Relationship between regional left ventricular dysfunction and cancer-therapy-related cardiac dysfunction
Yoshihito Saijo1, Kenya Kusunose2, Yuichiro Okushi1
1Department of Cardiovascular Medicine, Tokushima University Hospital, Tokushima, Japan.
Changes in basal longitudinal strain (LS) can predict cancer-therapy-related cardiac dysfunction (CTRCD) in patients receiving anthracycline chemotherapy. A significant decrease in basal LS before CTRCD development indicates a higher risk.
Area of Science:
- Cardiology
- Oncology
- Medical Imaging
Background:
- Cancer therapies, particularly anthracyclines, can lead to cardiotoxicity.
- Early detection of cancer-therapy-related cardiac dysfunction (CTRCD) is crucial for patient management.
- Echocardiography is a key tool for assessing cardiac function during cancer treatment.
Purpose of the Study:
- To evaluate the association between changes in echocardiographic measures and the risk of CTRCD.
- To determine if regional left ventricular (LV) systolic dysfunction predicts CTRCD development after anthracycline therapy.
Main Methods:
- Retrospective analysis of 87 patients receiving anthracyclines, with echocardiograms at baseline and first follow-up.
- Measurement of global longitudinal strain (GLS) and regional LS (apical, mid, basal) and calculation of percentage changes (Δ).
- Assessment of CTRCD development (LV ejection fraction <53% and >10% decrease from baseline) in 61 patients with further follow-up.
Main Results:
- Significant decreases in LVEF, GLS, and basal-LS were observed at first follow-up compared to baseline.
- 13% of patients developed CTRCD. Worse Δbasal-LS was significantly associated with CTRCD development.
- Kaplan-Meier analysis showed worse event-free survival in patients with a greater decrease in Δbasal-LS.
Conclusions:
- Basal-LS reduction precedes the development of CTRCD in patients undergoing anthracycline chemotherapy.
- Worsening basal-LS is a significant predictor of CTRCD.
- Monitoring basal-LS may aid in the early identification of patients at risk for chemotherapy-induced cardiotoxicity.
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