Vredenburgh J J, McIntyre O R, Cornwell G G, Ball E D, Cornell C J, Mills L E, O'Donnell J F
Department of Medicine, Dartmouth-Hitchhock Medical Center, Hanover, NH.
Med Pediatr Oncol. 1988;16(3):187-9. doi: 10.1002/mpo.2950160307.
Seventeen patients with relapsed or refractory acute nonlymphocytic leukemia were treated with 14 mg/m2 of mitoxantrone given in a 30-minute infusion daily for three days. If the day fourteen bone marrow showed residual leukemia, a second course was given at the same dose for two days. Eight patients (47%) entered complete remission. Three patients (17%) had a partial response, four (24%) did not respond, and two (12%) died with hypoplastic marrows during treatment. Seven of the 12 relapsed patients entered a complete remission, as did one of the five refractory patients. Toxicity was acceptable; prolonged myelosuppression, moderate hepatic toxicity, and stomatitis were the only problems. Several dose schedules of mitoxantrone have been studied by other investigators with varying results. The three-day schedule in the present study is similar to the schedule used for common induction regimens employing anthracycline drugs. On the basis of its activity and acceptable toxicity in relapsed and refractory ANLL patients, we feel that this schedule could be safely combined with other agents in future studies.
17例复发或难治性急性非淋巴细胞白血病患者接受了米托蒽醌治疗,剂量为14mg/m²,每日静脉输注30分钟,共3天。如果第14天骨髓显示有残留白血病,则以相同剂量再给予一个疗程,为期2天。8例患者(47%)达到完全缓解。3例患者(17%)部分缓解,4例(24%)无反应,2例(12%)在治疗期间死于骨髓增生低下。12例复发患者中有7例达到完全缓解,5例难治性患者中有1例达到完全缓解。毒性反应可以接受;唯一的问题是骨髓抑制时间延长、中度肝毒性和口腔炎。其他研究者对米托蒽醌的几种给药方案进行了研究,结果各异。本研究中的3天给药方案与使用蒽环类药物的常见诱导方案相似。基于其在复发和难治性急性非淋巴细胞白血病患者中的活性和可接受的毒性,我们认为该方案在未来的研究中可以安全地与其他药物联合使用。