Effect of raloxifene on IGF-I and IGFBP-3 in postmenopausal women with breast cancer

Br J Cancer. 2001 Dec 14;85(12):1838-41. doi: 10.1054/bjoc.2001.2191.

Abstract

The effect on the IGF system of 60 mg and 600 mg daily of raloxifene administered for 2 weeks prior to surgery was investigated in 37 postmenopausal women with breast cancer. Raloxifene significantly decreased insulin-like growth factor (IGF-I) as compared to placebo (P < 0.05) with no dose-response relationship. No significant change was observed in IGFBP-3, while the IGF-I/IGFBP-3 molar ratio was decreased by treatment, with a statistically significant effect only for the higher dose. Given that high plasma levels of IGF-I have been suggested as a risk factor for breast cancer, these findings provide further support for the potential activity of raloxifene in breast cancer prevention.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase II
  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antineoplastic Agents, Hormonal / administration & dosage
  • Antineoplastic Agents, Hormonal / pharmacology*
  • Antineoplastic Agents, Hormonal / therapeutic use
  • Breast Neoplasms / blood*
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / surgery
  • Chemotherapy, Adjuvant
  • Depression, Chemical
  • Dose-Response Relationship, Drug
  • Female
  • Humans
  • Insulin-Like Growth Factor Binding Protein 3 / blood*
  • Insulin-Like Growth Factor I / analysis*
  • Mastectomy
  • Middle Aged
  • Neoplasm Proteins / blood*
  • Postmenopause
  • Premedication
  • Raloxifene Hydrochloride / administration & dosage
  • Raloxifene Hydrochloride / pharmacology*
  • Raloxifene Hydrochloride / therapeutic use*
  • Selective Estrogen Receptor Modulators / administration & dosage
  • Selective Estrogen Receptor Modulators / pharmacology*
  • Selective Estrogen Receptor Modulators / therapeutic use

Substances

  • Antineoplastic Agents, Hormonal
  • Insulin-Like Growth Factor Binding Protein 3
  • Neoplasm Proteins
  • Selective Estrogen Receptor Modulators
  • Raloxifene Hydrochloride
  • Insulin-Like Growth Factor I