Efficiency and safety of HAIC combined with lenvatinib and tislelizumab for advanced hepatocellular carcinoma with high tumor burden: a multicenter propensity score matching analysis.

IF 4.4 2区 医学 Q1 PHARMACOLOGY & PHARMACY Frontiers in Pharmacology Pub Date : 2025-01-07 eCollection Date: 2024-01-01 DOI:10.3389/fphar.2024.1499269
Zhonghua Zhao, Xiongying Jiang, Shiping Wen, Yanzhang Hao
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Abstract

Purpose: The present work focused on assessing whether hepatic arterial infusion chemotherapy (HAIC) combined with lenvatinib and tislelizumab was safe and effective on advanced hepatocellular carcinoma (HCC) showing high tumor burden.

Methods: In the present multicenter retrospective study, treatment-naive advanced HCC patients (BCLC stage C) showing high tumor burden (maximum diameter of intrahepatic lesion beyond 7 cm) treated with lenvatinib and tislelizumab with or without HAIC were reviewed for eligibility from June 2020 to June 2023. Baseline differences between groups were mitigated by propensity score matching (PSM). Our primary endpoint was overall survival (OS); and secondary endpoints included adverse events (AEs), progression-free survival (PFS), disease control rate (DCR) and objective response rate (ORR) according to RECIST 1.1 criteria, respectively.

Results: After eligibility reviewed, total 162 patients treated with lenvatinib and tislelizumab were enrolled: 63 patients with HAIC (HTP group), and the remaining 99 patients without HAIC (TP group). After PSM 1:1, 47 cases were evenly divided into each group. Of them, HTP group showed significant prolonged median OS compared with TP group (16.6 versus 21.0 months; hazard ratio [HR]: 0.26, 95% confidence interval [CI]: 0.35-0.98; p = 0.039), and median PFS of HTP group was also prolonged (8.9 versus 11.6 months; HR: 0.55, 95% CI: 0.34-0.87; p = 0.010). Higher DCR and ORR could be observed in HTP relative to TP groups (ORR: 53.2% versus 17.0%, p < 0.001; DCR: 87.2% versus 61.7%, p = 0.004). The severe AEs (grade 3/4) and all grades were comparable between the groups, while all of these AEs could be controlled, and AEs of grade 5 were not reported.

Conclusion: HAIC combined with lenvatinib and tislelizumab is the candidate treatment for advanced HCC patients because of its improved prognosis and acceptable safety.

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HAIC联合lenvatinib和tislelizumab治疗高肿瘤负荷晚期肝细胞癌的有效性和安全性:多中心倾向评分匹配分析
目的:评价肝动脉输注化疗(HAIC)联合lenvatinib和tislelizumab治疗高肿瘤负担的晚期肝细胞癌(HCC)是否安全有效。方法:在本多中心回顾性研究中,在2020年6月至2023年6月期间,对未接受治疗的晚期HCC患者(BCLC C期)进行了评估,这些患者显示出高肿瘤负担(肝内病变最大直径超过7cm),并接受lenvatinib和tislelizumab治疗,伴有或不伴有HAIC。通过倾向评分匹配(PSM)减轻组间基线差异。我们的主要终点是总生存期(OS);次要终点分别包括不良事件(ae)、无进展生存期(PFS)、疾病控制率(DCR)和客观缓解率(ORR)(根据RECIST 1.1标准)。结果:经过资格审查,共纳入162例lenvatinib和tislelizumab治疗的患者:63例HAIC患者(HTP组),其余99例无HAIC患者(TP组)。经1:1 PSM后,47例平均分为两组。其中,与TP组相比,HTP组的中位生存期明显延长(16.6个月比21.0个月;风险比[HR]: 0.26, 95%可信区间[CI]: 0.35-0.98;p = 0.039), HTP组的中位PFS也延长(8.9个月比11.6个月;Hr: 0.55, 95% ci: 0.34-0.87;P = 0.010)。HTP组的DCR和ORR高于TP组(ORR: 53.2% vs . 17.0%, p < 0.001;DCR: 87.2%对61.7%,p = 0.004)。严重ae(3/4级)和所有级别的ae在组间具有可比性,但这些ae均可控制,未报道5级ae。结论:HAIC联合lenvatinib和tislelizumab是晚期HCC患者的候选治疗方案,预后改善,安全性可接受。
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来源期刊
Frontiers in Pharmacology
Frontiers in Pharmacology PHARMACOLOGY & PHARMACY-
CiteScore
7.80
自引率
8.90%
发文量
5163
审稿时长
14 weeks
期刊介绍: Frontiers in Pharmacology is a leading journal in its field, publishing rigorously peer-reviewed research across disciplines, including basic and clinical pharmacology, medicinal chemistry, pharmacy and toxicology. Field Chief Editor Heike Wulff at UC Davis is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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