Chronic myeloid neoplasms

被引:0
|
作者
Schmitt-Graeff, A. H. [1 ]
机构
[1] Univ Freiburg Klinikum, Inst Pathol, D-79106 Freiburg, Germany
来源
PATHOLOGE | 2010年 / 31卷 / 01期
关键词
Myeloproliferative neoplasms; Myelodysplastic/myeloproliferative overlap syndromes; Genetics; JAK2V617F mutations; Targeted therapy; WORLD-HEALTH-ORGANIZATION; BONE-MARROW; ESSENTIAL THROMBOCYTHEMIA; SYSTEMIC MASTOCYTOSIS; POLYCYTHEMIA-VERA; LEUKEMIA; MYELOFIBROSIS; CLASSIFICATION; MANAGEMENT; REGRESSION;
D O I
10.1007/s00292-009-1261-x
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Myeloproliferative neoplasms (MPNs) and related chronic disorders constitute a subgroup of myeloid malignancies which are defined according to clinical, morphological and molecular features by the actual World Health Organization classification of tumors of the haematopietic system. Screening procedures for a BCR-ABL fusion gene, JAK2, thrombopoietin receptor and KIT mutations are formally included in the diagnostic approach. Myelodysplastic/MPN overlap syndromes include rare entities such as refractory anemia with ringed sideroblasts characterized by a high proportion of JAK2V617F mutated cases. The paradigm of targeted treatment of chronic myeloid leukemia with imatinib has now been extended to eosinophilia-associated myeloid neoplasms with PDGFRA, PDGFRB or FGFR1 gene mutations. Pegylated interferon-alpha has convincingly been proved to reduce the JAK2 allele burden. JAK2 inhibitor drugs are currently being tested in clinical trials. The development of pathogenesis-targeted diagnostic and therapeutic approaches to the various MPNs will continue in the future.
引用
收藏
页码:29 / 41
页数:13
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