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不可切除肝细胞癌中分子靶向治疗联合 PD-(L)1 抑制剂加或不加 TACE 的疗效及安全性比较:一项回顾性研究

 

Authors Liu J, Wang Y, Cui L , Nie Y, Li C, Tan W , Li Y, Bai Y, Wan T, Hu B, Liu Z, Hu M, Wang M , Duan F

Received 10 October 2024

Accepted for publication 29 March 2025

Published 17 July 2025 Volume 2025:14 Pages 761—771

DOI https://doi.org/10.2147/ITT.S495451

Checked for plagiarism Yes

Review by Single anonymous peer review

Peer reviewer comments 4

Editor who approved publication: Dr Sarah Wheeler

Jiangtao Liu,1,* Yan Wang,2,* Li Cui,2 Yan Nie,1 Chao Li,1 Wenle Tan,2 Ye Li,1 Yanhua Bai,1 Tao Wan,3 Bingyang Hu,3 Zhe Liu,3 Minggen Hu,3 Maoqiang Wang,2 Feng Duan2 

1Department of Gastroenterology, Hainan Hospital of Chinese People’s Liberation Army (PLA) General Hospital, Sanya, Hainan, 572000, People’s Republic of China; 2Department of Interventional Radiology, Chinese People’s Liberation Army (PLA) General Hospital, Beijing, 100853, People’s Republic of China; 3Faculty of Hepato-Biliary-Pancreatic Surgery, Chinese People’s Liberation Army (PLA) General Hospital, Beijing, 100853, People’s Republic of China

*These authors contributed equally to this work

Correspondence: Feng Duan, Email duanfeng@vip.sina.com

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.

Keywords: molecular targeted therapy, PD-(L)1, hepatocellular carcinoma, transarterial chemoembolization