Efficacy and Safety of Lenvatinib Plus Programmed Death-1 Inhibitors with or Without Transarterial Chemoembolization in the Treatment of Unresectable Hepatocellular Carcinoma.

IF 4.2 3区 医学 Q2 ONCOLOGY
Journal of Hepatocellular Carcinoma Pub Date : 2024-11-25 eCollection Date: 2024-01-01 DOI:10.2147/JHC.S485047
Ming Jin, Zhi-Qing Jiang, Jia-Hui Qin, Hui-Xia Qin, Kai-Wen Jiang, Hou-Xiang Ya, Jing Gu, Mo-Rui Gui, Yao-Hua Li, Long-Kuan Xu, Hai-Xiao Fu, Xu-Hua Xiao, Shu-Qun Li
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引用次数: 0

Abstract

Purpose: Transarterial chemoembolization (TACE) is recommended as a standard therapy for intermediate-stage hepatocellular carcinoma (HCC) and is the most widely used first-line treatment for advanced HCC. This study aimed to evaluate the clinical benefits and tolerability of TACE added to a combination of lenvatinib and programmed death-1 (PD-1) inhibitor in patients with unresectable HCC (uHCC).

Patients and methods: We conducted a retrospective cohort study involving 144 patients with uHCC treated between August 2020 and August 2023. Patients received a combination of lenvatinib and a PD-1 inhibitor with or without TACE (T+L+P, n=81 or L+P, n=63, respectively). The baseline characteristics of the two groups were compared, and propensity score matching (PSM) was used to minimize bias. The study endpoints included overall survival (OS), progression-free survival (PFS), and objective response rate (ORR). Factors influencing survival rates were analyzed using Cox regression, and adverse events (AEs) were documented and assessed.

Results: Before PSM, the T+L+P group showed significantly higher ORR (64.1% vs 44.4%, p < 0.05), longer median PFS (14.3 vs 9.6 months, p < 0.05), and longer median OS (24.6 vs 19.5 months, p < 0.05) compared to the L+P group. Even post-PSM, the T+L+P group showed significantly better OS and PFS compared to the L+P group (mOS: 28.0 vs 17.6 months p=0.0011, mPFS: 15.8 vs 9.3 months, p < 0.05). Univariate and multivariate analyses identified treatment options as independent factors for PFS and OS. The safety profile of the T+L+P regimen was acceptableThe incidence and severity of adverse reactions in the T+L+P group were not significantly different compared to the L+P group (any grade, 90.1 vs 93.6%, p=0.551; grade≥3, 25.9 vs 23.8%, p=0.843).

Lenvatinib +程序性死亡-1抑制剂伴或不伴经动脉化疗栓塞治疗不可切除肝细胞癌的疗效和安全性
目的:经动脉化疗栓塞(TACE)被推荐为中期肝细胞癌(HCC)的标准治疗方法,也是晚期肝细胞癌最广泛使用的一线治疗方法。本研究旨在评估TACE联合lenvatinib和程序性死亡-1 (PD-1)抑制剂治疗不可切除HCC (uHCC)患者的临床获益和耐受性。患者和方法:我们进行了一项回顾性队列研究,纳入了144例在2020年8月至2023年8月期间接受治疗的uHCC患者。患者接受lenvatinib和PD-1抑制剂联合或不联合TACE治疗(T+L+P, n=81或L+P, n=63)。比较两组的基线特征,并使用倾向评分匹配(PSM)来最小化偏倚。研究终点包括总生存期(OS)、无进展生存期(PFS)和客观缓解率(ORR)。使用Cox回归分析影响生存率的因素,并记录和评估不良事件(ae)。结果:PSM前,T+L+P组的ORR (64.1% vs 44.4%, P < 0.05)、中位PFS (14.3 vs 9.6个月,P < 0.05)和中位OS (24.6 vs 19.5个月,P < 0.05)均显著高于L+P组。即使在psm后,T+L+P组的OS和PFS也明显优于L+P组(mOS: 28.0 vs 17.6个月P =0.0011, mPFS: 15.8 vs 9.3个月,P < 0.05)。单因素和多因素分析确定治疗方案是PFS和OS的独立因素。T+L+P方案的安全性是可以接受的。与L+P组相比,T+L+P组不良反应的发生率和严重程度无显著差异(任何级别,90.1 vs 93.6%, P =0.551;≥3级,25.9% vs 23.8%, p=0.843)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.50
自引率
2.40%
发文量
108
审稿时长
16 weeks
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