Why the study?
Does myocardial FDG uptake on interim PET/CT detect early Adriamycin-induced cardiotoxicity in patients receiving Adriamycin therapy?
Does myocardial FDG uptake on interim PET/CT detect early Adriamycin-induced cardiotoxicity in patients receiving Adriamycin therapy?
Increased myocardial FDG uptake on interim PET/CT may serve as an early, noninvasive imaging biomarker for Adriamycin-induced cardiotoxicity before clinical deterioration occurs.
May signal early Adriamycin cardiotoxicity on PET/CT; hypothesis-generating and requires prospective validation before clinical adoption.
Cumulative cardiotoxicity is a well-established adverse effect of Adriamycin therapy. Although dose dependent, cardiotoxicity has been recently reported to occur even at lower doses than usually proposed. Conventional imaging detection and/or clinical manifestation of the deterioration in cardiac function occur late in the process; thus, it is desirable to have noninvasive markers to detect toxicity at an early stage. Several biochemical markers including troponin and atrial natriuretic peptide were explored for this purpose. The present case depicts that a significant increase in myocardial FDG uptake on posttherapy PET/CT can be a potential imaging biomarker of Adriamycin-induced cardiotoxicity.
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Gorla et al. (2016) studied this question.
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