Why the study?
Does cisplatin-based combination chemotherapy cause early sub-clinical deterioration of cardiac function in patients with testicular cancer?
Does cisplatin-based combination chemotherapy cause early sub-clinical deterioration of cardiac function in patients with testicular cancer?
Cisplatin-based chemotherapy for testicular cancer is associated with early, sub-clinical deterioration of diastolic cardiac function and increased NT-proBNP levels within one year of treatment.
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Supports surveillance for diastolic dysfunction after cisplatin in testicular cancer; leaves open links to clinical events.
Long-term cardiovascular morbidity is increasingly observed in chemotherapy-treated testicular cancer survivors, but little is known of early sub-clinical changes in cardiac function. We prospectively evaluated cardiac function in testicular cancer patients by echocardiography. Systolic (Wall Motion Score Index) and diastolic (E/A-ratio and Tissue Velocity Imaging (TVI)) parameters, and serum levels of N-Terminal pro-Brain Natriuretic Peptide (NT-proBNP) were assessed before the start of chemotherapy and 1 year later. Echocardiography data were compared with an age-matched group of healthy controls. Forty-two patients treated with bleomycin, etoposide and cisplatin were evaluated (median age 27 years, range 18-50). Systolic function and E/A-ratio did not change, whereas the median TVI decreased (12.0 vs 10.0 cms(-1); P=0.002). Median levels of NT-proBNP increased (5 vs 18 pmoll(-1), P=0.034). Compared with controls, TVI before the start of chemotherapy was not significantly different. In conclusion, we found that at a median of 10 months after cisplatin-based treatment for testicular cancer, TVI decreased significantly, indicating a deterioration of diastolic cardiac function. Serum levels of NT-proBNP increased. The prognostic significance of these changes for future cardiovascular morbidity is not clear.
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Altena et al. (2009) studied this question.
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