Sun Xuqi, Zhang Qi, Mei Jie, Yang Ziliang, Chen Minshan, Liang Tingbo
Department of Hepatobiliary and Pancreatic Surgery, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310006, China.
Zhejiang Provincial Key Laboratory of Pancreatic Disease, the First Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.
BMC Cancer. 2022 Mar 19;22(1):293. doi: 10.1186/s12885-022-09405-7.
This study aimed to evaluate the efficiency and prognostic factors of lenvatinib plus programmed death 1 (PD-1) blockades in patients with advanced hepatocellular carcinoma (HCC), especially for those with tumor occupation ≥50% volume of liver (TO ≥50%) or invasion in Vp4, who were excluded from the trial KEYNOTE-524.
We reviewed the clinical data of patients with unresectable HCC who received lenvatinib plus PD-1 blockades. The Kaplan-Meier method was performed to compare the progression-free survival (PFS) and the overall survival (OS). Cox proportional hazards model was adopted to identify independent prognostic factors.
The median PFS and OS of the enrolled 84 HCC patients (31 patients with TO ≥50% and 30 patients with Vp4 invasion) were 6.6 and 11.4 months respectively. TO ≥50% had significantly negative impact on the objective response rates (ORR) (p = 0.015). HCC patients with TO ≥50% had significantly worse PFS and OS than those with TO < 50% (both p value < 0.001). Conversely, invasion in Vp4 did not significantly affect the ORR, PFS or OS for HCC patients receiving lenvatinib plus PD-1 blockades (p = 0.419, 0.528 and 0.855). After multivariate analyses, TO ≥50% was the independent predictor for PFS and OS (both p value < 0.001). No significant correlation was found between any kind of AEs and TO ≥50% or invasion in Vp4.
Lenvatinib plus PD-1 blockades can provide survival benefits for HCC patients with invasion in Vp4 and the indications of lenvatinib plus pembrolizumab may be further expanded. Locoregional treatments should be considered for patients with TO ≥50% during systemic therapy.
本研究旨在评估乐伐替尼联合程序性死亡受体1(PD-1)阻断剂治疗晚期肝细胞癌(HCC)患者的疗效及预后因素,尤其针对那些肿瘤占据肝脏体积≥50%(TO≥50%)或侵犯Vp4而被排除在KEYNOTE-524试验之外的患者。
我们回顾了接受乐伐替尼联合PD-1阻断剂治疗的不可切除HCC患者的临床资料。采用Kaplan-Meier法比较无进展生存期(PFS)和总生存期(OS)。采用Cox比例风险模型确定独立预后因素。
纳入的84例HCC患者(31例TO≥50%,30例Vp4侵犯)的中位PFS和OS分别为6.6个月和11.4个月。TO≥50%对客观缓解率(ORR)有显著负面影响(p = 0.015)。TO≥50%的HCC患者的PFS和OS明显差于TO<50%的患者(p值均<0.001)。相反,Vp4侵犯对接受乐伐替尼联合PD-1阻断剂治疗的HCC患者的ORR、PFS或OS无显著影响(p = 0.419、0.528和0.855)。多因素分析后,TO≥50%是PFS和OS的独立预测因素(p值均<0.001)。未发现任何不良事件与TO≥50%或Vp4侵犯之间存在显著相关性。
乐伐替尼联合PD-1阻断剂可为Vp4侵犯的HCC患者带来生存获益,乐伐替尼联合派姆单抗的适应证可能会进一步扩大。对于TO≥50%的患者,在全身治疗期间应考虑局部治疗。