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切断与骨髓增生异常综合征的联系:慢性粒单核细胞白血病的特异性生物学及管理策略

Cutting the cord from myelodysplastic syndromes: chronic myelomonocytic leukemia-specific biology and management strategies.

作者信息

Padron Eric, Steensma David P

机构信息

aH. Lee Moffitt Cancer Center, Tampa, Florida bDana-Farber Cancer Institute, Boston, Massachusetts, USA.

出版信息

Curr Opin Hematol. 2015 Mar;22(2):163-70. doi: 10.1097/MOH.0000000000000112.

Abstract

PURPOSE OF REVIEW

Chronic myelomonocytic leukemia (CMML) is a troublesome hematologic malignancy characterized by peripheral blood monocytosis, marrow dysplasia, cytopenias, frequent extramedullary involvement by clonal cells, and a propensity for progression to acute myeloid leukemia. Although previously considered a subtype of the myelodysplastic syndromes (MDS), CMML is now recognized as a distinct entity with unique biologic and clinical features. This change has created a scientific and clinical research landscape that makes it difficult to discern CMML-specific validated conclusions versus speculative extrapolation from more general MDS data.

RECENT FINDINGS

Here, we review recent biologic observations that support the current CMML WHO classification, such as the high frequency of SRSF2 and ASXL1 mutations compared with MDS and critical dependence of CMML cells on granulocyte-macrophage colony-stimulating factor signaling. In addition, we discuss CMML-specific prognostic tools and therapeutic results of agents developed for MDS in patients with CMML.

SUMMARY

The present review focuses on evidence supporting CMML ontology and identifies key clinical differences in the management of CMML and that of MDS subtypes.

摘要

综述目的

慢性粒单核细胞白血病(CMML)是一种棘手的血液系统恶性肿瘤,其特征为外周血单核细胞增多、骨髓发育异常、血细胞减少、克隆细胞频繁髓外浸润以及进展为急性髓系白血病的倾向。尽管CMML以前被认为是骨髓增生异常综合征(MDS)的一个亚型,但现在它被公认为是一种具有独特生物学和临床特征的独立疾病实体。这一变化创造了一个科学和临床研究格局,使得很难区分CMML特异性的已验证结论与从更一般的MDS数据进行的推测性推断。

最新发现

在此,我们回顾了支持当前CMML世界卫生组织分类的近期生物学观察结果,例如与MDS相比,SRSF2和ASXL1突变的高频率以及CMML细胞对粒细胞-巨噬细胞集落刺激因子信号传导的关键依赖性。此外,我们讨论了CMML特异性的预后工具以及为MDS开发的药物在CMML患者中的治疗结果。

总结

本综述重点关注支持CMML本体论的证据,并确定CMML与MDS亚型管理中的关键临床差异。

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