Rammeloo L A, Postma A, Sobotka-Plojhar M A, Bink-Boelkens M T, Berg A, Veerman A J, Kamps W A
Children's Cancer Center, University Hospital, Groningen, The Netherlands.
Med Pediatr Oncol. 2000 Jul;35(1):13-9. doi: 10.1002/1096-911x(200007)35:1<13::aid-mpo3>3.0.co;2-g.
To investigate late cardiotoxicity in childhood acute lymphoblastic leukemia (ALL) survivors after induction treatment with or without daunorubicin (DNR; 25 mg/m(2), i.v., weekly, x4, cumulative dose 100 mg/m(2)).
Cardiac function was assessed in 90 event-free survivors of childhood ALL, 11.4-17.8 years (median 14.8 years) after treatment according to the DCLSG protocol ALL V. In this protocol patients were randomized to receive (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 years (median 4.5 years). The cardiac evaluation consisted of a history, physical examination, electrocardiogram (ECG), 24 hr ambulatory ECG, and echocardiography.
Electrocardiographic data, arrhythmias, left ventricular dimensions, left ventricular contractility, wall stress, and diastolic function were within normal limits in both groups. No difference could be shown between data from group A (n = 40) and group B (n = 50).
No late cardiac damage was demonstrated in childhood ALL survivors after induction treatment including a cumulative dose of 100 mg/m(2) DNR, compared to 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 induction treatment of ALL.
研究儿童急性淋巴细胞白血病(ALL)幸存者在接受或不接受柔红霉素(DNR;25mg/m²,静脉注射,每周一次,共4次,累积剂量100mg/m²)诱导治疗后的晚期心脏毒性。
根据DCLSG方案ALL V,对90名儿童ALL无事件幸存者进行心脏功能评估,这些幸存者在治疗后11.4 - 17.8岁(中位年龄14.8岁)。在该方案中,患者被随机分为接受(B组)或不接受(A组)DNR 25mg/m²/周静脉注射,为期诱导治疗的前4周。诊断时年龄为1.2 - 14.9岁(中位年龄4.5岁)。心脏评估包括病史、体格检查、心电图(ECG)、24小时动态心电图和超声心动图。
两组的心电图数据、心律失常、左心室尺寸、左心室收缩性、壁应力和舒张功能均在正常范围内。A组(n = 40)和B组(n = 50)的数据之间未显示出差异。
与接受相同治疗但未使用DNR的幸存者相比,接受包括累积剂量100mg/m² DNR的诱导治疗的儿童ALL幸存者未出现晚期心脏损伤。以每周4次、每次25mg/m²给予100mg/m² DNR似乎是ALL诱导治疗中的安全剂量。