Published online Sep 27, 2024. doi: 10.4240/wjgs.v16.i9.2829
Revised: July 11, 2024
Accepted: August 1, 2024
Published online: September 27, 2024
Processing time: 209 Days and 5.9 Hours
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.
To investigate effectiveness and safety of TACE with tislelizumab ± targeted therapy for unresectable HCC in real-world setting.
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.
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%).
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.
Core Tip: Combining transarterial chemoembolization with tislelizumab ± targeted therapy shows promise for treating unresectable hepatocellular carcinoma (HCC). In this real-world study of 56 cases, median progression-free survival (PFS) and overall survival were 14.0 and 28 months, respectively. Notably, individuals with prior immunotherapy had shorter PFS. The approach demonstrated high objective response rate and disease control rate, with manageable adverse events. These findings support further investigation and validate the potential of this combination therapy in HCC management, especially in immunotherapy-naive patients.