Sequencing of endocrine therapy in postmenopausal women with advanced breast cancer

Clin Cancer Res. 2004 Jan 1;10(1 Pt 2):362S-7S. doi: 10.1158/1078-0432.ccr-031200.

Abstract

The introduction of the nonsteroidal aromatase inhibitor (NS-AI) anastrozole as an alternative to tamoxifen for adjuvant therapy of women with resected hormone receptor-positive breast cancer has added a management category into which patients presenting with metastatic disease can be placed. There are now essentially three such categories: (a) tamoxifen sensitive (no prior AI); (b) tamoxifen resistant (no prior AI); and (c) NS-AI resistant (no prior tamoxifen). Well-conducted Phase III trials provide evidence for choosing first-line therapy for advanced disease in categories a and b. In tamoxifen-sensitive patients, one can choose either NS-AI, anastrozole, or letrozole. In tamoxifen-resistant patients, one can choose either of the NS-AIs, the steroidal AI exemestane, or the estrogen receptor down-regulator fulvestrant. The situation is quite different for patients in category c. There are no Phase III trials of agents in patients who have experienced disease progression on a NS-AI. Phase II data are available for exemestane and high-dose estrogens, and retrospective data are available for tamoxifen and fulvestrant. Additional clinical trials are needed to determine an optimal sequencing strategy.

MeSH terms

  • Androstadienes / therapeutic use
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents, Hormonal / pharmacology
  • Antineoplastic Agents, Hormonal / therapeutic use*
  • Breast Neoplasms / drug therapy*
  • Chemotherapy, Adjuvant
  • Clinical Trials as Topic
  • Disease Progression
  • Female
  • Humans
  • Neoplasm Metastasis
  • Neoplasms, Hormone-Dependent / metabolism
  • Postmenopause
  • Receptors, Estrogen / metabolism
  • Tamoxifen / therapeutic use

Substances

  • Androstadienes
  • Antineoplastic Agents
  • Antineoplastic Agents, Hormonal
  • Receptors, Estrogen
  • Tamoxifen
  • exemestane