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Clinical Trials/NCT05781672
NCT05781672
Terminated
Not Applicable

Longitudinal Analysis of Myocardial Function by Speckle Tracking Echocardiography and Prediction of Delayed Toxic Cardiomyopathy Associated With Anthracycline Therapy in Children

University Hospital, Montpellier1 site in 1 country134 target enrollmentMarch 16, 2023

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cardiotoxicity
Sponsor
University Hospital, Montpellier
Enrollment
134
Locations
1
Primary Endpoint
Left Ventricle Global Longitudinal 2D strain (LVGLS) expressed in percentage and obtained from cardiac ultrasound cineloop of 2D 4,3 and 2 apical views analyzed by the Tomtec STE Software.
Status
Terminated
Last Updated
last year

Overview

Brief Summary

Longitudinal analysis of myocardial function using "Speckle Tracking Echocardiography" STE analysis and prediction of delayed toxic induced cardiomyopathy in young patients who received anthracycline therapy in childhood.

Detailed Description

Anthracycline therapy may have short-, medium- or long-term cardiac toxicity that impacts patient's life. The main recognized risk factors for delayed cardiotoxicity are cumulative anthracycline dose, female gender, association with mediastinal radiotherapy and young age at administration. Prediction of delayed cardiotoxicity in children population is still challenging. The "Speckle Tracking Echocardiography" (STE) method, an innovative echocardiographic technique, analyses the myocardial displacement of natural acoustic markers via a software. The objective of the study is to analyze, in young patients who received anthracycline therapy in childhood, 5-years after their inclusion in the "Speckle Anthra" study and first STE results, the evolution of myocardial function using STE method.

Registry
clinicaltrials.gov
Start Date
March 16, 2023
End Date
January 7, 2025
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Patients who were treated with anthracyclines for malignant disease between the ages of 0 and 18
  • Patient aged 11 to 27 years
  • Included in the "SpeckleAnthra" Study (NCT02893787)
  • Discontinued chemotherapy for more than 6 years
  • Patient in remission of malignant disease
  • Enrolled in a social security plan
  • Written informed consent from at least one legal representative for the minor patient/ Written informed consent for patients of legal age

Exclusion Criteria

  • Onset of active malignancy or recurrence of malignancy after the "Speckle Anthra" study that required resumption of chemotherapy or mediastinal radiotherapy.
  • Chronic cardiac, pulmonary or muscular pathology of etiology other than secondary to anthracycline therapy
  • For adult patients: subject under guardianship or curators
  • CONTROL GROUP
  • Inclusion Criteria:
  • Control patient included in the "Speckle Control" study (NCT02056925)
  • Had a cardiological consultation with echocardiography performed for a banal reason (heart murmur test, cardiological symptoms) and whose result was normal
  • No chronic disease or long-term drug treatment
  • Exclusion Criteria:
  • Refusal to participate in the study by the patient and/or parents or legal guardian after receipt of the study's information and non-objection note.

Outcomes

Primary Outcomes

Left Ventricle Global Longitudinal 2D strain (LVGLS) expressed in percentage and obtained from cardiac ultrasound cineloop of 2D 4,3 and 2 apical views analyzed by the Tomtec STE Software.

Time Frame: 5 years

To compare the evolution at 5 years ("Anthra2" study timeframe) of LVGLS obtained by STE analysis on patients treated with anthracyclines in childhood and previously included in first "Speckle Anthra" study, with the normal evolution of this parameter with age in healthy matched volunteers.

Secondary Outcomes

  • Left Ventricle Ejection fraction (LVEF) by Simpson method (%)(The day of inclusion)
  • Left ventricular myocardial dysfunction defined by LVEF < 55%(5 years)
  • Death secondary to toxic cardiomyopathy(5 years)

Study Sites (1)

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