Alterations in Left Atrial Strain in Breast Cancer Patients Immediately Post Anthracycline Exposure

Heart Lung Circ. 2024 May;33(5):684-692. doi: 10.1016/j.hlc.2023.06.864. Epub 2023 Oct 6.

Abstract

Aims: With improved diagnosis and treatments, a greater percentage of breast cancer patients are achieving long-term survival. Consequently, long-term cardiotoxicity secondary to chemotherapy has become more prevalent, warranting improved cardiac surveillance. We evaluated changes in left atrial (LA) strain in breast cancer patients immediately post anthracycline (AC) therapy to assess its utility as a marker of diastolic dysfunction.

Methods: This was a prospective cohort study of 128 consecutive human epidermal growth factor receptor 2 (HER2)-negative breast cancer patients who underwent transthoracic echocardiography prior to and immediately post AC treatment. Traditional left ventricular (LV) systolic and diastolic parameters and LA volumes were evaluated; additionally, LV global longitudinal strain (LV GLS) and LA phasic strain were measured.

Results: All patients had normal LV ejection fraction (>53%) post AC, though LV GLS was significantly reduced. Peak E and é velocities were reduced post AC, with no change in LA volumes. LA reservoir strain (LASRES 34.8% vs 31.5%, p<0.001) and conduit strain (LASCD 17.2% vs 14.4%, p<0.001) were significantly lower post AC and correlated modestly with LV diastolic parameters. Reduction in LA strain post AC was evident even in patients with preserved LV systolic and diastolic function. More patients demonstrated alteration in diastolic function (≥15% reduction in LASRES from baseline) (32%) compared to alteration in systolic function (≥15% reduction in LV GLS) (23%).

Conclusions: LA strain is a promising marker of early diastolic dysfunction. We demonstrate its potential utility in surveillance of breast cancer patients treated with AC.

Keywords: Anthracycline; Breast cancer; Cardiotoxicity; Left atrial strain.

MeSH terms

  • Adult
  • Aged
  • Anthracyclines* / adverse effects
  • Atrial Function, Left / drug effects
  • Atrial Function, Left / physiology
  • Breast Neoplasms* / drug therapy
  • Cardiotoxicity / etiology
  • Echocardiography* / methods
  • Female
  • Follow-Up Studies
  • Heart Atria* / diagnostic imaging
  • Heart Atria* / drug effects
  • Heart Atria* / physiopathology
  • Humans
  • Middle Aged
  • Prospective Studies
  • Stroke Volume / drug effects
  • Stroke Volume / physiology
  • Ventricular Function, Left / drug effects
  • Ventricular Function, Left / physiology

Substances

  • Anthracyclines