibitors for hepatocellular carcinoma refractory to transarterial chemoembolization.

作者信息

Lin Long-Wang, Ke Kun, Yan Le-Ye, Chen Rong, Huang Jing-Yao

机构信息

Department of Interventional Radiology, Fujian Medical University Union Hospital, Fuzhou, China.

出版信息

Front Oncol. 2023 May 3;13:1178428. doi: 10.3389/fonc.2023.1178428. eCollection 2023.


DOI:10.3389/fonc.2023.1178428
PMID:37207144
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10189040/
Abstract

BACKGROUND: The subsequent therapy for hepatocellular carcinoma (HCC) patients with refractory to transarterial chemoembolization (TACE) is still controversial. This study was performed to evaluate the efficacy and safety of combination therapy comprising hepatic artery infusion chemotherapy (HAIC), lenvatinib, and programmed death-1 inhibitors relative to HAIC combined with lenvatinib. METHODS: In this single-center retrospective study, we analyzed data from HCC patients with refractory to TACE from June 2017 to July 2022. Primary study outcomes were overall survival (OS) and progression-free survival (PFS), while the secondary outcomes were the objective response rate (ORR), disease control rate (DCR), and treatment-related adverse events. RESULTS: We enrolled 149 patients finally, including 75 patients who received HAIC combined with lenvatinib plus PD-1 inhibitors therapy (HAIC+L+P group) and 74 patients who received HAIC combined with lenvatinib therapy (HAIC+L group). The median OS in the HAIC+L+P group (16.0; 95% CI: 13.618.3 months) was significantly higher compared to the HAIC+L group (9.0; 95% CI: 6.511.4 months) ( = 0.002), while the median PFS in the HAIC+L+P group (11.0; 95% CI: 8.613.3 months) was significantly higher compared to the HAIC+L group (6.0; 95% CI: 5.06.9 months) ( < 0.001). Significant between-group differences in DCR ( = 0.027) were found. Additionally, 48 pairs of patients were matched after propensity matching analysis. The survival prognosis between two groups before propensity matching is similar to that after propensity matching. Moreover, the percentage of patients with hypertension in the HAIC+L+P group was significantly higher compared to the HAIC+L group (28.00% vs. 13.51%; = 0.029). CONCLUSIONS: A combination therapy of HAIC, lenvatinib, and programmed death-1 inhibitors significantly improved oncologic response and prolonged survival duration, showing a better survival prognosis for HCC patients with refractory toTACE.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8d/10189040/04d21a2212f6/fonc-13-1178428-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8d/10189040/9838f27e5a2c/fonc-13-1178428-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8d/10189040/4df25cbf83cd/fonc-13-1178428-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8d/10189040/e936ec8031f9/fonc-13-1178428-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8d/10189040/e88ad174023d/fonc-13-1178428-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8d/10189040/04d21a2212f6/fonc-13-1178428-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8d/10189040/9838f27e5a2c/fonc-13-1178428-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8d/10189040/4df25cbf83cd/fonc-13-1178428-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8d/10189040/e936ec8031f9/fonc-13-1178428-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8d/10189040/e88ad174023d/fonc-13-1178428-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8d/10189040/04d21a2212f6/fonc-13-1178428-g005.jpg

相似文献

[1]
Efficacy and safety of hepatic artery infusion chemotherapy combined with tyrosine kinase inhibitors plus programmed death-1 inhibitors for hepatocellular carcinoma refractory to transarterial chemoembolization.

Front Oncol. 2023-5-3

[2]
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[3]
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[4]
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[8]
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[9]
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引用本文的文献

[1]
Efficacy of combined TAE, HAIC, targeted, and immunotherapy in unresectable HCC: a multicenter propensity score matching study.

Sci Rep. 2025-7-1

[2]
Hepatic artery infusion chemotherapy plus an immune checkpoint inhibitor and lenvatinib for the treatment of biliary tract carcinoma.

World J Surg Oncol. 2025-6-13

[3]
Efficacy and safety of hepatic artery infusion chemotherapy conjunction with tyrosine kinase inhibitors and programmed death-1 inhibitors for unresectable/advanced hepatocellular carcinoma: a meta-analysis.

Eur J Gastroenterol Hepatol. 2025-9-1

[4]
Adverse events associated with hepatic arterial infusion chemotherapy and its combination therapies in hepatocellular carcinoma: a systematic review.

Front Immunol. 2025-3-3

[5]
Enhanced antitumor activity of combined hepatic arterial infusion chemotherapy with Lenvatinib and PD-1 inhibitors in unresectable hepatocellular carcinoma: a meta-analysis.

Front Oncol. 2025-2-12

[6]
Hepatic arterial infusion chemotherapy combined with lenvatinib and PD-1 inhibitors versus lenvatinib and PD-1 inhibitors for unresectable HCC: a meta-analysis.

Front Oncol. 2024-12-24

[7]
Roles of clinical application of lenvatinib and its resistance mechanism in advanced hepatocellular carcinoma (Review).

Am J Cancer Res. 2024-9-15

[8]
Hepatic arterial infusion chemotherapy for hepatocellular carcinoma refractory to transarterial chemoembolization: exploring the influence of prior transarterial chemoembolization and additional transarterial chemoembolization on survival outcomes.

J Gastrointest Oncol. 2024-4-30

[9]
Efficacy and safety of hepatic arterial infusion chemotherapy combined with lenvatinib and PD-1 inhibitors for advanced hepatocellular carcinoma with macrovascular invasion.

World J Surg Oncol. 2024-5-6

[10]
Efficacy of Lenvatinib Combined with Transcatheter Intra-Arterial Therapies for Patients with Advanced-Stage of Hepatocellular Carcinoma: A Propensity Score Matching.

Int J Mol Sci. 2023-9-5

本文引用的文献

[1]
Outcomes and prognostic factors in initially unresectable hepatocellular carcinoma treated using conversion therapy with lenvatinib and TACE plus PD-1 inhibitors.

Front Oncol. 2023-1-30

[2]
Transarterial Chemoembolization Followed by Hepatic Arterial Infusion Chemotherapy Combined a Tyrosine Kinase Inhibitor for Treatment of Large Hepatocellular Carcinoma.

Curr Cancer Drug Targets. 2023

[3]
Hepatic arterial infusion chemotherapy for advanced hepatocellular carcinoma in the era of chemo-diversity.

Clin Mol Hepatol. 2023-7

[4]
Role of Transarterial Chemoembolization in the Treatment of Hepatocellular Carcinoma.

J Clin Transl Hepatol. 2023-4-28

[5]
History of Transcatheter Arterial Chemoembolization Predicts the Efficacy of Hepatic Arterial Infusion Chemotherapy in Hepatocellular Carcinoma Patients.

Acta Med Okayama. 2022-12

[6]
Hepatic Arterial Infusion of Oxaliplatin, Fluorouracil, and Leucovorin Versus Sorafenib for Hepatocellular Carcinoma Refractory to Transarterial Chemoembolization: Retrospective Subgroup Analysis of 2 Prospective Trials.

Technol Cancer Res Treat. 2022

[7]
Hepatic Arterial Infusion Chemotherapy with Oxaliplatin Plus Raltitrexed as an Alternative Option in Advanced Hepatocellular Carcinoma Patients with Failure of, or Unsuitability for, Transarterial Chemoembolization.

Medicina (Kaunas). 2022-9-24

[8]
Efficacy and safety of hepatic arterial infusion chemotherapy combined with programmed cell death protein-1 antibody and lenvatinib for advanced hepatocellular carcinoma.

Front Med (Lausanne). 2022-9-1

[9]
Subsequent Treatment after Transarterial Chemoembolization Failure/Refractoriness: A Review Based on Published Evidence.

J Clin Transl Hepatol. 2022-8-28

[10]
Lenvatinib, toripalimab plus hepatic arterial infusion chemotherapy in patients with high-risk advanced hepatocellular carcinoma: A biomolecular exploratory, phase II trial.

Eur J Cancer. 2022-10

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