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Hematologic and Cytogenetic Findings in Myelodysplastic Syndromes Treated with Recombinant Human Granulocyte Colony‐stimulating Factor

机译:重组人粒细胞集落刺激因子治疗骨髓增生异常综合征的血液学和细胞遗传学发现

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摘要

We administered recombinant human granulocyte colony‐stimulating factor (rhG‐CSF) to four patients with myelodysplastic syndrome (MDS) and three patients with non‐MDS (two malignant lymphoma and one lung cancer) as a part of a phase II trial and analyzed the effects of rhG‐CSF on the neoplastic cells of MDS by performing sequential chromosome analyses on the bone marrow cells. A greater than 3‐fold increase in neutrophil count was observed in the MDS patients after rhG‐CSF infusions, whereas the number of blasts in the bone marrow did not increase and none of them progressed into the leukemic phase. After rhG‐CSF treatment, the bone marrow cells obtained from patients without MDS did not show any particular chromosome abnormalities such as chromosomal breakage. On the contrary, two of the four MDS patients with acquired chromosome abnormalities showed a change in the frequency of marrow cells with clonal abnormalities after rhG‐CSF treatment; the proportion of metaphase cells with additional numerical chromosome abnormalities decreased in these two MDS patients. After discontinuation of the treatment, the constitution of marrow cells with chromosome changes reverted to that before treatment. The remaining two MDS patients did not show any particular chromosome changes after the rhG‐CSF treatment, indicating that rhG‐CSF may not promote the characteristics of dyshematopoiesis in MDS, and act on cells derived from an MDS clone.
机译:作为II期试验的一部分,我们对4例骨髓增生异常综合征(MDS)和3例非MDS患者(2例恶性淋巴瘤和1例肺癌)施用了重组人粒细胞集落刺激因子(rhG-CSF),并分析了通过对骨髓细胞进行顺序染色体分析,rhG-CSF对MDS肿瘤细胞的影响。 rhG-CSF输注后,MDS患者的中性粒细胞计数增加了3倍以上,而骨髓中的胚泡数目却没有增加,并且都没有发展为白血病期。经过rhG-CSF治疗后,未患有MDS的患者的骨髓细胞未显示任何特定的染色体异常,例如染色体断裂。相反,在获得性染色体异常的4名MDS患者中,有2例在rhG-CSF治疗后出现克隆异常的骨髓细胞发生频率改变。在这两名MDS患者中,具有其他数字染色体异常的中期细胞的比例降低了。停止治疗后,具有染色体变化的骨髓细胞的结构恢复为治疗前的状态。其余两名MDS患者在rhG-CSF处理后未显示任何特定的染色体变化,表明rhG-CSF可能不会促进MDS中的血细胞生成异常的特征,并作用于MDS克隆衍生的细胞。

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