HER-2/neu is an independent prognostic factor in type I endometrial adenocarcinoma

Arch Gynecol Obstet. 2014 Dec;290(6):1231-7. doi: 10.1007/s00404-014-3333-2. Epub 2014 Jul 15.

Abstract

Purpose: To define the prognostic significance of HER-2/neu and PTEN expression in patients with endometrioid (type I) endometrial cancer.

Methods: Seventy-seven patients with endometrioid endometrial carcinoma were included in the study, in a period between 1996 and 2009. Patients with coexisting malignancy and those having incomplete immunohistochemical data or clinical follow-up were excluded. Histological staging was defined according to the revised FIGO staging (2009). Clinico-pathologic and immunohistochemical characteristics were correlated in a multivariate Cox regression analysis with overall survival (OS), cancer-related survival (CRS) and disease-free survival (DFS).

Results: Mean age of the patients was 62.7 years. The median follow-up was 67 months (9-124 months). HER-2/neu expression was detected in 18.2 % (n = 14), and PTEN expression in 72.7 % (n = 56) of our patients. Multivariate Cox regression analysis showed that patient's age, FIGO staging and HER-2/neu expression were independent prognostic factors for OS, CRS and DFS. PTEN expression did not significantly affect survival outcomes of the present study.

Conclusions: HER-2/neu but not PTEN expression is an independent prognostic factor for type I endometrial carcinoma.

MeSH terms

  • Adenocarcinoma / pathology
  • Carcinoma, Endometrioid / mortality
  • Carcinoma, Endometrioid / pathology
  • Disease-Free Survival
  • Endometrial Neoplasms / mortality
  • Endometrial Neoplasms / pathology*
  • Female
  • Follow-Up Studies
  • Greece
  • Humans
  • Multivariate Analysis
  • Neoplasm Grading
  • Neoplasm Staging
  • PTEN Phosphohydrolase / metabolism*
  • Prognosis
  • Proportional Hazards Models
  • Receptor, ErbB-2 / metabolism*
  • Survival Rate
  • Tissue Array Analysis
  • Treatment Outcome

Substances

  • ERBB2 protein, human
  • Receptor, ErbB-2
  • PTEN Phosphohydrolase
  • PTEN protein, human