Immuno-Oncology in Hepatocellular Carcinoma: 2017 Update

Masatoshi Kudo1

  • 1Department of Gastroenterology and Hepatology, Kindai University Faculty of Medicine, Osaka-Sayama, Japan.

Oncology
|December 20, 2017
PubMed

Insights

Immune checkpoint inhibitors, including antibodies targeting programmed cell death 1 (PD-1), programmed cell death-ligand 1 (PD-L1), and cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4), show promise for hepatocellular carcinoma (HCC). Combination therapies are being explored to enhance anti-cancer immunity.

Area of Science:

  • Immunology
  • Oncology
  • Hepatology

Background:

  • Hepatocellular carcinoma (HCC) remains a significant health challenge, with limited effective treatment options.
  • Immune checkpoint inhibitors targeting PD-1, PD-L1, and CTLA-4 are emerging as a promising therapeutic strategy.
  • Current research focuses on optimizing the use of these inhibitors as monotherapy or in combination for HCC treatment.

Purpose of the Study:

  • To evaluate the efficacy of immune checkpoint inhibitors in hepatocellular carcinoma.
  • To explore combination therapies involving anti-PD-L1 and anti-CTLA-4 antibodies.
  • To investigate novel therapeutic combinations for HCC, including molecular targeted agents.

Main Methods:

  • Clinical trials assessing PD-1, PD-L1, and CTLA-4 antibodies in HCC patients.
  • Presentation of results from combination therapy with durvalumab (anti-PD-L1) and tremelimumab (anti-CTLA-4) at ASCO 2017.
  • Nonclinical studies evaluating the combination of pembrolizumab and lenvatinib.

Main Results:

  • Encouraging response rates of 25% overall and 40% in uninfected patients with durvalumab and tremelimumab combination therapy.
  • Transcatheter arterial chemoembolization and radiofrequency ablation can enhance tumor immunogenicity.
  • Pembrolizumab and lenvatinib combination therapy demonstrated inhibition of immunosuppressive factors and activation of anti-cancer immunity.

Conclusions:

  • Combination immunotherapy, such as anti-PD-L1 and anti-CTLA-4, shows potential in treating HCC.
  • Local therapies can be combined with immune checkpoint inhibitors to improve outcomes.
  • Further research is needed to identify optimal molecular targeted agents for combination with immune checkpoint inhibitors in HCC.

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