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Approaches to Identify Early Biomarkers and Pathogenesis of Anthracycline Cardiotoxicity

Integrated Basis and Translational Approaches to Identify Early Biomarkers and Pathogenesis of Anthracycline Cardiotoxicity

Status
Withdrawn
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04036045
Enrollment
0
Registered
2019-07-29
Start date
2018-11-12
Completion date
2025-03-31
Last updated
2025-10-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Childhood Cancer

Keywords

Anthracycline induced cardiotoxicity

Brief summary

Early microRNAs (miRs) and Cardiac Magnetic Resonance (CMR)-derived strain analysis and detection of genes contributing to Anthracycline-Induced Cardiotoxicity (AIC) sensitivity and resistance will identify pediatric cancer patients most and least likely to develop AIC.

Detailed description

Plan is to enroll 110 children and adults (≥9 years old) newly diagnosed at CCMC and Nationwide Children's Hospital (55 per institution) who will receive anthracyclines as part of their chemotherapy regimen. The duration of study participation will be approximately a year. Patients will have a total of four study visits: Baseline 1 week after patient's anthracycline cumulative dose hits between 60 and 100 mg/m2 After the patient has completed maximal therapy One year after completion of anthracycline treatments Study tasks for all four visits will be: Collection of clinical data Blood draw for micro RNA and Biomarkers Cardiac MRI Echocardiogram One time blood draw for genetics

Interventions

OTHERCardiac MRI

Patients will have a cardiac MRI at four time points during the study

OTHEREchocardiogram

Patients will have an echocardiogram at four time points during the study

OTHERBlood Draw

Patients will have blood drawn at four time points to analyze micro RNAs and Biomarkers before, during and after anthracycline treatment. Patients will also have one blood draw for future genetic sequencing.

Sponsors

Nationwide Children's Hospital
CollaboratorOTHER
Connecticut Children's Medical Center
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
9 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Age (≥ 9years old) * Newly diagnosed with a malignancy that will receive ACs as part of their chemotherapy. * Parental/caregiver consent and subject assent to enrollment.

Exclusion criteria

* Subject has contraindications to CMR.\* * Subject requiring sedation for CMR * Subject too large to be safely accommodated by CMR * Pregnancy tests are done routinely prior to chemotherapy, if test is positive the patient will be excluded * Subject's serum creatinine above guidelines for adequate renal function. See table below: Age (years) Male Female 6-10 1.0 mg/dL 1.0 mg/dL 10-13 1.2 mg/dL 1.2 mg/dL 13-16 1.5 mg/dL 1.4 mg/dL \>16 1.7 mg/dL 1.4 mg/dL

Design outcomes

Primary

MeasureTime frameDescription
CMRFrom Baseline to one year after anthracycline therapy1\. Increased myocardial T2 relaxation time in the myocardium compared to baseline as measured by T2 mapping technique

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026