Key result
Serum cardiac Troponin T levels did not differ between patients with normal and abnormal echocardiographic findings following high-dose doxorubicin therapy (P=0.376).
Why the study?
Does serum cTnT correlate with echocardiographic parameters for detecting subclinical doxorubicin-related cardiotoxicity in pediatric and young adult patients?
Cross-Sectional (n=24)
Does serum cTnT correlate with echocardiographic parameters for detecting subclinical doxorubicin-related cardiotoxicity in pediatric and young adult patients?
p-value: p=0.376
Echocardiographic follow-up is more reliable than serum cTnT levels for detecting subclinical cardiac toxicity in patients treated with high-dose doxorubicin.
Serum cTnT may detect subclinical doxorubicin cardiotoxicity; leaves open its clinical utility pending prospective validation.
OBJECTIVE: We investigated the usefulness of serum cardiac Troponin T (cTnT) to detect doxorubicin related cardiotoxicity as a non-invasive and reliable method. PATIENTS AND METHODS: Twenty-four patients who received doxorubicin for their solid tumors at cumulative doses of 400 mg/m(2) or higher, between June 1982 and August 2000, were included in this study. None of them had clinical signs or symptoms of cardiotoxicity. The age range was 3-31 years (median 14), and male to female ratio was 14/10. The systolic and diastolic cardiac functions were evaluated by two-dimensional, M-mode, and Doppler echocardiography. Serum cTnT levels were measured by a third generation immunoassay method and the lowest detectable level was 0.010 ng/ml. RESULTS: The cumulative doxorubicin doses were at the range of 400 and 840 mg/m(2) (median 480). The time past from the last doxorubicin dose was 1-168 months (median 12). All of the patients had normal chest X-rays, electrocardiograms, and nine patients (37.5%) had abnormal systolic or diastolic cardiac function parameters. The median cumulative doxorubicin doses of the patients with normal and abnormal echocardiographic parameters were 480 and 440 mg/m(2), respectively. Serum cTnT values of 21 patients were below the detection limit (< 0.010 ng/ml). There was no statistical difference between serum cTnT levels of the patients with normal and abnormal echocardiographic findings (P = 0.376). CONCLUSIONS: No correlation was found between serum cTnT values, cumulative doxorubicin doses, and systolic or diastolic cardiac functions. We can conclude that echocardiographic follow-up is more reliable than serum cTnT levels for detecting subclinical cardiac toxicity.
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Kısmet et al. (2003) conducted a cross-sectional in Doxorubicin-related cardiotoxicity in solid tumors (n=24). Serum cardiac Troponin T (cTnT) vs. Echocardiography was evaluated on Difference in serum cTnT levels between patients with normal and abnormal echocardiographic findings (p=0.376). Serum cardiac Troponin T levels did not differ between patients with normal and abnormal echocardiographic findings following high-dose doxorubicin therapy (P=0.376).
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