Her2/neu expression predicts the response to antiaromatase neoadjuvant therapy in primary breast cancer: subgroup analysis from celecoxib antiaromatase neoadjuvant trial

Clin Cancer Res. 2004 Jul 15;10(14):4639-44. doi: 10.1158/1078-0432.CCR-04-0057.

Abstract

Purpose: Many studies suggest that Her2/neu play an important role in neoadjuvant endocrine therapy. This study aimed to determine whether the level of Her2/neu expression in advanced breast cancer changes after antiaromatase neoadjuvant treatment, as well as to identify the relationship between Her2/neu expression and response to this kind of therapy.

Experimental design: Thirty-six postmenopausal patients with hormonal receptor-positive primary breast cancer were included in a study of three monthly cycles of neoadjuvant endocrine therapy with either Aromasin (25 mg daily) or Femara (2.5 mg daily). Immunohistochemistry (IHC) and fluorescence in situ hybridization (FISH) for Her2/neu were conducted both on pretreatment biopsies and surgical tumors.

Results: Using IHC, 5 of 36 (13.9%) of the patients had a Her2/neu overexpression after treatment, as compared with 16 of 36 (44.4%) before. Meanwhile, there was no change in 21 (58.3%) patients, and through FISH, there was a change from amplification to no amplification in 15 (41.7%) patients. The response rate to the treatment was 75% for Her2/neu (+) tumors and 35% for Her2/neu (-) tumors (P = 0.017) while FISH was performed. The response rate was also significantly affected by the decrease in Her2/neu status after the treatment, with 73% of the tumors showing decreased Her2/neu expression and with 38% of the tumors showing no change of Her2/neu expression (P = 0.037).

Conclusions: Using both IHC and FISH, advanced breast cancers show statistical evidence of decreasing incidence of Her2/neu expression after antiaromatase neoadjuvant treatment. Our data also suggest that Her2/neu expression and its change during the treatment might be predictive markers for this kind of therapy.

Publication types

  • Clinical Trial
  • Comparative Study
  • Controlled Clinical Trial

MeSH terms

  • Aged
  • Aged, 80 and over
  • Androstadienes / therapeutic use
  • Antineoplastic Agents / therapeutic use
  • Aromatase Inhibitors / therapeutic use*
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / therapy*
  • Celecoxib
  • Cyclooxygenase Inhibitors / therapeutic use
  • Female
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization, Fluorescence
  • Letrozole
  • Middle Aged
  • Neoadjuvant Therapy
  • Nitriles / therapeutic use
  • Prognosis
  • Pyrazoles / therapeutic use
  • Receptor, ErbB-2 / analysis
  • Receptor, ErbB-2 / genetics*
  • Sulfonamides / therapeutic use
  • Treatment Outcome
  • Triazoles / therapeutic use

Substances

  • Androstadienes
  • Antineoplastic Agents
  • Aromatase Inhibitors
  • Cyclooxygenase Inhibitors
  • Nitriles
  • Pyrazoles
  • Sulfonamides
  • Triazoles
  • Letrozole
  • Receptor, ErbB-2
  • Celecoxib
  • exemestane