Phase II Trial of a Combination of Interferon-βser and Interferon-γ in Patients with Advanced Malignant Melanoma

J. H. Schiller, B. Storer, G. Bittner, J. K V Willson, E. C. Borden

Research output: Contribution to journalArticle

29 Scopus citations

Abstract

Based upon the in vitro synergistic activity of interferon-β (IFN-β) and interferon-γ (IFN-γ) observed in melanoma cells, we initiated a Phase II trial using the combination to determine the clinical antitumor efficacy in patients with advanced disease. Fifteen patients with metastatic malignant melanoma were given 2,000 μg of recombinant IFN-γ (rIFN-γ) (Biogen) intravenously (i.v.) over 10 min, followed by a 10 min i.v. injection of 30 million units of recombinant IFN-β (rIFN-βser) (Triton) 3 × /week. Six patients had skin, soft tissue, nodal, or subcutaneous metastases, 6 had visceral disease only, and 3 had both. Seven patients had received prior treatment, including chemotherapy (6), radiotherapy (3), and/or immunotherapy (3). Side effects included typical IFN constitutional symptoms such as anorexia, fatigue, nausea, and myalgias, but were not dose limiting. The mean drop in the white blood cell count (WBC) following 1 month of therapy, compared to baseline, was 3.3 × l03/mm2 (p = 0.002); the mean increase in SGOT was 24.1 U/l (p < 0.001). One patient had a dose reduction for Grade III anorexia and fatigue which did not resolve with repeated treatment. One patient with liver metastases had radiographical and clinical stabilization of his disease for 1 year. No responses were seen. The median time to progression was 6 weeks. Two patients' tumors were evaluable in the human tumor colony forming assay (HTCFA) and were markedly sensitive to the antiproliferative effects of IFN combinations. Both patients, however, failed to respond clinically. We conclude that the combination of IFN-γ and IFN-βser, when administered by this dose and schedule, was well tolerated but not effective in metastatic malignant melanoma.

Original languageEnglish (US)
Pages (from-to)581-589
Number of pages9
JournalJournal of Interferon Research
Volume8
Issue number5
DOIs
StatePublished - Oct 1988

ASJC Scopus subject areas

  • Immunology
  • Virology

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