Combined transarterial chemoembolization and tislelizumab for patients with unresectable hepatocellular carcinoma

被引:0
作者
Tan, Bin-Bin [1 ]
Fu, Ying [2 ]
Shao, Ming-Hua [1 ]
Chen, Hai-Lei [1 ]
Liu, Ping [2 ]
Fan, Chao [2 ]
Zhang, Hui [1 ]
机构
[1] Third Mil Med Univ, Army Med Univ, Affiliated Hosp 1, Dept Hepatobiliary Surg, 30 Gaotanyan Main St, Chongqing 400038, Peoples R China
[2] Third Mil Med Univ, Army Med Univ, Affiliated Hosp 1, Dept Hepatobiliary Surg, Jiangbei Area,958th Hosp Chinese Peoples Liberat A, Chongqing 400020, Peoples R China
来源
WORLD JOURNAL OF GASTROINTESTINAL SURGERY | 2024年 / 16卷 / 09期
关键词
Hepatocellular carcinoma; Transarterial chemoembolization; Therapeutic; Immunotherapy; Prognosis; EFFICACY; SAFETY; BEVACIZUMAB; PLUS;
D O I
10.4240/wjgs.v16.i9.2829
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
BACKGROUND Hepatocellular carcinoma (HCC) often presents as unresectable, necessitating effective treatment modalities. Combining transarterial chemoembolization (TACE) with immunotherapy and targeted therapy has shown promise, yet real-world evidence is needed. AIM To investigate effectiveness and safety of TACE with tislelizumab +/- targeted therapy for unresectable HCC in real-world setting. METHODS This retrospective study included patients with unresectable HCC receiving combined treatment of TACE and tislelizumab. The clinical outcomes included progression-free survival (PFS), overall survival (OS), objective response rate (ORR), and disease control rate (DCR). All patients were evaluated according to the mRECIST criteria. The adverse event (AE) was also assessed. RESULTS In this study of 56 patients with median follow-up of 10.9 months, 7 had previous immunotherapy. Tislelizumab was administered before TACE in 21 (37.50%) and after in 35 (62.50%) patients, with 91.07% receiving concurrent targeted therapy. Median PFS was 14.0 (95%CI: 7.0-18.00) months, and OS was 28 (95%CI: 2.94-53.05) months. Patients with prior immunotherapy had shorter PFS (6 vs. 18 months, P = 0.006). Overall ORR and DCR were 82.14% and 87.50%. Grade >= 3 treatment-related AEs included increased alanine aminotransferase (8.93%), aspartate aminotransferase (10.71%), and total bilirubin (3.57%). CONCLUSION The combination of TACE and tislelizumab, with or without targeted therapy, demonstrated promising efficacy and safety in unresectable HCC, especially in immunotherapy-naive patients, warranting further prospective validation studies.
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