Abstract

Background Cardiotoxicity is the main complication related to cancer therapy. Studies indicate that global longitudinal strain is an early detector of subclinical dysfunction of the left ventricle, preceding the decline in ejection fraction (EF). However, the reproducibility of such methodology has not been tested outside specialized centers. Objectives To assess the frequency of subclinical cardiotoxicity and to compare global longitudinal strain and EF measurements during the clinical course of patients undergoing chemotherapy for breast cancer. Methods This was an [...]

Highlights

  • Most chemotherapy agents have adverse side effects, the most feared, due to its morbidity and mortality, is cardiotoxicity

  • Its main etiological agents are anthracyclines and trastuzumab, both of which are widely used in breast cancer treatment. 1–3

  • The frequency of subclinical cardiotoxicity was high from the first month of anthracycline chemotherapy, unlike the results of myocardial dysfunction analysis based exclusively on ejection fraction (EF)

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Summary

Introduction

Most chemotherapy agents have adverse side effects, the most feared, due to its morbidity and mortality, is cardiotoxicity. Studies indicate that global longitudinal strain is an early detector of subclinical dysfunction of the left ventricle, preceding the decline in ejection fraction (EF). Objectives: To assess the frequency of subclinical cardiotoxicity and to compare global longitudinal strain and EF measurements during the clinical course of patients undergoing chemotherapy for breast cancer. Methods: This was an observational prospective study of 78 adult women who underwent serial echocardiograms (baseline and 1, 3, and 6 months after the beginning of chemotherapy), to evaluate biplane and 3D EF and global longitudinal strain. The frequency of subclinical cardiotoxicity (defined by global longitudinal strain) was 14.9% after 30 days of chemotherapy, 16.7% after 3 months, and 19.7% after 6 months, compared to 4.5%, 3%, and 6.6%, respectively, when clinical cardiotoxicity was determined according to EF.

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