Efficacy and Safety of Transarterial Chemoembolization Combined with PD-1 Inhibitors plus Molecular Targeted Therapies for Unresectable Hepatocellular Carcinoma with Child‒Pugh B

Author:

Huang Jin-Tao1,Hong Xin2,Hu Di1,Zhou Wen-Jie3,Yang Hao1,Shen Jian1,Lv Peng-Hua3,Yang Zheng-Qiang4,Zhu Xiao-Li1

Affiliation:

1. The First Affiliated Hospital of Soochow University

2. Affiliated Hospital 2 of Nantong University

3. Northern Jiangsu People's Hospital, Clinical Medical College of Yangzhou University

4. National Cancer Center, Chinese Academy of Medical Sciences and Peking Union Medical College

Abstract

Abstract

Background and Objectives To assess the efficacy and safety of transarterial chemoembolization (TACE) combined with programmed cell death-1 (PD-1) inhibitors plus molecular targeted therapies (MTT) for unresectable hepatocellular carcinoma (HCC) with Child-Pugh (CP)-B (score of 7-8). Methods This multicenter retrospective study enrolled patients with unresectable HCC receivingTACE combined with PD-1 inhibitors plus MTT between January 2019 and December 2022. Propensity score matching (PSM) was performed to reduce bias between the CP-A and CP-B (score of 7-8) groups. The primary outcome was overall survival (OS)and the secondary outcomes included progression-free survival (PFS), objective response rate (ORR), disease control rate (DCR), and adverse events (AEs). Results A total of 416 patients were ultimately included in the study. The median OS was 26.4 months (95% CI, 22.7-30.0) for the overall population during a median follow-up period of 32.5 months. The median OS was greater in patients with CP-A liver function than in patients with CP-B (score of 7-8), but the difference was not statistically significant. After PSM, the OS, PFS, ORR, and DCR of CP-A patients were comparable to those of CP-B (score of 7-8) patients. No significant difference was observed in the incidence of grade 3/4 AEs between the two groups. Conclusions Unresectable HCC patients with CP-B (score of 7-8) undergoing TACE combined with PD-1 inhibitors plus MTT showed similar clinical activity and safety profiles compared to CP-A patients.

Publisher

Springer Science and Business Media LLC

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