Drug Safety

, Volume 17, Issue 1, pp 1–7

Mitochondrial Injury

Lessons from the Fialuridine Trial
  • Pieter Honkoop
  • Hans R. Scholte
  • Robert A. de Man
  • Solko W. Schalm
Leading Article

DOI: 10.2165/00002018-199717010-00001

Cite this article as:
Honkoop, P., Scholte, H.R., de Man, R.A. et al. Drug-Safety (1997) 17: 1. doi:10.2165/00002018-199717010-00001

Summary

Fialuridine is an antiviral agent with potent activity against hepatitis B virus replication in vitro and in vivo. In a phase II study, 7 of 15 patients experienced severe toxicity due to the drug after 9 to 13 weeks of treatment. Adverse effects included nausea, vomiting and painful paraesthesia; subsequently, hepatic failure, pancreatitis, neuropathy, myopathy and lactic acidosis developed, probably due to multisystem mitochondrial toxicity.

Possible mechanisms of fialuridine toxicity include mitochondrial injury and pyruvate oxidation inhibition. While other nucleoside analogues have shown evidence of inducing mitochondrial injury (zidovudine, didanosine, zalcitabine), others to date have not (lamivudine, famciclovir). Specific recommendations for future study of existing and new nucleoside analogues include testing for toxicity after prolonged incubation, specific investigations to measure mitochondrial function, toxicological tests and well designed clinical trials with appropriate testing to monitor for any adverse effects on mitochondrial integrity and function.

Copyright information

© Adis International Limited 1997

Authors and Affiliations

  • Pieter Honkoop
    • 1
  • Hans R. Scholte
    • 2
  • Robert A. de Man
    • 1
  • Solko W. Schalm
    • 1
  1. 1.Department of Internal Medicine II (Section Hepatology)Erasmus University HospitalRotterdamThe Netherlands
  2. 2.Department of BiochemistryErasmus University HospitalRotterdamThe Netherlands
  3. 3.Department of Internal Medicine II (Ca 326)Erasmus University HospitalRotterdamThe Netherlands