The prevalence and clinical significance of HER2 expression in prostate adenocarcinoma

Ann Diagn Pathol. 2023 Dec:67:152219. doi: 10.1016/j.anndiagpath.2023.152219. Epub 2023 Oct 20.

Abstract

Aims: Abnormalities in HER2 are well-established oncogenic drivers and are approved therapeutic targets in various malignancies. Prior studies evaluating HER2 expression in prostate cancer (PCa) have yielded variable results. Most of these studies used immunohistochemistry scoring systems based on breast cancer data. The goal of this study was to determine the prevalence and clinical significance of HER2 expression using a scoring system that better reflects the HER2 staining pattern observed in PCa.

Methods: We randomly selected similar numbers of localized low risk (AJCC stage I), locally advanced (AJCC stages II & III), and metastatic (AJCC stage IV) PCa patients treated at the DC VA Medical Center between 2000 and 2022. Among them, we included patients who had sufficient PCa tissue samples and clinical information required for this analysis. Two experienced pathologists independently scored HER2 expression (Ventana Pathway anti-HER2) according to a modified gastric cancer HER2 scoring system.

Results: Out of the 231 patients included, 85 % self-identified as Black. 58.9 % of patients expressed HER2 (1+: 35.5 %; 2+: 18.2 %; 3+: 5.2 %). Validity of the results was confirmed using the HercepTest antibody. Higher HER2 expression was associated with a higher Gleason Score/Grade Group and advanced disease.

Conclusions: Our findings support the adverse prognostic impact on HER2 in PCa. We propose the use of a modified scoring system to evaluate HER2 expression in PCa. The observed high prevalence of HER2 expression supports the consideration of novel HER2-targeted therapies addressing even low levels of HER2 expression in future PCa trials.

Keywords: Advanced disease; HER2; Immunohistochemistry; Prostate cancer.

MeSH terms

  • Adenocarcinoma* / pathology
  • Clinical Relevance
  • Humans
  • Male
  • Prevalence
  • Prostate / pathology
  • Prostatic Neoplasms* / pathology
  • Receptor, ErbB-2 / metabolism

Substances

  • Receptor, ErbB-2
  • ERBB2 protein, human