Immunotherapy for Advanced Hepatocellular Carcinoma-a Large Tertiary Center Experience

J Gastrointest Surg. 2023 Oct;27(10):2126-2134. doi: 10.1007/s11605-023-05783-w. Epub 2023 Jul 18.

Abstract

Introduction: Combination of immune-checkpoint inhibitor (ICI) and vascular endothelial growth factor (VEGF) antagonist has become the first line systemic treatment for advanced hepatocellular carcinoma (HCC). However, two-thirds of patients do not respond to ICI-based treatments and biomarkers for response remain elusive.

Methods: Patients with advanced HCC who received Atezolizumab/Bevacizumab combination or Nivolumab during 2016-2022 were identified in our Liver Cancer Database. Retrospective review of their clinical data was performed to investigate parameters that could be predictive of immunotherapy response.

Results: 96 patients received Atezolizumab/Bevacizumab (n=60) or Nivolumab (n=36). Median age at diagnosis was 67.1 years. 70 patients had received treatment and 26 patients were treatment naïve before starting immunotherapy. Mean pre-treatment AFP was 9780.7 (±32035) ng/mL. Confirmed objective response (complete or partial) was seen in 29% of the population (n=27). Disease remained stable in 12% (n=11) and progressed in 60% (n=56). On univariate analysis, pre-treatment AFP>400 ng/mL was associated with objective response (OR=4.5, 95% CI:1.7-11.9, p=0.0015), while white race (OR=0.35, 95% CI:0.13-0.92, p=0.030) and prior radiotherapy (OR=0.14, 95% CI:0.01-1.1, p=0.033) or systemic therapy with TKIs (OR=0.25, 95% CI:0.08-0.81, p=0.017) were associated with poor response. On multivariate analysis only AFP>400 ng/mL remained associated with response (OR=3.7, 95% CI:1.3-10.5, p=0.014). Overall survival (OS) at one and three years was 86% and 43% in responders, and 45% and 29% in non-responders, respectively.

Conclusion: In our institutional experience, treatment naivety and pre-treatment AFP>400 ng/mL were associated with objective response. Prospective studies aimed at identifying factors associated with response to immunotherapy will aide patient selection.

Keywords: advanced hepatocellular carcinoma; alpha fetoprotein; immune checkpoint inhibitors; immunotherapy; tyrosine kinase inhibitors; vascular endothelial growth factor antagonist.

MeSH terms

  • Aged
  • Bevacizumab / therapeutic use
  • Carcinoma, Hepatocellular* / pathology
  • Carcinoma, Hepatocellular* / therapy
  • Humans
  • Immunotherapy
  • Liver Neoplasms* / pathology
  • Nivolumab / therapeutic use
  • Prospective Studies
  • Treatment Outcome
  • Vascular Endothelial Growth Factor A / therapeutic use
  • alpha-Fetoproteins / metabolism

Substances

  • Bevacizumab
  • alpha-Fetoproteins
  • Vascular Endothelial Growth Factor A
  • Nivolumab