Biomarkers of residual disease after neoadjuvant therapy for breast cancer

Nat Rev Clin Oncol. 2016 Aug;13(8):487-503. doi: 10.1038/nrclinonc.2016.1. Epub 2016 Feb 9.

Abstract

Nowadays, the decision of which adjuvant treatment should be given to patients with residual breast cancer after neoadjuvant therapy is based on the initial, pretreatment breast cancer molecular subtype and on the estimated residual tumour burden after neoadjuvant therapy. Substantial biological differences exist, however, between treatment-naive breast cancer and the residual tissue that remains after neoadjuvant therapy. In addition, the evaluation of relapse risk in patients is subject to a lack of uniformity in pathological qualification and quantification of remnant breast cancer following neoadjuvant treatment. In this Review, we present the recent recommendations for standardized evaluation of response to neoadjuvant therapy in patients with breast cancer, followed by a comprehensive overview of the pathobiological features of the residual disease after neoadjuvant therapy, which could serve as prognostic biomarkers or guide the choice of targeted adjuvant approaches. These biomarker candidates are at different stages of development, but some already have demonstrated superior prognostic value compared with biomarkers derived from pretreatment breast-cancer characteristics. The evidence presented herein indicates that further research on the biology of breast cancer that persists after neoadjuvant therapy is necessary to improve the management of this disease.

Publication types

  • Review

MeSH terms

  • Biomarkers, Tumor / metabolism*
  • Breast Neoplasms / genetics
  • Breast Neoplasms / pathology
  • Breast Neoplasms / therapy*
  • Female
  • Genetic Markers / genetics
  • Humans
  • Ki-67 Antigen / metabolism
  • Mutation / genetics
  • Neoadjuvant Therapy
  • Neoplasm Grading
  • Neoplasm, Residual / diagnosis*
  • Neoplasm, Residual / genetics
  • Neoplasm, Residual / pathology
  • Proteome / genetics
  • Receptor, ErbB-2 / metabolism
  • Treatment Outcome
  • Tumor Burden
  • Tumor Microenvironment / immunology

Substances

  • Biomarkers, Tumor
  • Genetic Markers
  • Ki-67 Antigen
  • Proteome
  • Receptor, ErbB-2