Comparison of Her-2, EGFR and cyclin D1 in primary breast cancer and paired metastatic lymph nodes: an immunohistochemical and chromogenic in situ hybridization study

J Korean Med Sci. 2008 Dec;23(6):1053-61. doi: 10.3346/jkms.2008.23.6.1053. Epub 2008 Dec 24.

Abstract

The significant advance in the development of molecular-targeting drugs has made an evaluation of Her-2, EGFR, and cyclin D1 an important clinical issue in breast cancer patients. This study compared the Her-2, EGFR, and cyclin D1 status of primary tumors as well as their matching lymph node metastases using immunohistochemistry (IHC) and chromogenic in situ hybridization (CISH) in 73 breast cancer patients. Her-2, EGFR, and cyclin D1 protein showed a concordance between the primary lesion and the metastatic regional lymph nodes in 82%, 90%, and 63%, respectively. CISH also revealed 92%, 93%, and 85% concordance in the gene amplification status of Her-2, EGFR, and cyclin D1, showing a reasonable agreement between primary tumors and metastatic regional lymph nodes. Although a statistically significant agreement was found in Her-2 expression, a relatively high discordance rate (18%) raises a little concern. Our findings suggest that the Her-2 status can be reliably assessed on primary tumor but a possible difference can be found in Her-2, EGFR, and cyclin D1 status between the primary and the metastatic sites and this possibility should be concerned in patients considering molecular targeted therapy or patients with progress of disease.

Keywords: CISH; Cyclin D1; EGFR; Her-2; Immunohistochemistry.

MeSH terms

  • Adult
  • Aged
  • Breast Neoplasms / genetics
  • Breast Neoplasms / metabolism*
  • Breast Neoplasms / pathology
  • Chromogenic Compounds
  • Cyclin D1 / analysis*
  • Cyclin D1 / genetics
  • ErbB Receptors / analysis*
  • ErbB Receptors / genetics
  • Female
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization
  • Lymph Nodes / metabolism*
  • Lymph Nodes / pathology
  • Lymphatic Metastasis
  • Male
  • Middle Aged
  • Neoplasm Recurrence, Local / genetics
  • Neoplasm Recurrence, Local / metabolism
  • Receptor, ErbB-2 / analysis*
  • Receptor, ErbB-2 / genetics
  • Survival Analysis

Substances

  • Chromogenic Compounds
  • Cyclin D1
  • ErbB Receptors
  • Receptor, ErbB-2