A. Schiavetti et al., USE OF ICRF-187 FOR PREVENTION OF ANTHRACYCLINE CARDIOTOXICITY IN CHILDREN - PRELIMINARY-RESULTS, Pediatric hematology and oncology, 14(3), 1997, pp. 213-222
The objective of this study is to assess the efficacy of ICRF-187 as a
protective agent against anthracycline cardiotoxicity. Cardiac functi
on was evaluated by echocardiography before and after each cycle of an
thracycline chemotherapy associated with ICRF-187 and compared with th
at of a second group receiving anthracycline chemotherapy without ICRF
-187. The patients were a group of 15 consecutive children affected wi
th various types of solid tuners who were treated with either doxorubi
cin-daunomycin or epirubicin (average doses 340 and 280 mg/m(2), respe
ctively), and treatment was associated with ICRF-187. A second group o
f 15 consecutive children affected With different malignancies werre s
imultaneously treated with either doxorubicin-daunomycin or epirubicin
(average doses 309 and 270 mg/m(2), respectively), but without ICRF-1
87 association. None of the patients treated with anthracyclines and I
CRF-187 association showed abnormalities on echocardiographic examinat
ion. In the second group of patients treated with anthracyclines but w
ithout ICRF-187 association, we observed a decrease in the left ventri
cular ejection fraction to <55% and a decrease in the left ventricular
fractional shortening to <28% in two patients (13.3%). One of these (
6.6%) showed a dilatative cardiomyopathy. Both groups of patients were
treated with low doses of anthracyclines. Although this study was not
randomized, in patients without ICRF-87 cardioprotection, there was a
trend for a worse evolution with one case of clinical cardiomyopathy
as well as subclinical cardiac abnormalities.