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May 7, 2026Liver Cancer0 citationsOpen Access

Addition of Intra-arterial Therapy to Immunotherapy Improves Outcomes in Unresectable Hepatocellular Carcinoma: Taiwan Multicenter Cohort Study

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TLTeng-Yu LeePLPei-Chang LeeYSYing-Chun Shen

Key Points

  • This study evaluates the impact of intra-arterial therapy addition to immunotherapy on survival outcomes in unresectable hepatocellular carcinoma.
  • Identified patients with unresectable HCC receiving immunotherapy from TLCA Research Group database.
  • Excluded patients with BCLC stage A or D disease and those with prior liver transplantation.
  • Eligible patients received either IAT or immunotherapy alone with 1:3 propensity score matching.
  • Analyzed overall survival using adjusted hazard ratios in a time-dependent model.
  • IAT group had higher objective response rate of 46.7% compared to 26.3% in the control group (P<0.001).
  • IAT contributed to longer duration of response (median 19.0 weeks in IAT vs 11.0 weeks in control; P=0.009).
  • IAT was associated with improved overall survival (adjusted HR 0.53; P<0.001).
  • Five-year OS was 28.7% in IAT group versus 16.4% in control (P=0.007).
  • Subgroup analyses confirmed the benefit of IAT on overall survival.

Abstract

Introduction: Evidence supporting the combination of immunotherapy with intra-arterial therapy (IAT) for unresectable hepatocellular carcinoma (HCC) remains limited. This study aimed to evaluate whether the addition of IAT to first-line immunotherapy improves survival outcomes. Methods: Using the Taiwan Liver Cancer Association (TLCA) Research Group database, we identified patients with unresectable HCC who initiated first-line immunotherapy between May 2017 and January 2024. Patients with Barcelona Clinic Liver Cancer (BCLC) stage A or D disease, prior liver transplantation, or follow-up of 1 (aHR 1.58, 95% CI: 1.11-2.27; P=0.012), tumor burden beyond the up-to-7 criteria (aHR 1.67, 95% CI: 1.02-2.74; P=0.043), and portal vein invasion (aHR 1.67; 95% CI: 1.19-2.35; P=0.003). Five-year OS was higher in the IAT group than in the control group (28.7% 95% CI: 17.8-46.2 vs. 16.4% 95% CI: 10.7-25.2; P=0.007). Landmark and subgroup analyses consistently supported the OS benefit of IAT. Conclusion: In unresectable HCC, the addition of IAT to first-line immunotherapy improves response rates, prolongs the duration of response, and enhances OS.

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Cite This Study

Lee et al. (2026) studied this question.

synapsesocial.com/papers/69fbefd5164b5133a91a3e94https://doi.org/10.1159/000552375
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