Cardiotoxicity of trastuzumab emtansine (T-DM1): a single-center experience

J Int Med Res. 2021 Dec;49(12):3000605211053755. doi: 10.1177/03000605211053755.

Abstract

Objective: New anti-cancer drugs promise to increased survival benefits and reduce adverse events. Trastuzumab emtansine (T-DM1) is a novel anti-human epidermal growth factor receptor 2 agent that has shown minimal cardiotoxicity in clinical trials. However, data on real-life outcomes are required.

Methods: A retrospective review of our center's medical records was performed, including female patients aged ≥18 years with a diagnosis of metastatic breast cancer who were treated with T-DM1. Descriptive statistics were used to investigate clinical features that could increase the risk of cardiotoxicity. Cardiotoxicity was determined by comparing pre and post-T-DM1 echocardiogram results and was defined as a decrease in the left ventricular ejection fraction (LVEF) >10% to below 55%.

Results: Data from 41 female patients with a mean age of 52 ± 11.5 years were evaluated. A significant LVEF decrease (from 59% to 33%) was observed in one patient during T-DM1 treatment. Further investigation showed that this decrease was due to underlying coronary artery disease, and LVEF recovered to the baseline value after coronary revascularization.

Conclusion: T-DM1 seems to be safe in terms of cardiotoxicity. Real-life data with a larger sample size are still needed to confirm the cardiac safety of T-DM1.

Keywords: Breast cancer; cardiotoxicity; echocardiogram; left ventricular ejection fraction; metastatic breast cancer; trastuzumab emtansine.

MeSH terms

  • Ado-Trastuzumab Emtansine
  • Adolescent
  • Adult
  • Breast Neoplasms* / drug therapy
  • Cardiotoxicity* / etiology
  • Female
  • Humans
  • Middle Aged
  • Receptor, ErbB-2
  • Retrospective Studies
  • Stroke Volume
  • Ventricular Function, Left

Substances

  • Receptor, ErbB-2
  • Ado-Trastuzumab Emtansine