Matthews R N, Colebatch J H
Arch Dis Child. 1972 Apr;47(252):272-7. doi: 10.1136/adc.47.252.272.
Fifty children with acute leukaemia (44 lymphatic, 6 myeloid) were treated with daunorubicin. In 3 cases, it was given in courses of daily injections; in 47, single injections were given at 7- to 14-day intervals. On the latter (intermittent) regimen, in combination with prednisolone, a good response—complete, bone marrow, or clinical remission—occurred in 22 of 27 cases (81%) of `new' or previously untreated acute lymphoblastic leukaemia but in only 3 of 13 cases previously treated with other drugs. With acute myeloid leukaemia a good response occurred only when daunorubicin was given in combination with other cytotoxic drugs. The major side-effect was bone marrow depression with the related complications of haemorrhage and infection. Cardiotoxicity was not a problem; the cumulative total dose of daunorubicin did not exceed 26·8 mg/kg. This study indicates that intermittent dosage with 2-3 mg/kg at intervals of 7 to 14 days is as effective as, and no more toxic than, the courses of daily injections that have been commonly used.
五十名急性白血病患儿(44例淋巴性白血病,6例髓性白血病)接受了柔红霉素治疗。其中3例采用每日注射疗程给药;47例每隔7至14天进行单次注射。在后者(间歇)治疗方案中,联合泼尼松龙,27例“新”发或既往未治疗的急性淋巴细胞白血病中有22例(81%)出现了良好反应——完全缓解、骨髓缓解或临床缓解,但在13例既往接受过其他药物治疗的病例中仅有3例出现良好反应。对于急性髓性白血病,仅当柔红霉素与其他细胞毒性药物联合使用时才会出现良好反应。主要副作用是骨髓抑制以及与之相关的出血和感染并发症。心脏毒性并非问题;柔红霉素的累积总剂量未超过26.8毫克/千克。本研究表明,每隔7至14天给予2至3毫克/千克的间歇剂量与常用的每日注射疗程效果相同,且毒性并不更高。