Key result
Among adult 5-year childhood cancer survivors treated with potentially cardiotoxic therapies, 27% had subclinical cardiac dysfunction (LVSF <30%).
Why the study?
What is the prevalence and what are the determinants of left ventricular dysfunction in adult 5-year survivors of childhood cancer treated with potentially cardiotoxic therapies?
Cohort (n=514)
What is the prevalence and what are the determinants of left ventricular dysfunction in adult 5-year survivors of childhood cancer treated with potentially cardiotoxic therapies?
A high percentage (27%) of young adult childhood cancer survivors have subclinical cardiac dysfunction, which is strongly predicted by anthracycline dose, cardiac irradiation, and younger age at diagnosis.
Answers are grounded in this paper and cite their sources.
May warrant enhanced surveillance in anthracycline- or radiation-exposed survivors; leaves open whether early intervention alters long-term outcomes.
BACKGROUND: Childhood cancer survivors (CCSs) have an increased risk of morbidity and mortality. We evaluated the prevalence and determinants of left ventricular (LV) dysfunction in a large cohort of long-term CCSs treated with different potentially cardiotoxic therapies. METHODS: The study cohort consisted of all adult 5-year CCSs who were treated with potentially cardiotoxic therapies and who visited our late effects outpatient clinic. Echocardiography was performed in patients who had received anthracyclines, cardiac irradiation, high-dose cyclophosphamide, or high-dose ifosfamide. Detailed treatment data were registered. Both multivariate linear and logistic regression analyses were performed. RESULTS: Of 601 eligible CCSs, 525 (87%) had an echocardiogram performed, of which 514 were evaluable for assessment of the LV shortening fraction (LVSF). The median overall LVSF in the whole group of CCSs was 33.1% (range, 13.0%-56.0%). Subclinical cardiac dysfunction (LVSF <30%) was identified in 139 patients (27%). In a multivariate linear regression model, LVSF was reduced with younger age at diagnosis, higher cumulative anthracycline dose, and radiation to the thorax. High-dose cyclophosphamide and ifosfamide were not associated with a reduction of LVSF. Vincristine sulfate was associated with a nonsignificant decrease of cardiac function (P = .07). Epirubicin hydrochloride was as cardiotoxic as doxorubicin when corrected for tumor efficacy, and daunorubicin hydrochloride seemed less cardiotoxic. CONCLUSIONS: A high percentage (27%) of young adult CCSs have an abnormal cardiac function. The strongest predictors of subclinical cardiac dysfunction are anthracycline dose, cardiac irradiation, and younger age at diagnosis. There is a suggestion that daunorubicin is less cardiotoxic than other anthracyclines.
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Pal et al. (2010) conducted a cohort in Childhood cancer (n=514). Potentially cardiotoxic therapies (anthracyclines, cardiac irradiation, high-dose cyclophosphamide, or high-dose ifosfamide) was evaluated on Subclinical cardiac dysfunction (left ventricular shortening fraction <30%). Among adult 5-year childhood cancer survivors treated with potentially cardiotoxic therapies, 27% had subclinical cardiac dysfunction (LVSF <30%).
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