Is there a potential role for serum cardiac troponin I as a marker for myocardial dysfunction in pediatric patients receiving anthracycline-based therapy? A pilot study

Citation
P. Mathew et al., Is there a potential role for serum cardiac troponin I as a marker for myocardial dysfunction in pediatric patients receiving anthracycline-based therapy? A pilot study, CANCER INV, 19(4), 2001, pp. 352-359
Citations number
42
Language
INGLESE
art.tipo
Article
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
CANCER INVESTIGATION
ISSN journal
0735-7907 → ACNP
Volume
19
Issue
4
Year of publication
2001
Pages
352 - 359
Database
ISI
SICI code
0735-7907(2001)19:4<352:ITAPRF>2.0.ZU;2-J
Abstract
Serum cardiac troponin I (cTnI) levels have been reported to have high spec ificity and sensitivity to acute myocardial infarction and coronary ischemi c syndromes in adult patients. Our goal was to evaluate the usefulness of s erum cTnI in the early diagnosis of cardiac injury from anthracyclines, and to compare these values with echocardiographic findings of cardiac dysfunc tion. In this prospective study, children being treated on several Children 's Cancer Group protocols underwent measurement of shortening fraction (SF) , ejection fraction (EF), and serum cTnI levels prior to anthracycline ther apy. Sequential serum cTnI levels were then measured along with regularly s cheduled echocardiograms with progressively increasing doses of anthracycli nes. Fifteen children with median age of 5.75 years (range, 15 months to 15 .5 years) at diagnosis were evaluated. Anthracycline doses range from 11.72 mg/kg (in patients <3 years of age) to 375 mg/m(2). All but one patient ha d normal cTnI levels. His level measured at 1.7 ng/ml after 315 mg/m(2), bu t was normal on follow-up testing. Initial SF ranged from 32 to 48%, and EF from 60 to 80%. On follow-up, SF and EF ranged from 30 to 41% and 55 to 70 %, respectively. Both SF and EF were significantly lower (p < 0.001) as com pared to the initial values. Despite this, all patients remained clinically asymptomatic from the cardiac standpoint. We did not observe elevations of serum cTnI levels in clinically asymptomatic children who receive anthracy cline therapy up to doses of 375 mg/m(2.) Does this mean that cardiac injur y has not occurred? The possibility of assay sensitivity and the timing of serum sampling and echocardiograms may be important. In addition, larger sa mple size or longer follow-up may be helpful to determine if higher doses o r symptomatic patients potentially have elevation in cTnI levels.