Cardiovascular Toxicity of Novel HER2-Targeted Therapies in the Treatment of Breast Cancer

Curr Oncol Rep. 2021 Aug 27;23(11):128. doi: 10.1007/s11912-021-01114-x.

Abstract

Purpose of review: HER2-targeted therapies have led to improved clinical outcomes in early and advanced breast cancer (BC). We review the long-term cardiotoxicity of HER2-targeted therapy in early and advanced BC, our current knowledge of cardiotoxicity of novel HER2-targeted therapies, and propose a cardiac monitoring (CM) strategy for this population.

Recent findings: Long-term data from studies with HER2-targeted therapy in the adjuvant setting have failed to demonstrate an increase in cardiotoxicity over time, and rates of cardiotoxicity seen with novel HER2 agents remain low. Despite over a decade of experience with HER2-targeted therapy, CM in clinical practice is inconsistent in patients with early BC and almost non-existent in advanced BC. Long-term follow-up of clinical trials with HER2-targeted agents in early and advanced BC has failed to demonstrate increased rates of cardiotoxicity over time, attesting to the long-term safety of this class of drugs for the majority of patients, although the long-term cardiac safety of newer HER2 agents in the non-clinical trial setting is largely unknown. We propose CM incorporating clinical history, cardiac imaging, and biomarkers.

Keywords: Breast cancer; Cardiac monitoring; Cardiotoxicity; Novel HER2 agents.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / adverse effects*
  • Antineoplastic Agents / therapeutic use
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / pathology
  • Cardiotoxicity / diagnosis
  • Cardiotoxicity / etiology*
  • Clinical Trials as Topic
  • Female
  • Humans
  • Immunoconjugates / adverse effects
  • Immunoconjugates / therapeutic use
  • Molecular Targeted Therapy / adverse effects*
  • Molecular Targeted Therapy / methods
  • Protein Kinase Inhibitors / adverse effects
  • Protein Kinase Inhibitors / therapeutic use
  • Receptor, ErbB-2 / antagonists & inhibitors*
  • Receptor, ErbB-2 / metabolism

Substances

  • Antineoplastic Agents
  • Immunoconjugates
  • Protein Kinase Inhibitors
  • ERBB2 protein, human
  • Receptor, ErbB-2