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.

IF 4.2 3区 医学 Q2 ONCOLOGY Journal of Hepatocellular Carcinoma Pub Date : 2024-08-24 eCollection Date: 2024-01-01 DOI:10.2147/JHC.S472286
Jiayun Jiang, Hui Zhang, Jiejuan Lai, Shiyu Zhang, Yanjiao Ou, Yu Fu, Leida Zhang
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Abstract

Purpose: To compare the efficacy and safety of transarterial chemoembolization (TACE) plus lenvatinib and tislelizumab (TACE-Len-T) versus TACE plus lenvatinib (TACE-Len) as the first-line treatment for patients with unresectable hepatocellular carcinoma (uHCC).

Patients and methods: This retrospective study included 136 uHCC patients treated with TACE-Len-T or TACE-Len from January 1, 2021, to June 30, 2023. Clinical outcomes including overall survival (OS), progression-free survival (PFS), tumor response and adverse events (AEs) were compared between the two groups. The risk factors affecting OS and PFS were also analyzed.

Results: The median OS and PFS of the TACE-Len-T group were significantly longer than those of the TACE-Len group (Median OS: not reached vs 13.8 months, P<0.001; Median PFS: 13.0 months vs 2.7 months, P<0.001). The best overall objective response rate (ORR) was also better with TACE-Len-T treatment (ORR: 72.1% vs 29.4%, P<0.001), and the disease control rate (DCR) significantly increased in the TACE-Len-T group (88.2% vs 48.5%, P<0.001). Multivariate analyses revealed that TACE-Len treatment, tumor number >3, and cTACE were independent risk factors for OS, whereas TACE-Len treatment was the only independent risk factor for PFS. The frequency and severity of AEs in the TACE-Len-T group were comparable to those in the TACE-Len group (any grade: 92.6% vs 91.2%, P=0.753; grade 3 or 4: 33.8% vs 32.3%, P=0.855).

Conclusion: TACE-Len-T treatment significantly improved OS, PFS, ORR, and DCR over TACE-Len treatment, with a manageable safety profile in uHCC.

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经动脉化疗栓塞加仑伐替尼联合或不联合替舒瑞珠单抗作为不可切除肝细胞癌一线治疗的有效性和安全性:倾向得分匹配分析。
目的:比较经动脉化疗栓塞(TACE)加来伐替尼和替舒瑞单抗(TACE-Len-T)与TACE加来伐替尼(TACE-Len)作为不可切除肝细胞癌(uHCC)患者一线治疗的疗效和安全性:这项回顾性研究纳入了2021年1月1日至2023年6月30日期间接受TACE-Len-T或TACE-Len治疗的136例uHCC患者。比较了两组患者的临床结局,包括总生存期(OS)、无进展生存期(PFS)、肿瘤反应和不良事件(AEs)。此外,还分析了影响OS和PFS的风险因素:结果:TACE-Len-T组的中位OS和PFS明显长于TACE-Len组(中位OS:未达到vs 13.8个月,P3,cTACE是OS的独立危险因素,而TACE-Len治疗是PFS的唯一独立危险因素)。TACE-Len-T组的AEs频率和严重程度与TACE-Len组相当(任何等级:92.6% vs 91.2%,P=0.753;3级或4级:33.8% vs 32.3%,P=0.855):结论:与TACE-Len治疗相比,TACE-Len-T治疗可明显改善uHCC的OS、PFS、ORR和DCR,且安全性可控。
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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
期刊最新文献
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