Transient hematologic and clinical effect of E21R in a child with end-stage juvenile myelomonocytic leukemia

被引:21
作者
Bernard, F
Thomas, C
Emile, JF
Hercus, T
Cassinat, B
Chomienne, C
Donadieu, J
机构
[1] CHU Montpellier, Hemato Oncol Unit, Dept Pediat, Montpellier, France
[2] Hop Paul Brousse, Dept Pathol, Villejuif, France
[3] CHU Nantes, Pediat Hemato Oncol Dept, F-44035 Nantes 01, France
[4] Hanson Inst, Cytokine Receptor Lab, Adelaide, SA, Australia
[5] Hop St Louis, Lab Biol Hematopoiet Cells, Paris, France
[6] Hop Trousseau, Pediat Hematol Oncol Dept, F-75571 Paris, France
关键词
D O I
10.1182/blood.V99.7.2615
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
E21R is a modified granulocyte macrophage-colony-stimulating factor (GMCSF) protein which results in antagonism of GM-CSF function via selective binding to the GM-CSF receptor complex. Juvenile chronic myelomonocytic leukemia (JMML) is a rare leukemia where spontaneous proliferation of myeloid and monocytic precursors in patients' bone marrow cultures is dependent on GM-CSF. For patients who progress after systemic chemotherapy, there are no effective therapies. In, vitro and in vivo studies in an animal model demonstrating that E21R exerts an antileukemic action prompted us to consider its:potential utility in a child with end-stage JMML. E21R was well-tolerated during the 3 courses of subcutaneous treatment. A clear in vivo efficacy was observed after 2 courses of E21R but the disease appeared completely refractory during the third course. This novel therapeutic approach clearly deserves further evaluation in JMML. (C) 2002 by The American Society of Hematology.
引用
收藏
页码:2615 / 2616
页数:2
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