Similar Efficacy Between Atezolizumab Plus Bevacizumab Versus Hepatic Arterial Infusion Chemotherapy For Unresectable Hepatocellular Carcinoma With Portal Vein Tumor Thrombus: A Retrospective Cohort Study.

AKIFUMI KUWANO; MASAYOSHI YADA; KOSUKE TANAKA; YUTA KOGA; SHIGEHIRO NAGASAWA; AKIHIDE MASUMOTO; KENTA MOTOMURA

Background/Aim: The landscape of treatments for hepatocellular carcinoma (HCC), including immune checkpoint inhibitors, has expanded significantly. However, unresectable HCC patients with portal vein tumor thrombus (PVTT) continue to face a poor prognosis. This investigation examined the survival outcomes and determinants influencing survival rates in advanced HCC patients with PVTT undergoing treatment with atezolizumab plus bevacizumab (ATZ BEV) or hepatic arterial infusion chemotherapy (HAIC). Patients and Methods: Between December 2003 and June 2023, 48 advanced HCC with PVTT underwent treatment with either ATZ BEV (16 patients) or HAIC (32 patients). Results: The analysis revealed no significant disparities in overall survival (OS) or treatment efficacy between the ATZ BEV and HAIC groups (ATZ BEV: 10.0 months, HAIC: 15.3 months). Treatment with either ATZ BEV or HAIC resulted in minimal alterations in the ALBI score and preserved hepatic function. Independent prognostic factors for OS, identified via multivariate logistic regression, included serum a-fetoprotein levels >400 ng/ml [hazard ratio (HR)=1.94; p=0.001], the existence of more than five tumors (HR=1.55; p=0.043), and the Child-Pugh score (HR=2.53; p=0.002). Conclusion: This investigation revealed no significant variance in OS and response rates between patients receiving ATZ BEV and those treated with HAIC. The survival of advanced HCC patients with PVTT is intricately linked to the preservation of liver function, emphasizing the necessity for additional research to enhance treatment approaches for this patient population.

ATEZOLIZUMAB; BEVACIZUMAB; HEPATIC arterial infusion chemotherapy; HEPATOCELLULAR carcinoma; DRUG efficacy

In Vivo, 2024, Vol 38, Issue 4, p1854

0258-851X

Academic Journal

10.21873/invivo.13639