Abstract | BACKGROUND AND AIMS: The intramuscular use of beta interferon has been tested in the treatment of chronic hepatitis C, but it did not prove effective when the schedule was 3 million units three times a week for six months. Since the lack of effectiveness of this treatment might be due to the low bioavailability of beta interferon when administered intramuscularly, we tested a higher dosage of the drug: 6 million units three times a week for twelve months. PATIENTS AND METHODS: Ninety-two patients were randomized to receive, intramuscularly, either 3 or 6 million units of natural human fibroblast beta interferon three times a week for 12 months. RESULTS: The short-term biochemical response was significantly more frequent in the group of patients who received the higher dosage of beta interferon: 21% vs 4.5% (p < 0.05). Nevertheless, a sustained biochemical response was obtained in only one patient (2%), who received the higher dosage of beta interferon. CONCLUSIONS: Since the better short-term response rate was obtained with the higher dosage of beta interferon, a further increase in the dosage might improve the short-term and, possibly, the long-term response to treatment. However, due to the high cost of beta interferon, this high-dose schedule would probably not be cost-effective in the treatment of chronic hepatitis C.
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Authors | E Fesce, A Airoldi, L Mondazzi, G Maggi, G Gubertini, G Bernasconi, P Del Poggio, F Bozzetti, G Idéo |
Journal | Italian journal of gastroenterology and hepatology
(Ital J Gastroenterol Hepatol)
Vol. 30
Issue 2
Pg. 185-8
(Apr 1998)
ISSN: 1125-8055 [Print] Italy |
PMID | 9675656
(Publication Type: Clinical Trial, Journal Article, Randomized Controlled Trial)
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Chemical References |
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Topics |
- Adult
- Drug Administration Schedule
- Female
- Follow-Up Studies
- Hepatitis C, Chronic
(drug therapy)
- Humans
- Injections, Intramuscular
- Interferon-beta
(administration & dosage)
- Male
- Middle Aged
- Reference Values
- Treatment Outcome
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