RecruitingNot ApplicableNCT05703126

Clinical and Diagnostic Significance of Endothelial Dysfunction and Myocardial Contractility in Patients With AML

Clinical and Diagnostic Significance of Endothelial Dysfunction and Myocardial Contractility in Patients With Acute Myeloid Leukemia


Sponsor

Samara State Medical University

Enrollment

100 participants

Start Date

Dec 1, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Acute myeloid leukemia (AML) is a clonal neoplastic disease of the hematopoietic tissue associated with a mutation in the precursor cell of hematopoiesis, which results in a differentiation block and uncontrolled proliferation of immature myeloid cells. Anthracycline antibiotics have been an integral part of the treatment of acute myeloid leukemia since the 1970s. However, the clinical usefulness of anthracyclines is limited primarily by the high incidence of cardiotoxicity. According to the European Society of Cardiology guidelines for cardio-oncology, cardiovascular toxicity is defined as any impairment of cardiac function associated with anticancer treatment, as the term encompasses both a wide range of possible clinical manifestations and an etiological relationship with various treatments, including chemotherapy, radiation therapy, immunotherapy and treatment with targeted drugs. Cardiovascular toxicity can be acute, subacute or delayed, manifesting many years after chemotherapy or radiation therapy, involving a number of cardiac structures, which can lead to the development of heart failure, coronary heart disease, valvular heart disease, arrhythmias, including cardiac conduction disorders and diseases of the pericardium. Anthracycline-induced cardiotoxicity is the negative effect of anthracyclines on normal cardiac activity due to their toxic effects on the heart muscle and the cardiac conduction system. Anthracycline-induced cardiotoxicity manifests as asymptomatic left ventricular dysfunction in 57% of treated patients and restrictive or dilated cardiomyopathy leading to congestive heart failure (CHF) in 16% to 20% of patients. Anthracycline-induced congestive heart failure is often resistant to therapy and has a mortality rate of up to 79%. Thus, there is a need for early detection of cardiovascular dysfunction associated with chemotherapy treatment of acute myeloid leukemia in order to timely prescribe drug therapy. Purpose of the study To optimize the early detection of endothelial dysfunction and left ventricular myocardial contractility in patients with acute myeloid leukemia during chemotherapy treatment based on a comprehensive assessment of instrumental and laboratory research parameters. Expected results Based on a comprehensive analysis using laser Doppler flowmetry, stress echocardiography with the determination of global longitudinal strain of the myocardium, biochemical markers of endothelial damage and cardiac biomarkers, a correlation between violations of the contractility of the left ventricular myocardium and violations of the vasoregulatory function of the vascular endothelium will be revealed, which will allow developing an algorithm for early detection of cardiomyopathy and vascular complications in patients with acute myeloid leukemia during chemotherapy treatment.


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This study is examining how chemotherapy affects the heart in patients with acute myeloid leukemia (AML, a type of blood cancer). Specifically, researchers are measuring heart function and blood vessel health before, during, and after treatment to detect early signs of heart damage. **You may be eligible if...** - You are between 18 and 65 years old - You have been diagnosed with acute myeloid leukemia (AML) - You are about to start chemotherapy that includes a drug class called anthracyclines - Your heart is currently functioning normally (ejection fraction above 50%) - You do not have current signs of heart failure **You may NOT be eligible if...** - You have had a stroke or heart attack in the past - You have diabetes (type 1 or 2) - You have chronic kidney disease - You have unstable angina or significant irregular heartbeats - You have high blood pressure (grade 2-3) - You have HIV, hepatitis B, or hepatitis C - You have alcohol or drug addiction Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DIAGNOSTIC_TESTHistory taking

Careful history taking, including using questionnaires, to identify risk factors for the development of cardiovascular diseases using the SCORE scale.

DIAGNOSTIC_TESTAnthropometry

Anthropometry: measurement of body weight and height. Calculation of body surface area using the Du Bois formula.

DIAGNOSTIC_TESTComplete blood count

Before and after each course of chemotherapy: Complete blood count with counting the number of erythrocytes, leukocytes, leukocyte formula, platelets, erythrocyte sedimentation rate.

DIAGNOSTIC_TESTBiochemical blood test

Before and after each course of chemotherapy: Biochemical blood test with the determination of the amount of total protein, total cholesterol, HDL cholesterol, LDL cholesterol, triglycerides, creatinine, urea, AlAT, AsAT, LDH, glucose, C-reactive protein, troponin T, proBNP.

DIAGNOSTIC_TESTCoagulogram

Before and after each course of chemotherapy: Coagulogram parameters (fibrinogen, APTT, INR).

DIAGNOSTIC_TESTImmunoenzymatic analysis of the level of endothelin-1, asymmetric dimethylarginine

Before the start of the treatment and after each course of chemotherapy: Immunoenzymatic analysis of the level of endothelin-1, asymmetric dimethylarginine.

DIAGNOSTIC_TESTStress echocardiography with the definition of global longitudinal deformation of the myocardium

Before the start of the treatment and after each course of chemotherapy: Stress echocardiography with the definition of global longitudinal deformation of the myocardium.

DIAGNOSTIC_TESTTriplex scanning of neck vessels

Before the start of the treatment and after each course of chemotherapy: Triplex scanning of neck vessels.

DIAGNOSTIC_TESTElectrocardiography

Before and after each course of chemotherapy: Electrocardiography.

DIAGNOSTIC_TESTUltrasound of the abdominal cavity (with calculation of the area of the spleen) and lymph nodes

Before the start of the treatment and after each course of chemotherapy: Ultrasound of the abdominal cavity (with calculation of the area of the spleen) and lymph nodes.

DIAGNOSTIC_TESTCytogenetic examination of the bone marrow to determine genetic abnormalities.

Before the start of the treatment: Cytogenetic examination of the bone marrow to determine genetic abnormalities.

DIAGNOSTIC_TESTCytological examination of bone marrow cells with cytochemical examination

Before the start of the treatment and after each course of chemotherapy: Cytological examination of bone marrow cells with cytochemical examination.

DIAGNOSTIC_TESTImmunophenotypic examination of the bone marrow by flow cytometry

Before the start of the treatment: Immunophenotypic examination of the bone marrow by flow cytometry.

DIAGNOSTIC_TESTDetermination of the presence of a FLT3 mutation using the PCR Method

Before the start of the treatment: Determination of the presence of a FLT3 mutation using the PCR Method.

DIAGNOSTIC_TESTlaser Doppler flowmetry

Before the start of the treatment and after each course of chemotherapy: Examination of microcirculation by laser Doppler flowmetry using the LAKK-OP apparatus (NPP Lazma, Moscow, 2011) with respiratory and occlusion tests.


Locations(1)

Clinics of the Samara Medical University

Samara, Samara Oblast, Russia

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NCT05703126


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