Erythroblastic and/or megakaryoblastic leukemia in Down syndrome: Treatment with low-dose arabinosyl cytosine

被引:25
作者
Tchernia, G
Lejeune, F
Boccara, JF
Denavit, MF
Dommergues, JP
Bernaudin, F
机构
[1] DEPT PEDIAT, F-94270 LE KREMLIN BICETRE, FRANCE
[2] DEPT PEDIAT, CRETEIL, FRANCE
[3] DEPT HEMATOL, BONDY, FRANCE
[4] ST VINCENT DE PAUL, DEPT PEDIAT, PARIS, FRANCE
[5] DEPT PEDIAT, DREUX, FRANCE
[6] DEPT PEDIAT, LE KREMLIN BICETRE, FRANCE
关键词
megakaryoblastic leukemia; Down syndrome; arabinosyl cytosine;
D O I
10.1097/00043426-199602000-00011
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: We report here the clinical response to low-dose arabinosyl cytosine (Ara-C) in seven children with Down syndrome (DS) and acute leukemia in which blast cells express markers of erythroid and/or megakaryoblastic lineages. Following an initial course of treatment with Ara-C, complete remission was obtained in all seven patients. Maintenance therapy with Ara-C was continued during complete remission. Four patients subsequently relapsed; the three others are disease-free. Based on these data, we suggest that when conventional therapy is contraindicated by associated malformations, low-dose Ara-C can be used for treating DS patients with erythroblastic or megakaryoblastic leukemia. The aim of this study was to assess the efficacy of low-dose Ara-C in treating megakaryoblastic and/or erythroblastic leukemia associated with DS. Patients and Methods: Seven patients with DS presented with leukemia in which blast cells displayed early markers of the erythroblastic and/or megakaryoblastic lineage. Low-dose subcutaneous Ara-C (10 mg/m(2) two times per day) was given for 21 days as induction therapy, followed by a 5-10-day course each month for 2 years as a maintenance treatment. Results: Low-dose Ara-C treatment resulted in complete remission in all seven patients and in long-term disease-free survival in three patients. Conclusion: In cases in which conventional chemotherapy is contraindicated, low-dose Ara-C should be considered as a therapeutic alternative for treatment of DS-associated erythroblastic or megakaryocytic leukemia.
引用
收藏
页码:59 / 62
页数:4
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