Prognostication in Philadelphia Chromosome Negative Myeloproliferative Neoplasms: a Review of the Recent Literature

被引:6
作者
Zhou, Amy [1 ]
Afzal, Amber [1 ]
Oh, Stephen T. [1 ]
机构
[1] Washington Univ, Div Hematol, Sch Med, 660 S Euclid Ave,Campus Box 8125, St Louis, MO 63110 USA
关键词
Myeloproliferative neoplasms; Prognostic factors; INTERNATIONAL WORKING GROUP; BONE-MARROW FIBROSIS; DEFINED ESSENTIAL THROMBOCYTHEMIA; JAK2V617F ALLELE BURDEN; LEUKEMIA-FREE SURVIVAL; POLYCYTHEMIA-VERA; PRIMARY MYELOFIBROSIS; MUTATIONAL STATUS; IPSET-THROMBOSIS; IDIOPATHIC MYELOFIBROSIS;
D O I
10.1007/s11899-017-0401-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The prognosis for patients with Philadelphia chromosome (Ph)-negative myeloproliferative neoplasms (MPNs) is highly variable. All Ph-negative MPNs carry an increased risk for thrombotic complications, bleeding, and leukemic transformation. Several clinical, biological, and molecular prognostic factors have been identified in recent years, which provide important information in guiding management of patients with Ph-negative MPNs. In this review, we critically evaluate the recent published literature and discuss important new developments in clinical and molecular factors that impact survival, disease transformation, and thrombosis in patients with polycythemia vera, essential thrombocythemia, and primary myelofibrosis. Recent studies have identified several clinical factors and non-driver mutations to have prognostic impact on Ph-negative MPNs independent of conventional risk stratification and prognostic models. In polycythemia vera (PV), leukocytosis, abnormal karyotype, phlebotomy requirement on hydroxyurea, increased bone marrow fibrosis, and mutations in ASXL1, SRSF2, and IDH2 were identified as additional adverse prognostic factors. In essential thrombocythemia (ET), JAK2 V617F mutation, splenomegaly, and mutations in SH2B3, SF3B1, U2AF1, TP53, IDH2, and EZH2 were found to be additional negative prognostic factors. Bone marrow fibrosis and mutations in ASXL1, SRSF2, EZH2, and IDH1/2 have been found to be additional prognostic factors in primary myelofibrosis (PMF). CALR mutations appear to be a favorable prognostic factor in PMF, which has not been clearly demonstrated in ET. The prognosis for patients with PV, ET, and PMF is dependent upon the presence or absence of several clinical, biological, and molecular risk factors. The significance of additional risk factors identified in these recent studies will need further validation in prospective studies to determine how they may be best utilized in the management of these disorders.
引用
收藏
页码:397 / 405
页数:9
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