Yu Jiahui, Yu Jinxin, Chen Yimiao, Yang Yuting, Yi Pengsheng
Department of Hepato-Biliary-Pancrease II, Affiliated Hospital of North Sichuan Medical College, Nanchong, Sichuan, 637000, People's Republic of China.
North Sichuan Medical College, Nanchong, Sichuan, 637000, People's Republic of China.
BMC Cancer. 2025 Mar 28;25(1):564. doi: 10.1186/s12885-025-13932-4.
The efficacy of adding programmed death-1 (PD-1) inhibitors to transcatheter arterial chemoembolization (TACE) combined with apatinib for advanced hepatocellular carcinoma (HCC) remains controversial. This study aimed to evaluate the efficacy of incorporating PD-1 inhibitors into TACE combined with apatinib.
Relevant literature on TACE combined with apatinib plus PD-1 inhibitors for advanced HCC was searched in PubMed, Cochrane Library, Embase, and Web of Science databases. Trial sequential analysis (TSA) was conducted to minimize randomization errors and assess whether the meta-analysis provided conclusive evidence.
Six studies involving 1,452 patients were included. Compared with the TACE combined with apatinib treatment group (T-A), TACE combined with apatinib plus PD-1 inhibitors (T-A-P) significantly prolonged overall survival (OS) (Hazard Ratio [HR] 2.22, 95% Confidence Interval [CI] 1.93-2.56; p < 0.001) and progression-free survival (PFS) (HR 2.36, 95% CI 2.01-2.77; p < 0.001), while also improving the objective response rate (ORR) (risk ratios [RR] 1.60, 95% CI 1.20-2.14; p < 0.001) and disease control rate (DCR) (RR 1.06, 95% CI 1.00-1.12; p < 0.001). TSA results indicated that additional studies were required to confirm the significance of DCR. Prognostic analysis identified treatment regimen and extrahepatic metastasis as common independent risk factors for OS and PFS. The incidence of adverse events in the T-A-P treatment group was comparable to that in the T-A treatment group.
Adding PD-1 inhibitors to TACE combined with apatinib significantly prolonged OS and PFS, particularly in patients without extrahepatic metastases. It also improved ORR and DCR in patients with HCC.
对于晚期肝细胞癌(HCC),在经动脉化疗栓塞术(TACE)联合阿帕替尼的基础上加用程序性死亡-1(PD-1)抑制剂的疗效仍存在争议。本研究旨在评估将PD-1抑制剂纳入TACE联合阿帕替尼治疗中的疗效。
在PubMed、Cochrane图书馆、Embase和Web of Science数据库中检索关于TACE联合阿帕替尼加PD-1抑制剂治疗晚期HCC的相关文献。进行试验序贯分析(TSA)以尽量减少随机误差,并评估荟萃分析是否提供了确凿的证据。
纳入了6项涉及1452例患者的研究。与TACE联合阿帕替尼治疗组(T-A)相比,TACE联合阿帕替尼加PD-1抑制剂(T-A-P)显著延长了总生存期(OS)(风险比[HR] 2.22,95%置信区间[CI] 1.93 - 2.56;p < 0.001)和无进展生存期(PFS)(HR 2.36,95% CI 2.01 - 2.77;p < 0.001),同时还提高了客观缓解率(ORR)(风险比[RR] 1.60,95% CI 1.20 - 2.14;p < 0.001)和疾病控制率(DCR)(RR 1.06,95% CI 1.00 - 1.12;p < 0.001)。TSA结果表明,需要更多研究来证实DCR的显著性。预后分析确定治疗方案和肝外转移是OS和PFS常见的独立危险因素。T-A-P治疗组的不良事件发生率与T-A治疗组相当。
在TACE联合阿帕替尼的基础上加用PD-1抑制剂可显著延长OS和PFS,尤其是对于无肝外转移的患者。它还提高了HCC患者的ORR和DCR。