This is an observational study of the occurrence of cardiac toxicity in patients with breast cancer,lymphoma or leukemia receiving chemotherapy including an anthracycline. Patients will be identified at the oncology clinic and will be included in the study if all eligible criteria are met. The study will involve retrospective and prospective evaluations. Safety will be assessed through reporting of serious adverse events (SAEs) related to study procedures.
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Myocardial extracellular volume (ECV)
Timeframe: Change from baseline to 3, 6, 12,and 24 months
Myocardial extracellular volume (ECV)
Timeframe: Change from baseline to prior study entry, 12 and 24 months post study entry.