A phase-I clinical study of low-dose oral interferon-alpha

J Immunother Emphasis Tumor Immunol. 1993 Jul;14(1):51-5.

Abstract

Twenty-five patients with systemic malignancies or cutaneous disorders were treated with low dosages (1-16 IU/kg/day) of oral interferon-alpha in a phase-I study. There were no grade-3 or -4 toxicities. No patients achieved a partial or complete response. One patient with renal cell carcinoma had prolonged disease stabilization lasting for 22 months. No significant changes in lymphocyte subsets including T4/T8 ratio, or serum immunoglobulins were observed. Subjective improvement in general well-being was reported by three patients. Low dosages of interferon-alpha administered orally do not appear to have any significant immunomodulatory or antitumor activity.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase I
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Administration, Oral
  • Adult
  • Aged
  • CD4-CD8 Ratio
  • Drug Tolerance
  • Female
  • Humans
  • Immunoglobulins / blood
  • Immunotherapy
  • Interferon alpha-2
  • Interferon-alpha / administration & dosage*
  • Interferon-alpha / adverse effects
  • Lymphocyte Subsets / immunology
  • Male
  • Middle Aged
  • Neoplasms / immunology
  • Neoplasms / therapy*
  • Recombinant Proteins
  • Skin Diseases / immunology
  • Skin Diseases / therapy*

Substances

  • Immunoglobulins
  • Interferon alpha-2
  • Interferon-alpha
  • Recombinant Proteins