## Abstract ## BACKGROUND The objective of the current study was to examine the risk factors for progression in severity of anthracycline‐induced cardiac dysfunction, thereby providing information that is useful in refining cancer treatment regimes and guiding follow‐up. ## METHODS Serial echoca
Late cardiotoxicity after bolus versus infusion anthracycline therapy for childhood cancers
✍ Scribed by Gupta, Monesha ;Steinherz, Peter G. ;Cheung, Nai-Kong ;Steinherz, Laurel
- Book ID
- 102521200
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 72 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0098-1532
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✦ Synopsis
Abstract
Objective
To compare the long‐term myocardial function of patients who had been treated with infusion anthracycline therapy (administered continuously over >24 hr, IG) versus bolus therapy (administered over <30 min, BG).
Methods
We selected 25 patients (BG) and 19 patients (IG) who had three or more years of disease free survival. We evaluated the echocardiograms for left ventricular shortening fraction (SF) obtained at baseline, within one year after the end of therapy (early follow‐up), and on long‐term follow‐up.
Results
The mean anthracycline dose in the BG was 385 mg/m^2^ and in the IG was 345 mg/m^2^ (P = 0.07). During therapy, one patient in BG and none in IG developed diminished SF. During early follow‐up, five of the 22 patients in BG and one of the 17 patients in IG developed diminished SF (P = 0.2). Of these five patients with diminished SF, three patients in BG and none in IG continued to have abnormally low SF long‐term. At mean of 7 years, five of the 25 patients in BG and two of the 19 in IG had diminished SF on (P = 0.7). Late left ventricular dilatation was seen in 8% in BG and 5% in IG (P = 1.0).
Conclusions
At mean of 7 years after end of therapy, diminished cardiac function was seen in 20% of the patient who had received bolus anthracycline compared to 11% of patients who had received it via infusion. This difference did not prove to be statistically significant. Med Pediatr Oncol 2003;40:343–347. © 2003 Wiley‐Liss, Inc.
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