Tolerability of Molecular-targeted Agents for Hepatocellular Carcinoma Treatment in Haemophiliacs

Anticancer Res. 2021 May;41(5):2569-2573. doi: 10.21873/anticanres.15035.

Abstract

Background: Hepatocellular carcinoma (HCC) is considered a leading cause of death in patients with haemophilia. Recent advances in the treatment of unresectable HCC with molecular-targeted agents (MTAs) have led to better clinical outcomes. However, the tolerability of MTAs by haemophilic patients with HCC remains unclear.

Aim: This study aimed to compare the tolerability of MTAs in such patients.

Patients and methods: From January 2011 to October 2020, five haemophilic patients with HCC were treated with MTAs. Adverse events were assessed in comparison with 265 non-haemophilic patients with HCC.

Results: The prevalence of hand-foot skin reaction was not higher in the haemophiliacs than in the non-haemophiliacs, whereas the rate of haemorrhagic events was higher in the haemophiliacs (6.0% versus 40.0%, p=0.037).

Conclusion: Haemophiliacs tolerate long-term MTA use, without the occurrence of life-threatening complications. However, careful observation and prevention are needed for MTA-related gastrointestinal bleeding in haemophiliacs.

Keywords: Haemophilia; hepatocellular carcinoma; molecular-targeted agents.

MeSH terms

  • Aged
  • Carcinoma, Hepatocellular / complications
  • Carcinoma, Hepatocellular / drug therapy*
  • Carcinoma, Hepatocellular / genetics
  • Carcinoma, Hepatocellular / pathology
  • Drug Tolerance / physiology
  • Female
  • Gastrointestinal Tract / drug effects
  • Gastrointestinal Tract / pathology
  • Hemophilia A / complications
  • Hemophilia A / drug therapy*
  • Hemophilia A / genetics
  • Hemophilia A / pathology
  • Hemorrhage / complications
  • Hemorrhage / drug therapy
  • Hemorrhage / genetics
  • Hemorrhage / pathology
  • Humans
  • Liver Neoplasms / complications
  • Liver Neoplasms / drug therapy*
  • Liver Neoplasms / genetics
  • Liver Neoplasms / pathology
  • Male
  • Middle Aged
  • Molecular Targeted Therapy*