Key result
Allogeneic stem cell transplant survivors show ~4-point lower LVEF compared to healthy controls.
Why the study?
There is limited knowledge of the long-term effects of allogeneic hematopoietic stem cell transplantation on cardiac function in survivors treated in childhood, adolescence, or early adulthood.
Cross-Sectional (n=159)
Observer-blinded
No
Absolute Event Rate: 55.2% vs 59%
p-value: p=<0.001
Indicates substantial LV systolic dysfunction burden in allo-HSCT survivors; leaves optimal surveillance strategies open for prospective validation.
BACKGROUND: Allogeneic hematopoietic stem cell transplantation (allo-HSCT), a potentially curative therapy for malignant and nonmalignant diseases, is being increasingly used in younger patients. Although allo-HSCT survivors have an established increased risk of cardiovascular disease, there is limited knowledge of the long-term effects on cardiac function in survivors. OBJECTIVES: The purpose of this study was to describe left ventricular (LV) systolic function in long-term allo-HSCT survivors treated in childhood, adolescence, or early adulthood. METHODS: Our cross-sectional cohort study included 104 patients (56% women), age 18 ± 10 years at time allo-HSCT with 17 ± 6 years of follow-up. Echocardiography included 2-dimensional (2D) and 3-dimensional (3D) analyses and speckle tracking imaging. In total, 55 healthy control subjects with a similar age, sex, and body mass index were used for comparison. Left ventricular systolic dysfunction (LVSD) was defined as reduced 2D left ventricular ejection fraction (LVEF) of <52% in men and <54% in women, and/or a reduced global longitudinal strain (GLS) of ≥-17%. Multivariable linear regression was used to determine independent predictors of 2D-LVEF and GLS. RESULTS: Allo-HSCT survivors had significantly reduced LV systolic function compared with control subjects: 2D-LVEF (55.2 ± 5.8% vs. 59.0 ± 2.9%; p < 0.001), 3D LVEF (54.0 ± 5.1% vs. 57.6 ± 2.7%; p < 0.001), and GLS (-17.5 ± 2.2% vs. -19.8 ± 1.4%; p < 0.001). LVSD was found in 44.2%, of whom 28.3% were symptomatic. Clinical factors independently associated with 2D-LVEF and/or GLS included age, anthracyclines, graft versus host disease (GVHD), heart rate, and hypertension. In the 45% of survivors pre-treated with anthracyclines, the effect of anthracyclines on 2D-LVEF and GLS was dose-dependent. CONCLUSIONS: LVSD is common in long-term survivors of allo-HSCT treated in their youth. Pre-HSCT therapies with anthracyclines, age, heart rate, hypertension, and graft versus host disease are associated with measures of LV function.
No takes yet. Share an insight, caveat, or question.
Massey et al. (2020) conducted a cross-sectional in Left Ventricular Systolic Dysfunction in allo-HSCT survivors (n=159). Allogeneic hematopoietic stem cell transplantation (allo-HSCT) vs. Healthy control subjects was evaluated on 2D left ventricular ejection fraction (2D-LVEF) (p=<0.001). Long-term survivors of allogeneic hematopoietic stem cell transplantation had significantly reduced 2D-LVEF (55.2% vs 59.0%) and a 44.2% prevalence of left ventricular systolic dysfunction compared to healthy controls.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: