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粒细胞集落刺激因子(G-CSF)治疗后再生障碍性贫血和先天性中性粒细胞减少症患者发生的骨髓发育异常和急性髓系白血病。

Myelodysplasia and acute myeloid leukaemia in cases of aplastic anaemia and congenital neutropenia following G-CSF administration.

作者信息

Imashuku S, Hibi S, Kataoka-Morimoto Y, Yoshihara T, Ikushima S, Morioka Y, Todo S

机构信息

Division of Paediatrics, Children's Research Hospital, Kyoto Prefectural University of Medicine, Japan.

出版信息

Br J Haematol. 1995 Jan;89(1):188-90. doi: 10.1111/j.1365-2141.1995.tb08928.x.

Abstract

Myelodysplasia and acute myeloid leukaemia (MDS/AML) developed in three cases of severe aplastic anaemia (SAA) and one case of congenital neutropenia (CN, Kostmann's disease) who received recombinant human granulocyte colony-stimulating factor (G-CSF) are reported. In these four MDS/AML cases, age at diagnosis of SAA/CN was 0-13 years, the cumulative dose of G-CSF was 98 micrograms/kg to 10 mg/kg over 1-57 months, and the interval from initiation of G-CSF to MDS/AML was 25, 23, 31 and 57 months, respectively. These results suggest a link between SAA/CN and MDS/AML in relation to G-CSF administration; however, large studies are necessary to determine if such a risk is significant in patients with SAA/CN who are treated with G-CSF.

摘要

据报告,3例严重再生障碍性贫血(SAA)患者和1例先天性中性粒细胞减少症(CN, Kostmann病)患者在接受重组人粒细胞集落刺激因子(G-CSF)治疗后发生了骨髓增生异常综合征和急性髓系白血病(MDS/AML)。在这4例MDS/AML病例中,SAA/CN诊断时的年龄为0至13岁,G-CSF的累积剂量在1至57个月内为98微克/千克至10毫克/千克,从开始使用G-CSF到发生MDS/AML的间隔时间分别为25、23、31和57个月。这些结果提示,在使用G-CSF方面,SAA/CN与MDS/AML之间存在联系;然而,需要开展大型研究来确定这种风险在接受G-CSF治疗的SAA/CN患者中是否显著。

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