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重组人粒细胞集落刺激因子和促红细胞生成素对骨髓增生异常综合征贫血的维持治疗:体内协同作用的证据

Maintenance treatment of the anemia of myelodysplastic syndromes with recombinant human granulocyte colony-stimulating factor and erythropoietin: evidence for in vivo synergy.

作者信息

Negrin R S, Stein R, Doherty K, Cornwell J, Vardiman J, Krantz S, Greenberg P L

机构信息

Department of Medicine, Stanford University Medical Center, CA 94305, USA.

出版信息

Blood. 1996 May 15;87(10):4076-81.

PMID:8639764
Abstract

Patients with myelodysplastic syndromes (MDS) have refractory cytopenias leading to transfusion requirements and infectious complications. In vitro marrow culture data have indicated that granulocyte colony stimulating factor (G-CSF) synergizes with erythropoietin (EPO) for the production of erythroid precursors. In an effort to treat the anemia and neutropenia in this disorder, MDS patients were treated with a combination of recombinant human EPO and recombinant human G-CSF. Fifty-five patients were enrolled in the study of which 53 (96%) had a neutrophil response. Forty-four patients were evaluable for an erythroid response of which 21 (48%) responded. An erythroid response was significantly more likely in those patients with relatively low serum EPO levels, higher absolute basal reticulocyte counts and normal cytogenetics at study entry. Seventeen (81%) of the patients who responded to combined G-CSF plus EPO therapy continued to respond during an 8-week maintenance phase. G-CSF was then discontinued and all patients' neutrophil responses were diminished, whereas 8 continued to have an erythroid response to EPO alone. In 7 of the remaining 9 patients, resumption of G-CSF was required for recurrent erythroid responses. The median duration of erythroid responses to these cytokines was 11 months, with 6 patients having relatively prolonged and durable responses for 15 to 36 months. Our results also indicate that approximately one half of responding patients require both G-CSF and EPO to maintain an effective erythroid response, suggesting that synergy between G-CSF and EPO exists in vivo for the production of red blood cells in MDS.

摘要

骨髓增生异常综合征(MDS)患者存在难治性血细胞减少,导致需要输血以及出现感染并发症。体外骨髓培养数据表明,粒细胞集落刺激因子(G-CSF)与促红细胞生成素(EPO)协同作用可促进红系祖细胞的生成。为了治疗该疾病中的贫血和中性粒细胞减少,MDS患者接受了重组人EPO和重组人G-CSF联合治疗。55例患者纳入研究,其中53例(96%)出现中性粒细胞反应。44例患者可评估红系反应,其中21例(48%)有反应。在研究开始时血清EPO水平相对较低、绝对基础网织红细胞计数较高且细胞遗传学正常的患者中,出现红系反应的可能性显著更高。17例(81%)对G-CSF加EPO联合治疗有反应的患者在8周维持期内持续有反应。然后停用G-CSF,所有患者的中性粒细胞反应均减弱,而8例患者继续对单独使用的EPO有红系反应。在其余9例患者中的7例中,复发的红系反应需要恢复使用G-CSF。这些细胞因子诱导红系反应的中位持续时间为11个月,6例患者有相对延长且持久的反应,持续15至36个月。我们的结果还表明,约一半有反应的患者需要G-CSF和EPO两者来维持有效的红系反应,这表明G-CSF和EPO在体内对MDS患者红细胞生成存在协同作用。

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