Is there a correlation between HER2 gene amplification level and response to neoadjuvant treatment with trastuzumab and chemotherapy in HER2-positive breast cancer?

Virchows Arch. 2021 Oct;479(4):853-857. doi: 10.1007/s00428-021-03104-7. Epub 2021 May 1.

Abstract

There are contradictory data regarding the correlation between HER2 amplification level determined by in situ hybridization and evolution after treatment with anti-HER2 therapies. The aim of this study was to correlate quantitative results of FISH (ratio HER2/CEP17 and number of HER2 signals/nucleus) with pathological response achieved after neoadjuvant treatment with trastuzumab and chemotherapy. For this purpose, we analysed 100 consecutive HER2-positive cases of breast carcinoma treated with neoadjuvant therapy. HER2 amplification determined by FISH was found in 92 of the 100 cases studied. pCR was obtained in 58% of the patients whose tumours presented amplification. In contrast, no pCR was obtained in the 8 patients with non-amplified tumours. A significant direct correlation between HER2 high amplification (HER2/CEP17 ratio > 5 or HER2 signals/nucleus > 10) and pCR was found. In conclusion, HER2 amplification levels are clinically relevant because they provide oncologists with valuable information on the possibilities of achieving pCR after neoadjuvant treatment.

Keywords: Breast cancer; FISH; HER2 amplification; Neoadjuvant therapy; Pathological complete response; Trastuzumab.

Publication types

  • Review

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Biomarkers, Pharmacological
  • Breast Neoplasms / drug therapy
  • Breast Neoplasms / genetics*
  • Breast Neoplasms / pathology
  • Female
  • Gene Amplification / genetics
  • Humans
  • In Situ Hybridization, Fluorescence / methods
  • Middle Aged
  • Neoadjuvant Therapy / methods
  • Receptor, ErbB-2 / drug effects
  • Receptor, ErbB-2 / genetics*
  • Trastuzumab / therapeutic use
  • Treatment Outcome

Substances

  • Biomarkers, Pharmacological
  • ERBB2 protein, human
  • Receptor, ErbB-2
  • Trastuzumab