Clinical management of myelodysplastic syndrome/myeloproliferative neoplasm overlap syndromes

被引:10
作者
Clara, Joseph A. [1 ]
Sallman, David A. [2 ]
Padron, Eric [2 ]
机构
[1] Univ S Florida, Dept Internal Med, Morsani Coll Med, Tampa, FL 33606 USA
[2] H Lee Moffitt Canc Ctr & Res Inst, Malignant Hematol Program, Tampa, FL 33612 USA
关键词
Myelodysplastic syndromes; myeloproliferative neoplasms; next-generation sequencing; CMML; aCML; JMML; MDS/MPN-U; CHRONIC MYELOMONOCYTIC LEUKEMIA; STEM-CELL TRANSPLANTATION; CHRONIC MYELOID-LEUKEMIA; CHRONIC NEUTROPHILIC LEUKEMIA; CHRONIC MYELOGENOUS LEUKEMIA; ACQUIRED UNIPARENTAL DISOMY; RING SIDEROBLASTS; MYELODYSPLASTIC/MYELOPROLIFERATIVE NEOPLASMS; REFRACTORY-ANEMIA; SETBP1; MUTATIONS;
D O I
10.20892/j.issn.2095-3941.2016.0043
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The myelodysplastic/myeloproliferative neoplasms (MDS/MPNs) are a unique group of hematologic malignancies characterized by concomitant myelodysplastic and myeloproliferative features. According to the 2008 WHO classification, the category includes atypical chronic myeloid leukemia (aCML), chronic myelomonocytic leukemia (CMML), juvenile myelomonocytic leukemia (JMML), MDS/MPN-unclassifiable (MDS/MPN-U), and the provisional entity refractory anemia with ring sideroblasts and thrombocytosis (RARS-T). Although diagnosis currently remains based on clinicopathologic features, the incorporation of next generation platforms has allowed for the recent molecular characterization of these diseases which has revealed unique and complex mutational profiles that support their distinct biology and is anticipated to soon play an integral role in diagnosis, prognostication, and treatment. Future goals of research should include the development of disease-modifying therapies, and further genetic understanding of the category will likely form the foundation of these efforts.
引用
收藏
页码:360 / 372
页数:13
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