Xiao Yadi, Tao Xiangbo, Zhang Haitao, Shi Xin, Zhao Hongjian
Departments of Oncology.
Pathology.
Eur J Gastroenterol Hepatol. 2025 Sep 1;37(9):993-1002. doi: 10.1097/MEG.0000000000003012. Epub 2025 Jun 6.
The safety and therapeutic efficiency of tyrosine kinase inhibitors (TKIs) and programmed death-1 (PD-1) inhibitors in combination with hepatic artery infusion chemotherapy (HAIC) for patients with unresectable/advanced hepatocellular carcinoma (HCC) require further investigation. This meta-analysis aimed to thoroughly investigate the safety and efficacy of this triple combination therapy based on currently available research. PubMed, Embase, Cochrane Library, Web of Science, VIP, Wan Fang, and China National Knowledge Infrastructure were searched. Outcomes included complete response (CR), partial response (PR), stable disease, overall survival, progression-free survival, and treatment/laboratory-related adverse events. Stata15.1 software was used for random/fixed-effect model analysis. Ten studies with 1108 patients were incorporated in the analysis. For efficacy, the triple combination therapy achieved an improved CR rate [relative risk (RR): 2.76, 95% confidence interval (CI): 1.43-5.33] and PR rate (RR: 1.70, 95% CI: 1.01-2.86) than the control group. Moreover, the triple combination therapy decreased the 44% risk of death [hazard ratio (HR): 0.56, 95% CI: 0.46-0.67] and 37% risk of disease progression (HR: 0.63, 95% CI: 0.53-0.75) compared with the control group. The triple combination therapy group and the control group did not exhibit a statistical difference in treatment- or laboratory-related adverse events. In the management of unresectable/advanced HCC, HAIC in conjunction with PD-1 inhibitors and TKI exhibits both safety and efficacy, providing a scientific basis for clinical practice.
酪氨酸激酶抑制剂(TKIs)和程序性死亡-1(PD-1)抑制剂联合肝动脉灌注化疗(HAIC)用于不可切除/晚期肝细胞癌(HCC)患者的安全性和治疗效果尚需进一步研究。本荟萃分析旨在根据现有研究全面调查这种三联疗法的安全性和疗效。检索了PubMed、Embase、Cochrane图书馆、科学网、维普、万方和中国知网。结局指标包括完全缓解(CR)、部分缓解(PR)、疾病稳定、总生存期、无进展生存期以及治疗/实验室相关不良事件。使用Stata15.1软件进行随机/固定效应模型分析。纳入分析的有10项研究,共1108例患者。在疗效方面,三联疗法的CR率[相对危险度(RR):2.76,95%置信区间(CI):1.43 - 5.33]和PR率(RR:1.70,95%CI:1.01 - 2.86)均高于对照组。此外,与对照组相比,三联疗法降低了44%的死亡风险[风险比(HR):0.56,95%CI:0.46 - 0.67]和37%的疾病进展风险(HR:0.63,95%CI:0.53 - 0.75)。三联疗法组和对照组在治疗或实验室相关不良事件方面未显示出统计学差异。在不可切除/晚期HCC的治疗中,HAIC联合PD-1抑制剂和TKI兼具安全性和有效性,为临床实践提供了科学依据。