JOHN M. KIRKWOOD, M.D.; MARC S. ERNSTOFF, M.D.; CAROL A. DAVIS, R.N., M.S.N.; MICHAEL REISS, M.D.; RODOLFO FERRARESI, M.D.; SETH A. RUDNICK, M.D.
▸ Requests for reprints should be addressed to John M. Kirkwood, M.D.; Section of Medical Oncology, Department of Internal Medicine, Yale University School of Medicine, 333 Cedar Street, P.O. Box 3333; New Haven, CT 06510.
KIRKWOOD JM, ERNSTOFF MS, DAVIS CA, REISS M, FERRARESI R, RUDNICK SA. Comparison of Intramuscular and Intravenous Recombinant Alpha-2 Interferon in Melanoma and Other Cancers. Ann Intern Med. 1985;103:(1):32-36. doi: 10.7326/0003-4819-103-1-32
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Published: Ann Intern Med. 1985;103(1):32-36.
In two phase I-II trials, 33 patients were given recombinant interferon alpha-2 daily at dosages of 3, 10, 30, 50, or 100 MU/d for up to 4 weeks by intramuscular or intravenous routes. Dose-limiting toxicities, including neutropenia, elevated hepatocellular enzyme levels, fatigue, and disturbed mentation, correlated with differing serum pharmacokinetics of interferon in the two trials. In the intramuscular study, dose-limiting toxicity occurred at all dosages greater than 10 MU/d, at a median of 6 to 9 days of treatment. In the intravenous dose-study, limiting toxicity was seen only at dosages of 100 MU/d, at a median of day 8. Twenty-three patients had metastatic melanoma and 4 had objective partial or complete responses at dosages of 10 to 50 MU/d in the first month. Two patients with complete responses are free of tumor after 2.5 years of follow-up. A fifth patient had delayed complete regression, requiring 1 year to achieve maximum response, but remains free of disease at 26 months since entry to the trial. Interferon had antitumor activity against melanoma by both routes tested, at dosages of 10 to 50 MU/d.
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Print ISSN: 0003-4819 | Online ISSN: 1539-3704
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