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分子靶向治疗联合PD-(L)1加或不加经动脉化疗栓塞术治疗不可切除肝细胞癌的疗效与安全性比较:一项回顾性研究

Comparative Effectiveness and Safety of Molecular Targeted Therapy Plus PD-(L)1 with or without TACE in Unresectable Hepatocellular Carcinoma: A Retrospective Study.

作者信息

Liu Jiangtao, Wang Yan, Cui Li, Nie Yan, Li Chao, Tan Wenle, Li Ye, Bai Yanhua, Wan Tao, Hu Bingyang, Liu Zhe, Hu Minggen, Wang Maoqiang, Duan Feng

机构信息

Department of Gastroenterology, Hainan Hospital of Chinese People's Liberation Army (PLA) General Hospital, Sanya, Hainan, 572000, People's Republic of China.

Department of Interventional Radiology, Chinese People's Liberation Army (PLA) General Hospital, Beijing, 100853, People's Republic of China.

出版信息

Immunotargets Ther. 2025 Jul 17;14:761-771. doi: 10.2147/ITT.S495451. eCollection 2025.

Abstract

OBJECTIVE

This study aims to compare the effectiveness and safety of TACE combined with molecular targeted therapy (MTT) plus Programmed death-ligand 1 (PD-(L)1) antibodies versus MTT plus PD-(L)1 antibodies for HCC patients.

METHODS

Data from HCC patients who received either MTT plus PD-(L)1 (systemic therapy group) or TACE combined with MTT plus PD-(L)1 (combination therapy group) were retrospectively analyzed. The primary outcome was the objective reaction rate (ORR) at the initial assessment post-treatment initiation. Secondary outcomes included progressive free survival (PFS), overall survival (OS) and grade-3 or higher adverse events.

RESULTS

A total of 222 HCC patients were included (109 in the systemic therapy group, 113 in the combination therapy group). Propensity score matching yielded 80 patients per group. The odds ratio for ORR in the combination therapy group was 1.29 (95% CI: 0.64-2.60; p=0.479). Subgroup analysis revealed significantly higher ORR for patients with AFP≤200 ng/mL in the combination therapy group (OR=3.54, p=0.016). For patients without PVTT, the ORR odds were slightly higher with combination therapy (OR=5.33, p=0.068). Multivariate Cox regression analysis showed no significant differences in PFS (HR=0.68, p=0.131) or OS (HR=0.86, p=0.674) between the two groups. Higher baseline AFP (>200 ng/mL) was associated with worse PFS (HR=1.68, p=0.012) and OS (HR=2.33, p=0.021). Surgical resection improved PFS (HR=0.42, p<0.001) and OS (HR=0.31, p=0.004). Grade 3 or higher adverse events were more common in the combination therapy group (52% vs 15%, p<0.0001).

CONCLUSION

No significant benefits were observed for combining TACE with MTT and PD-(L)1 in unresectable HCC patients. However, TACE may offer advantages for patients with AFP≤200 ng/mL or without PVTT.

摘要

目的

本研究旨在比较经动脉化疗栓塞术(TACE)联合分子靶向治疗(MTT)加程序性死亡配体1(PD-(L)1)抗体与MTT加PD-(L)1抗体治疗肝癌患者的有效性和安全性。

方法

回顾性分析接受MTT加PD-(L)1(全身治疗组)或TACE联合MTT加PD-(L)1(联合治疗组)的肝癌患者数据。主要结局是治疗开始后初次评估时的客观缓解率(ORR)。次要结局包括无进展生存期(PFS)、总生存期(OS)和3级或更高等级不良事件。

结果

共纳入222例肝癌患者(全身治疗组109例,联合治疗组113例)。倾向评分匹配后每组80例患者。联合治疗组ORR的优势比为1.29(95%置信区间:0.64-2.60;p=0.479)。亚组分析显示,联合治疗组中AFP≤200 ng/mL的患者ORR显著更高(OR=3.54,p=0.016)。对于无门静脉癌栓(PVTT)的患者,联合治疗的ORR优势比略高(OR=5.33,p=0.068)。多因素Cox回归分析显示,两组之间的PFS(HR=0.68,p=0.131)或OS(HR=0.86,p=0.674)无显著差异。较高的基线AFP(>200 ng/mL)与较差的PFS(HR=1.68,p=0.012)和OS(HR=2.33,p=0.021)相关。手术切除可改善PFS(HR=0.42,p<0.001)和OS(HR=0.31,p=0.004)。3级或更高等级不良事件在联合治疗组中更常见(52%对15%,p<0.0001)。

结论

在不可切除的肝癌患者中,未观察到TACE联合MTT和PD-(L)1有显著益处。然而,TACE可能对AFP≤200 ng/mL或无PVTT的患者具有优势。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/68b3/12278979/7a28ac59b23e/ITT-14-761-g0001.jpg

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