Campbell Peter J, Griesshammer Martin, Döhner Konstanze, Döhner Hartmut, Kusec Rajko, Hasselbalch Hans C, Larsen Thomas Stauffer, Pallisgaard Niels, Giraudier Stéphane, Le Bousse-Kerdilès Marie-Caroline, Desterke Christophe, Guerton Bernadette, Dupriez Brigitte, Bordessoule Dominique, Fenaux Pierre, Kiladjian Jean-Jacques, Viallard Jean-François, Brière Jean, Harrison Claire N, Green Anthony R, Reilly John T
Department of Haematology, University of Cambridge, United Kingdom.
Blood. 2006 Mar 1;107(5):2098-100. doi: 10.1182/blood-2005-08-3395. Epub 2005 Nov 17.
Most patients with polycythemia vera and half with idiopathic myelofibrosis and essential thrombocythemia have an acquired V617F mutation in JAK2. Using sensitive polymerase chain reaction (PCR)-based methods, we genotyped 152 patients with idiopathic myelofibrosis to establish whether there were differences in presentation and outcome between those with and those without the mutation. Patients positive for V617F had higher neutrophil and white cell counts (P = .02) than did patients negative for V617F, but other diagnostic features were comparable between the 2 groups. Patients positive for V617F were less likely to require blood transfusion during follow-up (P = .03). Despite this, patients positive for V617F had poorer overall survival, even after correction for confounding factors (P = .01).
大多数真性红细胞增多症患者以及半数原发性骨髓纤维化和原发性血小板增多症患者的JAK2基因存在获得性V617F突变。我们采用基于聚合酶链反应(PCR)的灵敏方法,对152例原发性骨髓纤维化患者进行基因分型,以确定携带和未携带该突变的患者在临床表现和预后方面是否存在差异。V617F阳性患者的中性粒细胞和白细胞计数高于V617F阴性患者(P = 0.02),但两组的其他诊断特征相当。V617F阳性患者在随访期间需要输血的可能性较小(P = 0.03)。尽管如此,即使校正混杂因素后,V617F阳性患者的总生存期仍较差(P = 0.01)。