[TACE-HAIC versus HAIC combined with targeted immunotherapy for unresectable hepatocellular carcinoma: a propensity score-matched retrospective controlled study].
{"title":"[TACE-HAIC versus HAIC combined with targeted immunotherapy for unresectable hepatocellular carcinoma: a propensity score-matched retrospective controlled study].","authors":"C Liu, M Zhao, J Li, K Zhao, L Zheng, J C Xiao","doi":"10.3760/cma.j.cn501113-20250920-00399","DOIUrl":null,"url":null,"abstract":"<p><p><b>Objective:</b> To investigate the safety profile and efficacy of transarterial chemoembolization (TACE)-hepatic arterial infusion chemotherapy (HAIC) and HAIC combined with targeted immunotherapy in patients with unresectable hepatocellular carcinoma (uHCC). <b>Methods:</b> Clinical data of patients with uHCC who received TACE-HAIC or HAIC as the initial local therapy from January 2020 to December 2023 were retrospectively analyzed. Propensity score matching (PSM) was used to compare tumor response, progression-free survival (PFS), overall survival (OS), and adverse events between the two groups. Univariate and multivariate analyses of survival were performed using <i>t</i>-tests, <i>χ</i>² tests, Kaplan-Meier curves, or Cox proportional hazards models, according to the varied data. <b>Results:</b> A total of 258 cases were included, with 41 in the HAIC group and 217 in the TACE-HAIC group. Forty-one matched pairs of patients after PSM (<i>n</i>=41 in the HAIC group and <i>n</i>=82 in the TACE-HAIC group) were obtained. The results showed that the objective response rate (ORR) (70.7% vs. 51.2%, <i>P</i>=0.033) and the disease control rate (90.2% vs. 75.6%, <i>P</i>=0.030) were significantly superior in the TACE-HAIC group than in the HAIC group. The PFS (median 12.7 months vs. 7.9 months, <i>P</i>=0.006) and OS (median 24.4 months vs. 18.9 months, <i>P</i>=0.039) were also significantly prolonged in the TACE-HAIC group. There was no statistically significant difference in the incidence of grade 3/4 adverse events between the two groups. <b>Conclusion:</b> Compared with HAIC combined with targeted immunotherapy, TACE-HAIC combined with targeted immunotherapy shows superior tumor control and survival benefits in uHCC, with a favorable safety profile.</p>","PeriodicalId":24006,"journal":{"name":"中华肝脏病杂志","volume":"34 9","pages":"858-867"},"PeriodicalIF":0.0000,"publicationDate":"2026-09-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC13649362/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"中华肝脏病杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3760/cma.j.cn501113-20250920-00399","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Objective: To investigate the safety profile and efficacy of transarterial chemoembolization (TACE)-hepatic arterial infusion chemotherapy (HAIC) and HAIC combined with targeted immunotherapy in patients with unresectable hepatocellular carcinoma (uHCC). Methods: Clinical data of patients with uHCC who received TACE-HAIC or HAIC as the initial local therapy from January 2020 to December 2023 were retrospectively analyzed. Propensity score matching (PSM) was used to compare tumor response, progression-free survival (PFS), overall survival (OS), and adverse events between the two groups. Univariate and multivariate analyses of survival were performed using t-tests, χ² tests, Kaplan-Meier curves, or Cox proportional hazards models, according to the varied data. Results: A total of 258 cases were included, with 41 in the HAIC group and 217 in the TACE-HAIC group. Forty-one matched pairs of patients after PSM (n=41 in the HAIC group and n=82 in the TACE-HAIC group) were obtained. The results showed that the objective response rate (ORR) (70.7% vs. 51.2%, P=0.033) and the disease control rate (90.2% vs. 75.6%, P=0.030) were significantly superior in the TACE-HAIC group than in the HAIC group. The PFS (median 12.7 months vs. 7.9 months, P=0.006) and OS (median 24.4 months vs. 18.9 months, P=0.039) were also significantly prolonged in the TACE-HAIC group. There was no statistically significant difference in the incidence of grade 3/4 adverse events between the two groups. Conclusion: Compared with HAIC combined with targeted immunotherapy, TACE-HAIC combined with targeted immunotherapy shows superior tumor control and survival benefits in uHCC, with a favorable safety profile.