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[大剂量阿糖胞苷联合米托蒽醌治疗儿童急性髓系白血病。AML BFM - 85复发研究的初步结果]

[High dosage ARA-C in combination with mitoxantrone in therapy of acute myeloid leukemia in childhood. Initial results of the AML BFM-85 recurrence study].

作者信息

Ritter J, Creutzig U, Henze G, Jürgens H, Bode U, Prindull G, Schellong G

出版信息

Onkologie. 1987 Feb;10(1):24-7. doi: 10.1159/000216363.

Abstract

19 children with AML were treated using the combination of high dose cytosine-arabinoside and mitoxantrone. All children were initially treated according to protocol AML-BFM-83. 6 children with refractory AML, 9 children with bone-marrow relapse during or after maintenance therapy and 4 children with residual blasts (5-25%) after remission induction and consolidation therapy AML-BFM 83 were treated with the relapse protocol. 6 of 15 children with refractory AML and all 4 children with residual blasts achieved a complete remission. 2 children died in bone-marrow aplasia and 1 child did not respond. One child died after further mitoxantrone treatment due to toxic cardiomyopathy. All children went into severe bone marrow aplasia, which lasted in median 27 days. These data indicate a high antileukemic activity of HD-ARA C/mitoxantrone in childhood AML.

摘要

19例急性髓系白血病患儿采用大剂量阿糖胞苷与米托蒽醌联合治疗。所有患儿最初均按照AML-BFM-83方案进行治疗。6例难治性急性髓系白血病患儿、9例维持治疗期间或之后出现骨髓复发的患儿以及4例诱导缓解和巩固治疗AML-BFM 83后仍有残留原始细胞(5%-25%)的患儿接受了复发方案治疗。15例难治性急性髓系白血病患儿中有6例以及所有4例有残留原始细胞的患儿均实现了完全缓解。2例患儿死于骨髓再生障碍,1例患儿无反应。1例患儿在进一步接受米托蒽醌治疗后因中毒性心肌病死亡。所有患儿均出现严重骨髓再生障碍,持续时间中位数为27天。这些数据表明HD-ARA C/米托蒽醌在儿童急性髓系白血病中具有较高的抗白血病活性。

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