A. Aviles et al., LATE CARDIAC TOXICITY OF DOXORUBICIN, EPIRUBICIN, AND MITOXANTRONE THERAPY FOR HODGKINS-DISEASE IN ADULTS, Leukemia & lymphoma, 11(3-4), 1993, pp. 275-279
Cardiotoxicity is a well recognized side effect of anthracyclines (dox
orubicin and epirubicin) or antracenadiones (mitoxantrone) at cumulati
ve or high doses. However the side effects have not been evaluated in
adults with Hodgkin's disease who received therapeutic doses of these
drugs. We analyzed the cardiac function studying the left ventricular
ejection fraction (LVEF) at rest in 136 patients with Hodgkin's diseas
e treated with doxorubicin, epirubicin or mitoxantrone used in combina
tion with vinblastine, bleomycin and decarbazine. No other risk factor
s, such as radiation therapy to the mediastinum, were considered. The
follow-up is 5 to 8 years for patients in complete remission. Forty-fi
ve patients received doxorubicin (from 325 to 685 mg/m2, median 475 mg
/m2), 51 patients received epirubicin (from 310 to 610 mg/m2, median 5
10 mg/m2) and 40 patients were treated with mitoxantrone (from 70 to 1
65, median 125 mg/m2). The median time between the end of treatment an
d the evaluation was 6.7 years. Thirty seven percent of the patients (
similar rates in the three groups) showed abnormalities in the LVEF wi
th decreased rates independent of the drug dosage. These were compared
with two control groups, 46 patients treated with the MOPP combinatio
n (mechlorethamine, vincristine, prednisone and procarbazine) or LOPP
(chlorambucil, for mechlorethamine) and 35 healthy volunteers. We beli
eve that the use of anthracyclines or antracenadione will produce late
cardiac effects in a fraction of patients independently of the doses
used and that the indications for these drugs be carefully monitoring
so as to evaluate the development of late side effects.