Low-dose daunorubicin in induction treatment of childhood acute lymphoblastic leukemia: No long-term cardiac damage in a randomized study of the Dutch Childhood Leukemia Study Group

Citation
Laj. Rammeloo et al., Low-dose daunorubicin in induction treatment of childhood acute lymphoblastic leukemia: No long-term cardiac damage in a randomized study of the Dutch Childhood Leukemia Study Group, MED PED ONC, 35(1), 2000, pp. 13-19
Citations number
42
Categorie Soggetti
Pediatrics
Journal title
MEDICAL AND PEDIATRIC ONCOLOGY
ISSN journal
00981532 → ACNP
Volume
35
Issue
1
Year of publication
2000
Pages
13 - 19
Database
ISI
SICI code
0098-1532(200007)35:1<13:LDIITO>2.0.ZU;2-Q
Abstract
Background. To investigate late cardiotoxicity in childhood acute lymphobla stic leukemia (ALL) survivors after induction treatment with or without dau norubicin (DNR; 25 mg/m(2), i.v., weekly, x4, cumulative dose 100 mg/m(2)). Procedure, Cardiac function was assessed in 90 event-free survivors of chi ldhood ALL, 11.4-17.8 years (median 14.8 years) after treatment according t o the DCLSG protocol ALL V. In this protocol patients were randomized to re ceive (group B) or not to receive (group A) DNR 25 mg/m(2)/week i.v. during the first 4 weeks of induction treatment. Age at diagnosis was 1.2-14.9 ye ars (median 4.5 years). The cardiac evaluation consisted of a history, phys ical examination, electrocardiogram (ECC), 24 hr ambulatory EGG, and echoca rdiography. Results. Electrocardiographic data, arrhythmias, left ventricul ar dimensions, left ventricular contractility, wall stress, and diastolic f unction were within normal limits in both groups. No difference could be sh own between data from group A (n = 40) and group B (n = 50). Conclusions. N o late cardiac damage was demonstrated in childhood ALL survivors after ind uction treatment including a cumulative dose of 100 mg/m(2) DNR, compared t o survivors who received the same treatment but without DNR. DNR 100 mg/m(2 ) given in 4 doses of 25 mg/m(2)/week appears to be a safe dose in inductio n treatment of ALL. 2000 Wiley-Liss, Inc.