Phase II trials of recombinant leukocyte A interferon in disseminated malignant melanoma: results in 96 patients

Cancer Treat Rep. 1986 May;70(5):619-24.

Abstract

Ninety-six patients with advanced malignant melanoma received thrice weekly im recombinant leukocyte A interferon (Roferon-A) in three consecutive phase II trials utilizing doses of 12 X 10(6) U/m2, 50 X 10(6) U/m2, and 50 X 10(6) U/m2 plus cimetidine. The overall response rate was 22%, with median times to disease progression and survival of 3.9 and 11.3 months, respectively. For all study participants, the median times to disease progression and survival were 1.5 and 5 months, respectively. Most regressions occurred within the first month of treatment and were predominantly in soft tissue, although three patients are responding 2-3 years after onset of treatment. The most noteworthy toxic effects included a flu-type illness, anorexia, and fever (38.3-39.4 degrees C). The median weight loss was 2.1 kg on the low-dose regimen and 5.6 kg on the high-dose program. Recombinant leukocyte A interferon in the dosages and schedule that we used has definite but limited efficacy for patients with disseminated malignant melanoma.

Publication types

  • Clinical Trial
  • Comparative Study

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Cimetidine / administration & dosage
  • Clinical Trials as Topic
  • DNA, Recombinant
  • Drug Administration Schedule
  • Drug Evaluation
  • Female
  • Humans
  • Interferon Type I / administration & dosage
  • Interferon Type I / adverse effects
  • Interferon Type I / therapeutic use*
  • Male
  • Melanoma / mortality
  • Melanoma / pathology
  • Melanoma / therapy*
  • Middle Aged
  • Naphthacenes / metabolism
  • Time Factors

Substances

  • DNA, Recombinant
  • Interferon Type I
  • Naphthacenes
  • 7-deoxyadriamycinol aglycone
  • Cimetidine
  • 7-deoxyadriamycin aglycone