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Symptomatic Heart Failure in Acute Leukemia Patients Treated With Anthracyclines

OBJECTIVES: The purpose of this study was to investigate the occurrence and develop a risk score for heart failure (HF) in acute leukemia. BACKGROUND: Knowledge is scarce regarding the incidence and risk factors of symptomatic HF in patients with acute leukemia. METHODS: Baseline clinical and echoca...

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Detalles Bibliográficos
Autores principales: Kang, Yu, Assuncao, Bruna Leal, Denduluri, Srinivas, McCurdy, Shannon, Luger, Selina, Lefebvre, Bénédicte, Carver, Joseph, Scherrer-Crosbie, Marielle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7472996/
https://www.ncbi.nlm.nih.gov/pubmed/32905430
http://dx.doi.org/10.1016/j.jaccao.2019.10.008
Descripción
Sumario:OBJECTIVES: The purpose of this study was to investigate the occurrence and develop a risk score for heart failure (HF) in acute leukemia. BACKGROUND: Knowledge is scarce regarding the incidence and risk factors of symptomatic HF in patients with acute leukemia. METHODS: Baseline clinical and echocardiographic parameters, including indices of cardiac function (left ventricular ejection fraction and myocardial strain [global longitudinal strain; GLS]), were obtained in 450 patients with acute leukemia treated with anthracyclines, before chemotherapy initiation. Potential risk factors for HF were evaluated using Fine and Gray’s regression analysis, and from this, a 21-point risk score was generated. RESULTS: Forty patients (8.9%) developed HF. The HF risk score included a baseline GLS >−15% (indicative of greater impairment) (6 points), baseline left ventricular ejection fraction <50%, pre-existing cardiovascular disease, acute myeloid leukemia (4 points each), cumulative anthracycline dose ≥250 mg/m(2) (2 points), and age >60 years (1 point). Patients were stratified into low (score 0 to 6), moderate (score 7 to 13), and high risk (score 14 to 21). The estimated 1-year cumulative incidence of HF for low-, moderate-, and high-risk groups was 1.0%, 13.6%, and 35.0%, respectively (p < 0.001). The HF risk score was also predictive of all-cause mortality (p < 0.001). After adjustment for age and leukemia type, however, only GLS was significantly associated with all-cause mortality (hazard ratio: 1.73; 95% confidence interval: 1.30 to 2.31; p < 0.001). CONCLUSIONS: We developed a baseline risk score to determine risk of HF in patients with acute leukemia. Additional studies are needed to determine the external validity of these findings.