Human leucocyte interferon-alpha in the treatment of chronic hepatitis C

Dig Liver Dis. 2001 May;33(4):347-52. doi: 10.1016/s1590-8658(01)80090-6.

Abstract

Aim: To assess the efficacy of different schedules of human leucocyte interferon alpha in chronic hepatitis C.

Patients and methods: A total of 213 naive patients with chronic hepatitis C were treated with 4 different schedules of human leucocyte interferon alpha. Sustained response was defined as persistently normal alanine amino transferase values with negative serum hepatitis C virus-RNA up to 12 months after therapy withdrawal.

Results: Rates of sustained response were 16% with 3 MU tiw for 6 months, 33% with 6 MU tiw for 5 months after a priming dose of 9 MU tiw for a month, 32% with 3 MU tiw for 12 months and 20% with 3 MU daily for 6 months. The major factors affecting the response rate were age and the hepatitis C virus genotype, as a sustained response was significantly higher in patients under 45 years and infected by hepatitis C virus types other than hepatitis C virus-1. Treatment was well tolerated and side-effects and drop-out events were similar to those described with other types of alpha-interferons.

Conclusions: Human leucocyte interferon alpha appears to be equivalent to recombinant interferon-alpha in the treatment of chronic hepatitis C.

MeSH terms

  • Alanine Transaminase / blood
  • Antiviral Agents / administration & dosage
  • Antiviral Agents / therapeutic use*
  • Drug Administration Schedule
  • Female
  • Hepatitis C, Chronic / drug therapy*
  • Humans
  • Interferon-alpha / administration & dosage
  • Interferon-alpha / therapeutic use*
  • Male
  • Middle Aged
  • Multivariate Analysis
  • RNA, Viral / blood
  • Time Factors

Substances

  • Antiviral Agents
  • Interferon-alpha
  • RNA, Viral
  • Alanine Transaminase