Sequencing of systemic treatment for hepatocellular carcinoma: Second line competitors

World J Gastroenterol. 2020 Apr 28;26(16):1888-1900. doi: 10.3748/wjg.v26.i16.1888.

Abstract

During the last decades, further knowledge of hepatocellular carcinoma (HCC) molecular mechanisms has led to development of effective systemic treatments including tyrosine kinase inhibitors (TKIs) and immunotherapy. In this review, we describe first and second line systemic treatment options for advanced HCC. Several trials have evaluated new drugs for the treatment of HCC patients: In first line, lenvatinib resulted non-inferior to sorafenib and it can be used as alternative, even in the lack of evidence for sequential treatment options in second line after lenvatinib. Recently, atezolizumab plus bevacizumab have shown superiority over sorafenib in first-line. Sorafenib-regorafenib sequential administration in selected patients has opened a new paradigm of treatment in advanced HCC with a life expectancy exceeding two years. Other TKIs for second line treatment include cabozantinib and ramucirumab (specifically for patients with Alpha-fetoprotein values ≥ 400 ng/mL). The combination of TKIs with immunotherapy may represent a big step forward for these patients in the near future.

Keywords: Advanced; Future; Hepatocellular carcinoma; Options; Sequencing; Systemic.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents, Immunological / administration & dosage*
  • Antineoplastic Combined Chemotherapy Protocols / administration & dosage*
  • Carcinoma, Hepatocellular / drug therapy*
  • Carcinoma, Hepatocellular / immunology
  • Carcinoma, Hepatocellular / mortality
  • Carcinoma, Hepatocellular / pathology
  • Humans
  • Liver Neoplasms / drug therapy*
  • Liver Neoplasms / immunology
  • Liver Neoplasms / mortality
  • Liver Neoplasms / pathology
  • Molecular Targeted Therapy / methods
  • Neoplasm Staging
  • Prognosis
  • Progression-Free Survival
  • Protein Kinase Inhibitors / administration & dosage*
  • Randomized Controlled Trials as Topic

Substances

  • Antineoplastic Agents, Immunological
  • Protein Kinase Inhibitors