A pilot study to evaluate the effects of C1 esterase inhibitor on the toxicity of high-dose interleukin 2

Br J Cancer. 1994 Mar;69(3):596-8. doi: 10.1038/bjc.1994.109.

Abstract

In a pilot study six patients received 4 days' treatment with interleukin 2 (IL-2) [cumulative dose (CD) 264 +/- 26 x 10(6) IU m-2] and C1 esterase inhibitor (C1-INH) (loading dose 2,000 U, followed by 500-1,000 U twice daily). Toxicity was compared with that in patients given 4 days' treatment with standard (CD 66 +/- 12 x 10(6) IU m-2) or escalating-dose (CD 99 +/- 8 x 10(6) IU m-2) IL-2. IL-2-induced hypotension was equivalent and complement activation was less after IL-2 + C1-INH (C3a = 10.5 +/- 3.2 nmol l-1) than following standard (14.1 +/- 8.4 nmol l-1) or escalating-dose (18.3 +/- 2.9 nmol l-1) IL-2. This study demonstrates that C1-INH administration during IL-2 treatment is safe and warrants further study to evaluate its ability to ameliorate IL-2-induced toxicity.

Publication types

  • Comparative Study

MeSH terms

  • Adult
  • Blood Pressure / drug effects
  • Carcinoma, Renal Cell / blood
  • Carcinoma, Renal Cell / physiopathology
  • Carcinoma, Renal Cell / therapy*
  • Complement C1 Inactivator Proteins / administration & dosage
  • Complement C1 Inactivator Proteins / therapeutic use*
  • Complement C3a / metabolism
  • Female
  • Humans
  • Infusions, Intravenous
  • Interleukin-2 / toxicity*
  • Kidney Neoplasms / blood
  • Kidney Neoplasms / physiopathology
  • Kidney Neoplasms / therapy*
  • Male
  • Melanoma / blood
  • Melanoma / physiopathology
  • Melanoma / therapy*
  • Middle Aged
  • Pilot Projects

Substances

  • Complement C1 Inactivator Proteins
  • Interleukin-2
  • Complement C3a