Combined transarterial chemoembolization and tislelizumab for patients with unresectable hepatocellular carcinoma

医学 肝细胞癌 内科学 免疫疗法 不利影响 实体瘤疗效评价标准 胃肠病学 外科 联合疗法 肿瘤科 进行性疾病 化疗 癌症
作者
Bin-Bin Tan,Ying Fu,Minghua Shao,Hai-Lei Chen,Ping Liu,Fan Chao,Hui Zhang
出处
期刊:World Journal of Gastrointestinal Surgery [Baishideng Publishing Group Co (World Journal of Gastrointestinal Surgery)]
卷期号:16 (9): 2829-2841
标识
DOI:10.4240/wjgs.v16.i9.2829
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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