Abstract | THE AIM OF THE STUDY: 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.
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Authors | V T Ivashkin, V V Gorbakov, B N Lytsar', A P Vasil'ev |
Journal | Terapevticheskii arkhiv
(Ter Arkh)
Vol. 69
Issue 8
Pg. 31-7
( 1997)
ISSN: 0040-3660 [Print] Russia (Federation) |
Vernacular Title | Terapevticheskaia éffektivnost' interferona-al'fa-2a (roferona-A) pri khronicheskikh gepatitakh C. |
PMID | 9381387
(Publication Type: Clinical Trial, Comparative Study, Journal Article)
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Chemical References |
- Antiviral Agents
- Interferon alpha-2
- Interferon-alpha
- Recombinant Proteins
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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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