Efficacy and safety of anti-PD-1 monotherapy versus anti-PD-1 antibodies plus lenvatinib in patients with advanced hepatocellular carcinoma: a real-world experience

被引:4
|
作者
Liu, Qingyan [3 ,4 ]
Li, Rong [5 ]
Li, Lingling [6 ]
Wang, Gaokun [7 ]
Ji, Shiyu [3 ]
Zheng, Xuan [3 ]
Jia, Xiaodong [2 ]
Tao, Haitao [1 ]
Hu, Yi [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 5, Dept Oncol, 28 Fuxing Rd, Beijing 100000, Peoples R China
[2] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 5, Dept Oncol, 100 West Fourth Ring Rd, Beijing 100039, Peoples R China
[3] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 5, Dept Oncol, Beijing, Peoples R China
[4] Med Sch Chinese Peoples Liberat Army, Beijing, Peoples R China
[5] Chinese Peoples Liberat Army Gen Hosp, Med Ctr 2, Dept Hlth Med, Beijing, Peoples R China
[6] Shanghai Jiao Tong Univ, Renji Hosp, Sch Med, Dept Oncol, Shanghai, Peoples R China
[7] Changchun Second Cadre Rest Ctr Jilin Prov Mil Reg, Changchun, Jilin, Peoples R China
关键词
anti-PD-1; combination therapy; hepatocellular carcinoma; immune checkpoint inhibitors; lenvatinib; OPEN-LABEL; SORAFENIB; PEMBROLIZUMAB; BEVACIZUMAB;
D O I
10.1177/17588359231206274
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The efficacy of anti-programmed cell death (PD)-1 monotherapy in advanced hepatocellular carcinoma (aHCC) is limited, and combination therapy with lenvatinib and pembrolizumab has shown promising results. However, comparative studies between immune monotherapies and combination therapies are lacking.Objectives: To investigate the efficacy and safety of anti-PD-1 monotherapy (PD-1) and anti-PD-1 plus lenvatinib (PD-1 + L) in patients with aHCC to guide clinical treatment decisions.Design: A retrospective study was conducted on a cohort of patients with aHCC who received either PD-1 monotherapy or PD-1 + L combination therapy between January 2018 and January 2020.Methods: The study retrospectively reviewed the medical records of 94 eligible patients with aHCC, with 39 in the PD-1 group and 55 in the PD-1 + L group. The efficacy outcomes, including objective response rate (ORR), disease control rate (DCR), duration of response (DOR), progression-free survival (PFS), overall survival (OS), and safety, were assessed.Results: With a median follow-up of 30.1 months, the PD-1 + L group demonstrated a significantly higher ORR (32.7% versus 10.3%, p = 0.013), better DCR (80.0% versus 53.8%, p = 0.012), longer median PFS (10.6 versus 4.4 months, p < 0.001) and longer median OS (18.4 versus 8.5 months, p = 0.013) than PD-1 group. For the responders, the efficacy of the two groups was durable (DOR was 11.6 versus 3.5 months, p = 0.009). Subgroup analyses based on prior tyrosine kinase inhibitor (TKI) treatment and the presence or absence of macrovascular tumor thrombosis or extrahepatic metastases favored the PD-1 + L group. The combination therapy was a good predictor of PFS and OS in multivariate analysis. Grade 3/4 treatment-related adverse events were more common in PD-1 + L group, with higher incidences of hypertension and hand-foot skin reactions.Conclusions: PD-1 monotherapy and PD-1 plus lenvatinib combination therapy were well-tolerated in patients with aHCC. PD-1 + L showed significantly better survival benefits than PD-1 monotherapy.
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页数:15
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