He Zhaoqian, Chen Hua, Liang Chen, Tang Xiang, Jiang Lingmin, Xie Feihu, Liu Qi, Zheng Yun
Department of Liver Surgery, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, 510060, People's Republic of China.
Collaborative Innovation Center for Cancer Medicine, State Key Laboratory of Oncology in South China, Sun Yat-Sen University Cancer Center, Guangzhou, Guangdong, 510060, People's Republic of China.
Immunotargets Ther. 2025 Jan 25;14:51-63. doi: 10.2147/ITT.S502350. eCollection 2025.
To compare the clinical outcomes of different systemic therapies, specifically PD(L)1 inhibitors plus Lenvatinib versus Atezolizumab plus Bevacizumab, when combined with hepatic arterial infusion chemotherapy (HAIC) based on the FOLFOX regimen (oxaliplatin, fluorouracil, and leucovorin) as first line treatment for unresectable hepatocellular carcinoma.
This real-world retrospective study enrolled 294 patients with unresectable HCC. All patients received HAIC in combination with either PD(L)1 inhibitors plus Lenvatinib (PLEN-HAIC) or Atezolizumab plus Bevacizumab (AT-HAIC). Propensity score matching (PSM) was performed to balance patient characteristics. The overall response rate (ORR), progression-free survival (PFS), and overall survival (OS) were compared.
After PSM, 80 and 130 patients received AT-HAIC and PLEN-HAIC, respectively. No significant differences were found in ORR between the AT-HAIC and PLEN-HAIC groups (50.0% vs 40.0% per RECIST, p = 0.202; 60.0% vs 57.7% per mRECIST, p = 0.853). Both groups showed similar disease control rates. Median PFS was 14.3 months for PLEN-HAIC versus 8.8 months for AT-HAIC (p = 0.018). Median OS was significantly better in the PLEN-HAIC group (p = 0.045, both not reached). Subgroup analysis revealed that Lenvatinib showed a better OS compared to Bevacizumab when combined with HAIC and PDL1 inhibitors (p = 0.023).
PLEN-HAIC offers significant survival benefits over AT-HAIC in advanced HCC. Given its remarkable efficacy, PLEN-HAIC could be a promising first-line option for unresectable HCC.
比较不同全身治疗方案的临床疗效,具体为帕博利珠单抗(PD)/纳武利尤单抗(L)1抑制剂联合乐伐替尼与阿替利珠单抗联合贝伐单抗,在基于FOLFOX方案(奥沙利铂、氟尿嘧啶和亚叶酸钙)的肝动脉灌注化疗(HAIC)作为不可切除肝细胞癌一线治疗时的疗效。
这项真实世界回顾性研究纳入了294例不可切除肝癌患者。所有患者均接受HAIC联合PD(L)1抑制剂加乐伐替尼(PLEN-HAIC)或阿替利珠单抗加贝伐单抗(AT-HAIC)治疗。采用倾向评分匹配(PSM)来平衡患者特征。比较总缓解率(ORR)、无进展生存期(PFS)和总生存期(OS)。
PSM后,分别有80例和130例患者接受了AT-HAIC和PLEN-HAIC治疗。AT-HAIC组和PLEN-HAIC组的ORR无显著差异(根据RECIST标准分别为50.0%对40.0%,p = 0.202;根据mRECIST标准分别为60.0%对57.7%,p = 0.853)。两组显示出相似的疾病控制率。PLEN-HAIC组的中位PFS为14.3个月,而AT-HAIC组为8.8个月(p = 0.018)。PLEN-HAIC组的中位OS显著更好(p = 0.045,两者均未达到)。亚组分析显示,乐伐替尼与HAIC和PDL1抑制剂联合使用时,其OS优于贝伐单抗(p = 0.023)。
在晚期肝癌中,PLEN-HAIC比AT-HAIC具有显著的生存优势。鉴于其显著疗效,PLEN-HAIC可能是不可切除肝癌有前景的一线治疗选择。