Rivard G E, Infante-Rivard C, Dresse M F, Leclerc J M, Champagne J
Division of Hematology/Oncology, Hopital Sainte-Justine, Universite de Montreal, Canada.
Chronobiol Int. 1993 Jun;10(3):201-4. doi: 10.3109/07420529309073888.
The evolution of 118 children treated for acute lymphoblastic leukemia between 1976 and 1984, and followed until 1991, was reviewed. Maintenance chemotherapy consisted of daily 6-mercaptopurine (6-MP), weekly methotrexate (MTX), and monthly vincristine and prednisone. Eighty-two children took 6-MP and MTX in the morning, and 36 took them in the evening. Disease-free survival, as determined by Kaplan-Meier analysis, was better for children on evening chemotherapy. Regression analysis (Cox proportional hazards model, with evening versus morning schedule as exposure variable, and age at diagnosis, leucocytosis at diagnosis, and sex as covariates) showed that for those surviving free of disease for longer than 78 weeks, the risk of relapse was 2.56 times greater for the morning schedule than for the evening one.
回顾了1976年至1984年间接受急性淋巴细胞白血病治疗并随访至1991年的118名儿童的病情发展情况。维持化疗包括每日服用6-巯基嘌呤(6-MP)、每周服用甲氨蝶呤(MTX)以及每月服用长春新碱和泼尼松。82名儿童在早晨服用6-MP和MTX,36名儿童在晚上服用。通过Kaplan-Meier分析确定,接受夜间化疗的儿童无病生存率更高。回归分析(Cox比例风险模型,以夜间与早晨化疗方案作为暴露变量,诊断时年龄、诊断时白细胞增多症和性别作为协变量)显示,对于那些无病存活超过78周的儿童,早晨化疗方案的复发风险比晚上化疗方案高2.56倍。