Wu Qing, Li Ping, Lin Nan, Mao BinBin, Xie Xianhe
Department of Oncology, The First Affiliated Hospital of Fujian Medical University, Fuzhou, Fujian, China.
Department of Oncology, National Regional Medical Center, Binhai Campus of The First Affiliated Hospital, Fujian Medical University, Fuzhou, Fujian, China.
J Immunother. 2025 Oct 1;48(8):314-324. doi: 10.1097/CJI.0000000000000566.
We aimed to investigate the efficacy and safety of transarterial chemoembolization (TACE) or hepatic arterial infusion chemotherapy (HAIC) combined with immune checkpoint inhibitors (ICIs) and angiogenesis inhibitors in unresectable hepatocellular carcinoma (uHCC). The endpoints were the objective response rate (ORR), disease control rate (DCR), conversion rate, progression-free survival (PFS), overall survival (OS), and the incidence of adverse events (AEs). Stratified analyses were accomplished based on local treatment and evaluation criteria. Totally, 4930 individuals from 76 studies were recruited. For initial uHCC treated with the triple therapy, the pooled pathologic complete response (pCR) rate, major pathologic response (MPR) rate, and conversion resection rate were 29.91%, 44.81%, and 30.98%; the ORR and DCR were 38.52% and 84.42% according to RECIST 1.1, 57.82% and 85.82% by mRECIST 1.1. Furthermore, PFS rates at 6-months, 12-months, 18-months, 24-months, and 30-months were 74.77%, 44.30%, 30.97%, 22.71%, and 15.35%; while OS rates at 6-months, 12-months, 18-months, 24-months, 30-months, and 36-months were 94.94%, 76.95%, 58.17%, 45.19%, 27.38%, and 17.79%, respectively. The pooled results showed that the pooled PFS of triple therapy was superior to that of the control group (HR=0.74, 95% CI: 0.71-0.77), so was OS (HR=0.68, 95% CI: 0.65-0.72). The pooled rate of any grade AEs was 91.93%, and grade 3 or higher AEs was 34.50%. There were no fatal AEs reported in any of the included studies. The triple therapy of TACE/HAIC combined with ICIs and angiogenesis inhibitors was promising in uHCC with good efficacy and tolerated toxicity; however, the potential influence of confounding factors cannot be entirely excluded.
我们旨在研究经动脉化疗栓塞术(TACE)或肝动脉灌注化疗(HAIC)联合免疫检查点抑制剂(ICIs)和血管生成抑制剂治疗不可切除肝细胞癌(uHCC)的疗效和安全性。观察终点为客观缓解率(ORR)、疾病控制率(DCR)、转化率、无进展生存期(PFS)、总生存期(OS)和不良事件(AE)发生率。基于局部治疗和评估标准进行分层分析。总共纳入了来自76项研究的4930名个体。对于接受三联疗法治疗的初治uHCC患者,汇总的病理完全缓解(pCR)率、主要病理缓解(MPR)率和转化切除率分别为29.91%、44.81%和30.98%;根据RECIST 1.1标准,ORR和DCR分别为38.52%和84.42%,根据mRECIST 1.1标准分别为57.82%和85.82%。此外,6个月、12个月、18个月、24个月和30个月时的PFS率分别为74.77%、44.30%、30.97%、22.71%和15.35%;而6个月、12个月、18个月、24个月、30个月和36个月时的OS率分别为94.94%、76.95%、58.17%、45.19%、27.38%和17.79%。汇总结果显示,三联疗法的汇总PFS优于对照组(HR = 0.74,95%CI:0.71 - 0.77),OS也是如此(HR = 0.68,95%CI:0.65 - 0.72)。任何级别AE的汇总发生率为91.93%,3级及以上AE为34.50%。纳入的任何研究中均未报告致命AE。TACE/HAIC联合ICIs和血管生成抑制剂的三联疗法在uHCC治疗中前景良好,疗效佳且毒性可耐受;然而,混杂因素的潜在影响不能完全排除。