The aromatase inhibitors in early breast cancer: who, when, and why?

Med J Aust. 2005 Jul 4;183(1):24-7. doi: 10.5694/j.1326-5377.2005.tb06882.x.

Abstract

The aromatase inhibitors deplete oestrogen by inhibiting aromatase, the enzyme that synthesises oestrogen from androgens. They are effective as therapies for breast cancer only in postmenopausal women whose tumours express oestrogen or progesterone receptors. As adjuvant therapy, tamoxifen and the aromatase inhibitors have similar efficacy in the first 5 years of treatment. Aromatase inhibitors can be used as an alternative to tamoxifen in women with symptomatic intolerance or a contraindication to tamoxifen. Early data suggest that switching to an aromatase inhibitor after 2-5 years of tamoxifen therapy is beneficial in women with high-risk disease. Aromatase inhibitors are associated with more hot flushes than placebo, but with fewer hot flushes, less endometrial toxicity and venous thromboembolism, and more arthralgia, myalgia and bone fracture than tamoxifen.

Publication types

  • Review

MeSH terms

  • Anastrozole
  • Aromatase Inhibitors / therapeutic use*
  • Breast Neoplasms / drug therapy*
  • Drug Evaluation
  • Drug Therapy, Combination
  • Female
  • Humans
  • Letrozole
  • Nitriles / therapeutic use
  • Patient Selection*
  • Selective Estrogen Receptor Modulators / therapeutic use
  • Survival Analysis
  • Tamoxifen / therapeutic use
  • Treatment Outcome
  • Triazoles / therapeutic use

Substances

  • Aromatase Inhibitors
  • Nitriles
  • Selective Estrogen Receptor Modulators
  • Triazoles
  • Tamoxifen
  • Anastrozole
  • Letrozole