Braun Theodore P, Maxson Julia E, Agarwal Anupriya, Dunlap Jennifer, Spurgeon Stephen E, Traer Elie
Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97239, USA ; MD/PhD Program.
Knight Cancer Institute, Oregon Health & Science University, Portland, OR 97239, USA.
Leuk Res Rep. 2014 Dec 25;4(1):8-11. doi: 10.1016/j.lrr.2014.12.003. eCollection 2015.
Myeloproliferative neoplasms transformed into AML usually have a poor prognosis. We report a case of essential thrombocythemia with myelofibrosis that transformed into acute promyelocytic leukemia (APL) with both the t(15;17) translocation as well as the JAK2 V617F mutation. Clinically, this case was notable for severe differentiation syndrome despite treatment with high-dose dexamethasone. Cytokine production by differentiating APL cells was not directly abrogated by JAK2 inhibitors in vitro, suggesting that JAK2 V617F enhances the hyperinflammatory response downstream of cytokines. JAK1/2 inhibitors may therefore dampen the inflammatory cascade downstream of cytokine production, similar to glucocorticoids, and have a role in treating severe differentiation syndrome.
骨髓增殖性肿瘤转化为急性髓系白血病通常预后较差。我们报告一例原发性血小板增多症合并骨髓纤维化转化为急性早幼粒细胞白血病(APL)的病例,该病例同时存在t(15;17)易位以及JAK2 V617F突变。临床上,尽管使用了大剂量地塞米松治疗,该病例仍以严重分化综合征为显著特征。在体外,JAK2抑制剂并不能直接消除分化中的APL细胞产生的细胞因子,这表明JAK2 V617F增强了细胞因子下游的过度炎症反应。因此,JAK1/2抑制剂可能会像糖皮质激素一样抑制细胞因子产生下游的炎症级联反应,并在治疗严重分化综合征中发挥作用。