Granulocyte–macrophage colony-stimulating factor (GM-CSF) priming with successive concomitant low-dose Ara-C for elderly patients with secondary/refractory acute myeloid leukemia or advanced myelodysplastic syndrome

被引:0
|
作者
HA Rossi
J O'Donnell
F Sarcinelli
FM Stewart
PJ Quesenberry
PS Becker
机构
[1] University of Massachusetts Medical Center,Division of Hematology and Oncology
[2] Fred Hutchinson Cancer Research Center,Department of Hematology and Oncology
[3] Roger Williams Hospital,Departments of Research and Hematology/Oncology
来源
Leukemia | 2002年 / 16卷
关键词
AML; GM-CSF; MDS; cytarabine; elderly;
D O I
暂无
中图分类号
学科分类号
摘要
Patients with advanced MDS and secondary AML respond poorly to chemotherapy. Granulocyte–macrophage colony-stimulating factor (GM-CSF) can stimulate proliferation of leukemic blasts and sensitize these cells to the cytotoxic effects of S-phase-specific drugs. This is the first report of safety and efficacy of GM-CSF prior to and during cytarabine in a low-dose, intermittent regimen for elderly patients with poor risk acute myelogenous leukemia or myelodysplastic syndrome. Twenty patients, age 68 to 86 years, each received 250 μg/m2 of GM-CSF (Sargramostatin; Immunex, Seattle, WA, USA) subcutaneously (s.c.) or intravenously (i.v.) for 3 days followed by GM-CSF at the same dose and cytarabine 100 mg/m2 i.v. for 3 days. GM-CSF and cytarabine were both administered for 3 days during weeks 2 and 3 followed by a 3-week rest period. Rates of CR and PR were 20% and 40%, respectively. These included clinically significant resolution of cytopenias and transfusion requirements. Many of the responding patients had been heavily pretreated prior to enrollment. One- and 2-year survival estimates are 44% and 19%, respectively. Myelosuppression was the most significant toxicity. Our findings suggest that this novel combination of GM-CSF with sequential and concomitant low-dose cytarabine can benefit patients with poor risk myeloid malignancies.
引用
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页码:310 / 315
页数:5
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