Efficacy and Safety of Lenvatinib Plus Programmed Death-1 Inhibitors with or Without Transarterial Chemoembolization in the Treatment of Unresectable Hepatocellular Carcinoma

被引:1
作者
Jin, Ming [1 ]
Jiang, Zhi-qing [2 ]
Qin, Jia-hui [3 ]
Qin, Hui-xia [4 ]
Jiang, Kai-wen [3 ]
Ya, Hou-xiang [3 ]
Gu, Jing [3 ]
Gui, Mo-rui [5 ]
Li, Yao-hua [3 ]
Xu, Long-kuan [6 ]
Fu, Hai-xiao [6 ]
Xiao, Xu-hua [7 ]
Li, Shu-qun [3 ]
机构
[1] Guilin Med Univ, Affiliated Hosp, Dept Vasc Intervent, Guilin, Guangxi, Peoples R China
[2] Guilin Med Univ, Affiliated Hosp, Dept Gastrointestinal Surg, Guilin, Guangxi, Peoples R China
[3] Guilin Med Univ, Affiliated Hosp, Dept Hepatobiliary Pancreat Surg, Guilin, Guangxi, Peoples R China
[4] Guilin Med Univ, Affiliated Hosp, Intervent Ctr, Guilin, Guangxi, Peoples R China
[5] Guilin Med Univ, Affiliated Hosp, Med Aesthet Surg, Dept Burn Wound Repair & Plast Surg, Guilin, Guangxi, Peoples R China
[6] Guilin Med Univ, Affiliated Hosp, Dept Pathol, Guilin, Guangxi, Peoples R China
[7] Guilin Med Univ, Affiliated Hosp, Dept Gastroenterol, Guilin, Guangxi, Peoples R China
关键词
unresectable hepatocellular carcinoma; lenvatinib; transarterial chemoembolization; PD-1; inhibitor; combination therapy; propensity score matching; 1ST-LINE TREATMENT; OPEN-LABEL; SORAFENIB; MULTICENTER; BEVACIZUMAB; MANAGEMENT; THERAPY;
D O I
10.2147/JHC.S485047
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: Transarterial chemoembolization (TACE) is recommended as a standard therapy for intermediate-stage hepatocellular carcinoma (HCC) and is the most widely used first-line treatment for advanced HCC. This study aimed to evaluate the clinical benefits and tolerability of TACE added to a combination of lenvatinib and programmed death-1 (PD-1) inhibitor in patients with unresectable HCC (uHCC). Patients and Methods: We conducted a retrospective cohort study involving 144 patients with uHCC treated between August 2020 and August 2023. Patients received a combination of lenvatinib and a PD-1 inhibitor with or without TACE (T+L+P, n=81 or L+P, n=63, respectively). The baseline characteristics of the two groups were compared, and propensity score matching (PSM) was used to minimize bias. The study endpoints included overall survival (OS), progression-free survival (PFS), and objective response rate (ORR). Factors influencing survival rates were analyzed using Cox regression, and adverse events (AEs) were documented and assessed. Results: Before PSM, the T+L+P group showed significantly higher ORR (64.1% vs 44.4%, p < 0.05), longer median PFS (14.3 vs 9.6 months, p < 0.05), and longer median OS (24.6 vs 19.5 months, p < 0.05) compared to the L+P group. Even post-PSM, the T+L+P group showed significantly better OS and PFS compared to the L+P group (mOS: 28.0 vs 17.6 months p=0.0011, mPFS: 15.8 vs 9.3 months, p < 0.05). Univariate and multivariate analyses identified treatment options as independent factors for PFS and OS. The safety profile of the T+L+P regimen was acceptableThe incidence and severity of adverse reactions in the T+L+P group were not significantly different compared to the L+P group (any grade, 90.1 vs 93.6%, p=0.551; grade >= 3, 25.9 vs 23.8%, p=0.843).
引用
收藏
页码:2309 / 2320
页数:12
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