Intratumoral depot interleukin-2 therapy inhibits tumor growth in Dunning adenocarcinoma of the prostate implanted subcutaneously in rats

J Cancer Res Clin Oncol. 1997;123(11-12):614-8. doi: 10.1007/s004320050114.

Abstract

The purpose of this study was to determine the effectiveness and toxicity of local continuous immunotherapy of prostatic cancer. A group of 60 young male Copenhagen rats with Dunning adenocarcinoma of the prostate, implanted subcutaneously into both flanks, after proven tumor growth, were treated with either human interleukin-2 (IL-2) depot preparations (n = 30) or albumin (placebo) depot preparations (n = 30) implanted directly into one tumor site. IL-2 depots released IL-2 reliably for more than 24 days. The rat serum was tested during treatment for human IL-2, possibly absorbed from depots, and for rat interferon gamma. IL-2 treatment reduced tumor growth significantly (P < 0.001) compared with albumin-treated sites or untreated contralateral sites. No toxicity was observed during treatment. Neither human IL-2 nor rat interferon gamma was detected in the serum, which indicates an exclusively local IL-2 effect. IL-2 depot preparations reduce tumor growth in Dunning adenocarcinoma of the prostate significantly without toxicity.

MeSH terms

  • Adenocarcinoma / drug therapy*
  • Animals
  • Dose-Response Relationship, Immunologic
  • Humans
  • Injections, Intralesional
  • Interferon-gamma / blood
  • Interleukin-2 / administration & dosage*
  • Interleukin-2 / adverse effects
  • Interleukin-2 / blood
  • Male
  • Neoplasm Transplantation
  • Prostatic Neoplasms / drug therapy*
  • Rats
  • Time Factors

Substances

  • Interleukin-2
  • Interferon-gamma