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[The therapeutic efficacy of interferon-alfa-2a (Roferon-A) in chronic hepatitis C].

AbstractTHE AIM OF THE STUDY:
Evaluation of 6-month treatment with roferon-A of patients with chronic hepatitis C (CHC) and comparison of the treatment regimens.
MATERIAL AND METHODS:
79 CHC patients received roferon-A for 3 months in a dose 6,000,000 IU 3 time a week. In case of the response to treatment was continued for the next 3 months (3,000,000 IU 3 times a week). Clinical-laboratory findings, results, of EIA and liver biopsy histology were examined.
RESULTS:
Primary remission was achieved in 71.8% of cases. 36.9% of patients developed recurrences including 14.1% recurrence arising in the course of therapy. Stable remission was obtained in 32.4% of patients. 28.2% patients were non-responders. Side effects were mild, discontinuation of the treatment was necessary only in 7% of cases.
CONCLUSION:
Roferon-A administration in a dose 6,000,000 IU for 24 weeks is optimal both as related to cost and efficacy of the treatment.
AuthorsV T Ivashkin, V V Gorbakov, B N Lytsar', A P Vasil'ev
JournalTerapevticheskii arkhiv (Ter Arkh) Vol. 69 Issue 8 Pg. 31-7 ( 1997) ISSN: 0040-3660 [Print] Russia (Federation)
Vernacular TitleTerapevticheskaia éffektivnost' interferona-al'fa-2a (roferona-A) pri khronicheskikh gepatitakh C.
PMID9381387 (Publication Type: Clinical Trial, Comparative Study, Journal Article)
Chemical References
  • Antiviral Agents
  • Interferon alpha-2
  • Interferon-alpha
  • Recombinant Proteins
Topics
  • Adolescent
  • Adult
  • Aged
  • Analysis of Variance
  • Antiviral Agents (adverse effects, therapeutic use)
  • Chi-Square Distribution
  • Chronic Disease
  • Dose-Response Relationship, Drug
  • Hepatitis C (diagnosis, therapy)
  • Humans
  • Interferon alpha-2
  • Interferon-alpha (adverse effects, therapeutic use)
  • Middle Aged
  • Patient Selection
  • Prognosis
  • Recombinant Proteins
  • Remission Induction
  • Time Factors

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