Review Article
Review of Cardiotoxicity in Pediatric Cancer Patients: During and after Therapy
Table 1
Cancer therapies utilized in pediatric population associated with cardiotoxicity.
| Type of therapy | Dose that places at highest risk | Time of usual presentation | Cardiac manifestations |
| Radiation therapy [5] | >30 gray to heart | Up to decades after treatment has ended | Pericarditis, coronary artery disease, valvular disease, arrythmias |
| Anthracyclines [6, 7] | >300 mg/m2 doxorubicin isotoxic cumulative dose | Acute: during therapy Chronic: months to years posttherapy (longer follow higher the incidence) | Acute-arrythmias, hypotension Chronic-CHF |
| Cyclophosphamide [8, 9] | >150 mg/kg or >1.55 g/m2 given as one dose or per one course | ECG changes: 1–3 days after therapy CHF: up to 2 weeks after therapy | CHF, Myocarditis |
| Cytarabine [8, 9] | High doses | 3–28 days after initiation of therapy | Pericarditis, ventricular, and atrial arrythmias |
| Cisplatin [8, 9] | Usually when receiving with other chemotherapy | Arrythmias/hypotension: acute within hours Vascular toxicities: usually days after infusion but reports 4 and 18 mths post therapy | Arrythmias Vascular toxicities (CVA, AMI) |
| Ifosfamide [9, 10] | Higher doses | 6–23 days after first dose | CHF, arrythmias |
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CHF: Congestive Heart Failure, ECG: Electrocardiogram.
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