| Inclusion criteria | Exclusion criteria |
---|---|---|
Acute Cohort | 1. Aged <18 years at time of cancer diagnosis; 2. Diagnosed with a new malignancy; 3. Cancer treatment plan will require therapy with ≥1 dose of an anthracycline chemotherapy 4. Pre-anthracycline; echocardiograms to occur at the recruiting site; 5. Normal cardiac function prior to the initiation of anthracycline therapy (LVEF >55%). | 1. Patients with significant congenital heart defects; 2. Patients who were previously treated with anthracycline chemotherapy or radiation to the chest. |
Survivor Cohort | 1. Aged <18 years at time of cancer diagnosis; 2. Previously diagnosed with cancer and currently in remission; 3. Patients whose prior treatment plan included therapy with ≥1 dose of anthracycline chemotherapy; 4. Patients who completed their final dose of anthracycline ≥3 years ago; 5. Patients who completed their final dose of a chemotherapy agent other than anthracycline ≥1 year ago; 6. Routinely followed at the recruiting site approximately every 12 months. | 1. Prior allogeneic stem cell transplant; 2. Patients with significant congenital heart defects; 3. CMR: general contraindications for a contrast enhanced CMR, and patients who require anaesthesia for MRI (typically <6 years of age) will be excluded. |