LATE CARDIAC TOXICITY OF DOXORUBICIN, EPIRUBICIN, AND MITOXANTRONE THERAPY FOR HODGKINS-DISEASE IN ADULTS

Citation
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
Citations number
NO
Categorie Soggetti
Hematology
Journal title
ISSN journal
10428194
Volume
11
Issue
3-4
Year of publication
1993
Pages
275 - 279
Database
ISI
SICI code
1042-8194(1993)11:3-4<275:LCTODE>2.0.ZU;2-#
Abstract
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.