Four-Dimensional Echocardiographic Evaluation of Left Ventricular Systolic Functions in Patients with Chronic Myeloid Leukaemia Receiving Tyrosine Kinase Inhibitors.
Adult
Aged
Antineoplastic Agents
/ adverse effects
Cardiotoxicity
Cross-Sectional Studies
Dasatinib
/ adverse effects
Early Diagnosis
Echocardiography, Four-Dimensional
Female
Humans
Imatinib Mesylate
/ adverse effects
Leukemia, Myelogenous, Chronic, BCR-ABL Positive
/ diagnosis
Male
Middle Aged
Predictive Value of Tests
Protein Kinase Inhibitors
/ adverse effects
Protein-Tyrosine Kinases
/ antagonists & inhibitors
Pyrimidines
/ adverse effects
Retrospective Studies
Risk Assessment
Systole
Time Factors
Treatment Outcome
Ventricular Dysfunction, Left
/ chemically induced
Ventricular Function, Left
/ drug effects
Chronic myeloid leukaemia
Strain
Systolic functions
Tyrosine kinase inhibitor
Journal
Cardiovascular toxicology
ISSN: 1559-0259
Titre abrégé: Cardiovasc Toxicol
Pays: United States
ID NLM: 101135818
Informations de publication
Date de publication:
03 2021
03 2021
Historique:
received:
02
06
2020
accepted:
10
10
2020
pubmed:
18
10
2020
medline:
15
12
2021
entrez:
17
10
2020
Statut:
ppublish
Résumé
Tyrosine kinase inhibitors (TKIs) are established treatment for haematological malignancies. However, cardiac adverse effects, including the reduction in left ventricular ejection fraction and symptomatic heart failure remain clinical problems. The purpose of this study was to evaluate the left ventricular systolic functions in patients with chronic myeloid leukaemia receiving TKIs. A cross-sectional and observational study was conducted of 37 patients with chronic myeloid leukaemia receiving dasatinib or nilotinib after imatinib failure. Left ventricular systolic functions were evaluated using four-dimensional speckle tracking echocardiography derived global longitudinal (GLS), circumferential (GCS), radial (GRS), and area (GAS) strain indices. Mean ejection fraction, stroke volume, cardiac output and left ventricular mass index were similar between control and patient groups and within normal limits. GLS (- 16.7% vs - 20.8%, p < 0.001), GCS (- 13.0% vs - 15.6%, p = 0.002), and GAS (- 26.2% vs - 31.0, p < 0.001) values were significantly higher in the patient population than those of the controls. Dasatinib and nilotinib groups did not show differences regarding strain indices. In multivariate regression analysis, only the usage of dasatinib or nilotinib was found to be an independent risk factor for diminished GAS (β = 4.406, p = 0.016), GLS (β = 3.797, p = 0.001), and GCS (β = 2.404, p = 0.040). Although imatinib, nilotinib, and dasatinib seem to be clinically safe in terms of cardiac function, monitoring of systolic functions using strain imaging, and long-term observation of patients may provide early detection of the possible cardiac toxicity.
Identifiants
pubmed: 33068232
doi: 10.1007/s12012-020-09613-2
pii: 10.1007/s12012-020-09613-2
doi:
Substances chimiques
Antineoplastic Agents
0
Protein Kinase Inhibitors
0
Pyrimidines
0
Imatinib Mesylate
8A1O1M485B
Protein-Tyrosine Kinases
EC 2.7.10.1
nilotinib
F41401512X
Dasatinib
RBZ1571X5H
Types de publication
Journal Article
Observational Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
216-223Références
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