Wolanskyj Alexandra P, Lasho Terra L, Schwager Susan M, McClure Rebecca F, Wadleigh Martha, Lee Stephanie J, Gilliland D Gary, Tefferi Ayalew
Division of Hematology, Mayo Clinic, Rochester, MN 55905, USA.
Br J Haematol. 2005 Oct;131(2):208-13. doi: 10.1111/j.1365-2141.2005.05764.x.
Clinical correlates and long-term prognostic relevance of the JAK2(V617F) mutation was studied in 150 patients with essential thrombocythaemia (ET) from a single institution and followed for a median of 11.4 years. During this period, thrombotic complications were documented in 62 patients (41.3%) and transformation into acute myeloid leukaemia (AML), polycythaemia vera (PV), or myelofibrosis with myeloid metaplasia (MMM) occurred in 4 (2.7%), 8 (5.3%), and 15 (10%) patients, respectively. JAK2(V617F) was detected in either archived bone marrow or blood cells from 73 patients (48.7%) but none were homozygous for the mutant allele. Parameters at diagnosis that were significantly associated with the presence of JAK2(V617F) included advanced age and higher counts of both haemoglobin and leucocytes. During follow-up, patients with the mutation were more likely to transform into PV but the incidences of AML, MMM, or thrombotic events were similar between patients with and without the mutation. Multivariate analysis identified advanced age, higher haemoglobin level, and thrombosis history but not the presence of JAK2(V617F) as independent predictors of inferior survival. Therefore, although the presence of JAK2(V617F) in ET appears to promote a PV phenotype, it might not carry treatment-relevant information.
在一家机构的150例原发性血小板增多症(ET)患者中研究了JAK2(V617F)突变的临床相关性及其长期预后意义,并对患者进行了中位时间为11.4年的随访。在此期间,62例患者(41.3%)记录有血栓形成并发症,分别有4例(2.7%)、8例(5.3%)和15例(10%)患者转化为急性髓系白血病(AML)、真性红细胞增多症(PV)或骨髓纤维化伴髓外化生(MMM)。在73例患者(48.7%)的存档骨髓或血细胞中检测到JAK2(V617F),但均无突变等位基因纯合子。诊断时与JAK2(V617F)存在显著相关的参数包括高龄以及血红蛋白和白细胞计数较高。在随访期间,有该突变的患者更有可能转化为PV,但有和没有该突变的患者之间AML、MMM或血栓形成事件的发生率相似。多变量分析确定高龄、较高的血红蛋白水平和血栓形成病史而非JAK2(V617F)的存在是生存较差的独立预测因素。因此,虽然ET中JAK2(V617F)的存在似乎促进PV表型,但它可能不携带与治疗相关的信息。