Advances in treatment have led to improved survival of patients with cancer, but have also increased morbidity and mortality due to cancer treatment side effects. Cardiotoxicity is one the most frequent side effect which may lead to premature morbidity and death among cancer survivors. The most concerning cardiovascular complications of cancer therapy is myocardial dysfunction, leading to heart failure, and fatal arrhythmias, especially those induced by QT-prolonging drugs. PROMETEY (PROspective Multidisciplinary obsErvational Trial of cardiotoxicity in patiEnts undergoing anticancer therapy) - is Russian multicenter observational study assessing cardiotoxicity and its clinical, biochemical and genetic factors in patients on cancer therapy. The objectives of the study are: * to reveal prevalence of cardiotoxic effects of cancer therapy in routine clinical practice in Russian Federation, * to assess contribution of these effects to mortality of patients on cancer therapy, * to evaluate clinical and economic consequences of cardiotoxicity in patients with cancer, * to develop an individualized model of cardiotoxicity risk factors based on clinical and laboratory parameters. Patients: 400 cancer patients with toxic cardiomyopathy and 100 patients with idiopathic or family dilated cardiomyopathy. Study duration: 60 months. All patients will undergo complex examination after signing informed consent form(ICF): physical exam, echocardiography with speckle tracking analysis, ambulatory 48-hours ECG monitoring, biochemistry, analysis of biomarkers of myocardial injury, fibrosis and inflammation. Primary endpoint: all-cause mortality, heart transplantation, cardioverter-defibrillator implantation, hospitalization with heart failure decompensation. Secondary endpoints: * thromboembolism, * fatal/ nonfatal myocardial infarction, stroke, * sudden cardiac death, * surgical therapy of heart failure or arrhythmias, * cardiovascular death, * all-cause mortality, * heart transplantation, * cardioverter-defibrillator implantation.
Study Type
OBSERVATIONAL
Enrollment
500
Transthoracic echocardiography with speckle tracking analysis.
Ambulatory 48-hour electrocardiography monitoring.
Analysis of blood samples for biochemistry, biomarkers of myocardial damage, fibrosis and inflammation.
Moscow State University of Medicine and Dentistry, Department of Hospital Therapy №1
Moscow, Moscow Oblast, Russia
RECRUITINGAll-cause mortality
Death of patient from all causes.
Time frame: During all observational period (60 months)
Heart transplantation
Heart transplantation associated with heart failure or toxic cardiomyopathy decompensation.
Time frame: During all observational period (60 months).
Cardioverter-defibrillator implantation
Implantation of cardioverter-defibrillator associated with life-threatening ventricular arrhythmias.
Time frame: During all observational period (60 months).
Hospitalization with heart failure decompensation
Hospitalization of patient due to decompensation of heart failure.
Time frame: During all observational period (60 months)
Thromboembolism.
Venous thromboembolism associated with cancer disease.
Time frame: During all observational period (60 months).
Myocardial infarction
Fatal/nonfatal myocardial infarction.
Time frame: During all observational period (60 months).
Stroke
Stroke
Time frame: During all observational period (60 months).
Sudden cardiac death
Sudden cardiac death associated with fatal arrhythmias.
Time frame: During all observational period (60 months).
Surgical therapy of heart failure or arrhythmias
Surgical therapy of heart failure or arrhythmias.
Time frame: During all observational period (60 months).
Cardiovascular death
Death of patient associated with cardiovascular disease.
Time frame: During all observational period (60 months).
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