Clinicopathologic and prognostic characteristics of triple-negative breast cancer

Onkologie. 2008 Nov;31(11):610-4. doi: 10.1159/000162288. Epub 2008 Oct 27.

Abstract

Background: Triple-negative breast cancer (estrogen receptor (ER)-, progesterone receptor (PR)-, and HER2-negative) is a rare subtype with a poor prognosis. However, the clinicopathologic and prognostic characteristics of triple-negative breast cancer remain undetermined.

Materials and methods: Immunohistochemical staining was adopted to examine the expressions of ER, PR, p53, C-erbB-2 (HER2), vascular endothelial growth factor (VEGF), and epidermal growth factor receptor (EGFR) protein in 116 samples of paraffin-embedded breast cancer tissues.

Results: 22 triple-negative breast cancers were found among 116 informative cases (19%). The triple-negative phenotype significantly correlates with tumor size, histological grade, lymph node status, p53, and EGFR (p < 0.05), and not significantly with age, menopausal status, and VEGF protein. After a median follow-up period of 96 months (range: 32-123 months), 12 triple-negative breast cancer patients and 20 patients with non-triple-negative phenotype had distant relapse (p < 0.05). Survival analysis showed that triple-negative phenotype was inversely associated with overall survival (p < 0.05) but not significantly with disease-free survival (p = 0.2877). Multivariate Cox model analysis showed that tumor size, lymph node status, histological grade, and triple-negative phenotype provided independent significant predictive power.

Conclusion: Triple-negative breast cancer phenotype has specific clinical and biological characteristics. Patients with triple-negative breast cancer have a poorer prognosis. So far, there is no conclusive effective treatment, which necessitates further studies.

MeSH terms

  • Adult
  • Age Distribution
  • Aged
  • Asian People / statistics & numerical data*
  • Breast Neoplasms / classification
  • Breast Neoplasms / ethnology*
  • Breast Neoplasms / metabolism*
  • China / ethnology
  • Female
  • Humans
  • Prevalence
  • Receptor, ErbB-2 / metabolism*
  • Receptors, Estrogen / metabolism*
  • Receptors, Progesterone / metabolism*
  • Retrospective Studies
  • Risk Assessment / methods*
  • Risk Factors

Substances

  • Receptors, Estrogen
  • Receptors, Progesterone
  • Receptor, ErbB-2