The importance of EGFR as a biomarker in molecular apocrine breast cancer

Xiaozhen Liu1, Changyun Feng2, Junjun Liu1

  • 1Department of Breast Cancer Pathology and Research Laboratory, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center of Cancer, Key Laboratory of Cancer Prevention and Therapy, Tianjin, Tianjin's Clinical Research Center for Cancer, Key Laboratory of Breast Cancer Prevention and Therapy, Tianjin Medical University, Ministry of Education, Ti Yuan Bei, Hexi District, Tianjin 300060, China.

Human Pathology
|February 8, 2018
PubMed

Insights

Molecular apocrine breast cancer (MABC) has a poor prognosis. Epidermal growth factor receptor (EGFR) expression is linked to worse outcomes and may serve as a therapeutic target in MABC.

Area of Science:

  • Oncology
  • Molecular Biology
  • Cancer Research

Background:

  • Molecular apocrine breast cancer (MABC) is an aggressive subtype requiring novel therapeutic strategies.
  • Epidermal growth factor receptor (EGFR) is implicated in tumor cell behavior and is a target in other cancers.

Purpose of the Study:

  • To investigate the clinical significance and prognostic value of EGFR expression in MABC.
  • To explore potential therapeutic targets for MABC.

Main Methods:

  • Analysis of 400 invasive breast cancer patients (200 MABC, 200 non-MABC).
  • Immunohistochemistry and immunofluorescence to assess expression of AR, EGFR, HER2, and Ki67.
  • Correlation analysis between EGFR expression and clinical parameters/outcomes.

Main Results:

  • EGFR expression was detected in 53% of cases (173 MABC, 39 non-MABC).
  • EGFR expression correlated positively with androgen receptor (AR) expression, advanced tumor stage, and high Ki67 in MABC.
  • Patients with EGFR expression exhibited poorer clinical outcomes compared to those without.

Conclusions:

  • EGFR is a significant prognostic biomarker in MABC, associated with worse outcomes.
  • Co-expression of EGFR and HER2 may predict even poorer outcomes in MABC.
  • Targeting AR and EGFR may be crucial for guiding MABC treatment decisions.