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使用包含中等剂量阿糖胞苷和米托蒽醌的方案对新诊断的急性髓性白血病进行强化巩固化疗。

Intensive consolidation chemotherapy for newly diagnosed acute myeloid leukemia using a regime containing moderate dose cytosine arabinoside and mitoxantrone.

作者信息

Liang R, Chan T K, Chu Y C, Chan J, Chan C H, Chiu E, Lie A, Kwong Y L, Yeung Y M, Chan L C

机构信息

Department of Medicine, Queen Mary Hospital, Hong Kong.

出版信息

Anticancer Drugs. 1995 Apr;6(2):224-8. doi: 10.1097/00001813-199504000-00005.

Abstract

Fifty patients with previously untreated acute myeloid leukemia were treated with an induction regimen consisting of cytosine arabinoside 100 mg/m2 per day by 18 h i.v. infusion for 7 days, daunorubicin 50 mg/m2 per day by i.v. bolus injection for 3 days and etoposide 75 mg/m2 per day by 1 h i.v. infusion for 7 days. Thirty seven of them (74%) went into complete remission (CR) and they all then received two consecutive courses of consolidation chemotherapy consisting of cytosine arabinoside 500 mg/m2 per day by 1 h i.v. infusion every 12 h for 4 days (total eight doses) and mitoxantrone 12 mg/m2 daily by 30 min i.v. infusion for 3 days. They were followed by maintenance chemotherapy with cytosine arabinoside and thioguanine 2 monthly. With a median follow up time of 24 months, 20 of the 37 complete responders had relapsed (54%). The disease-free survival (DFS) of 37 CR patients and the overall survival of all patients at 24 months were 37 and 44%, respectively. Age of patients and number of courses of induction chemotherapy to achieve CR were significant factors predicting DFS. Myelosuppression was the major toxic side effects. Ten patients had prolonged marrow suppression following consolidation chemotherapy. In conclusion, despite the significant myelosuppression observed, overall improvement in treatment outcome was not demonstrable with the use of this intensive consolidation therapy.

摘要

50例既往未经治疗的急性髓系白血病患者接受了诱导治疗方案,该方案包括:阿糖胞苷100mg/m²,静脉滴注18小时,持续7天;柔红霉素50mg/m²,静脉推注,持续3天;依托泊苷75mg/m²,静脉滴注1小时,持续7天。其中37例(74%)达到完全缓解(CR),随后他们均接受了两个连续疗程的巩固化疗,巩固化疗方案为:阿糖胞苷500mg/m²,每12小时静脉滴注1小时,持续4天(共8剂),米托蒽醌12mg/m²,静脉滴注30分钟,持续3天。之后他们接受了阿糖胞苷和硫鸟嘌呤每月一次的维持化疗。中位随访时间为24个月,37例完全缓解者中有20例复发(54%)。37例CR患者的无病生存期(DFS)和所有患者24个月时的总生存期分别为37%和44%。患者年龄和达到CR所需的诱导化疗疗程数是预测DFS的重要因素。骨髓抑制是主要的毒副作用。10例患者在巩固化疗后出现骨髓抑制延长。总之,尽管观察到明显的骨髓抑制,但使用这种强化巩固治疗并未显示出治疗效果的整体改善。

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