Division of Hematology and Medical Oncology, Department of Medicine, Weill Cornell Medical College, New York, NY 10065-4896, USA.
Leuk Res. 2011 Feb;35(2):177-82. doi: 10.1016/j.leukres.2010.06.017. Epub 2010 Jul 22.
In a series of 105 patients with polycythemia vera, we retrospectively determined whether the JAK2(V617F) mutation correlated with severity of disease phenotype. Higher JAK2(V617F) allele burden correlated with more advanced myelofibrosis, greater splenomegaly, and higher white blood cell count, but not with age, gender, hematocrit level, or frequency of phlebotomy prior to cytoreductive therapy. Although a subgroup at increased risk for thrombosis was not clearly defined, there was a suggestion that frequency of thrombosis increased as the JAK2(V617F) allele burden increased. The JAK2(V617F) allele burden did not change significantly in treated patients with serial JAK2 analyses.
在 105 例真性红细胞增多症患者中,我们回顾性地确定了 JAK2(V617F)突变是否与疾病表型的严重程度相关。较高的 JAK2(V617F)等位基因负担与更严重的骨髓纤维化、更大的脾肿大和更高的白细胞计数相关,但与年龄、性别、血细胞比容水平或细胞减少治疗前放血的频率无关。尽管没有明确定义一个具有更高血栓形成风险的亚组,但有迹象表明,随着 JAK2(V617F)等位基因负担的增加,血栓形成的频率增加。在接受连续 JAK2 分析的治疗患者中,JAK2(V617F)等位基因负担没有显著变化。