Efficacy and Safety of Transarterial Chemoembolization Plus Donafenib with or without Immune Checkpoint Inhibitors as the First-Line Treatment for Unresectable Hepatocellular Carcinoma: A Propensity Score Matching Analysis

被引:1
|
作者
Deng, Liwei [1 ,2 ]
Sun, Yanyuan [2 ]
Wang, Haiqing [3 ]
Liao, Changli [2 ]
Li, Deshan [2 ]
Xu, Guohui [2 ]
Yang, Xuegang [2 ]
机构
[1] Univ Elect Sci & Technol China, Sch Med, Chengdu, Peoples R China
[2] Sichuan Canc Ctr, Sichuan Canc Hosp & Inst, Dept Intervent Therapy, 55 Renmin South Rd 4th Sect, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Canc Ctr, Dept Hepatobiliary Pancreat Surg, Sichuan Canc Hosp & Inst, Chengdu, Peoples R China
关键词
unresectable hepatocellular carcinoma; transarterial chemoembolization; donafenib; immune checkpoint inhibitor; combined therapy; OPEN-LABEL; BEVACIZUMAB; SORAFENIB;
D O I
10.2147/JHC.S443779
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: To compare the efficacy and safety of transarterial chemoembolization (TACE) plus donafenib with immune checkpoint inhibitors (ICIs) (T+D+I) versus TACE plus donafenib (T+D) as the first-line treatment for patients with unresectable hepatocellular Methods: This retrospective study included patients with unresectable HCC who received T+D+I or T+D between June 2021 and February 2023. The tumor response was analyzed according to the modified Response Evaluation Criteria in Solid Tumors. The objective response rate (ORR), disease control rate (DCR), progression-free survival (PFS), overall survival (OS), and treatmentrelated adverse events (TRAEs) in the two groups were compared before and after propensity score matching (PSM). Cox's proportional-hazards regression model was used to analyze factors affecting PFS and OS. Results: This study included 69 patients: 41 patients in the T+D group and 28 patients in the T+D+I group. After PSM, 26 patients in each group were analyzed. Patients in the T+D+I group had a higher DCR (96.2% vs 73.1%, P = 0.021), longer median PFS (13.1 vs 7.2 months, P = 0.017), and longer median OS (23.1 vs 14.7 months, P = 0.021) than those in the T+D group. The ORR in the two groups was similar (53.8% vs 50.0%, P = 0.781). Multivariate analyses revealed that T+D+I treatment and total bilirubin levels of <20 mu mol/L were independent prognostic factors for long PFS. T+D+I treatment, Child-Pugh class A, and single-lobe tumor distribution were independent prognostic factors for long OS. The incidence of TRAEs in the two groups was similar (P > 0.05). Conclusion: In comparison with TACE plus donafenib, TACE plus donafenib with ICIs could significantly improve DCR, PFS, and OS as a potential first-line treatment for unresectable HCC with an acceptable safety profile.
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收藏
页码:29 / 38
页数:10
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