Peking University People's Hospital, Peking University Institute of Hematology, Beijing, China.
Leuk Res. 2013 Jun;37(6):624-30. doi: 10.1016/j.leukres.2013.02.007. Epub 2013 Mar 6.
To explore the prognostic value of CD34 expression in NPM1-mutated acute myeloid leukemia (NPM1m+AML), seventy-one NPM1m+AML patients were retrospectively analyzed. The patients with >7% CD34 expression (according to the ROC analysis) had a lower complete remission (CR) rate after 1 course of induction, disease-free survival (DFS), and overall survival (OS) compared to those with ≤7% CD34 expression (p=0.0038; p=0.001; p<0.0001). A multivariate analysis revealed that CD34 expression is a prognostic factor that is independent of FlT3-ITD for relapse, DFS and OS. We established a novel prognostic model based on the CD34 and FLT3 status at diagnosis, which could facilitate the segregation of patients into three prognostically different subgroups. We demonstrate that CD34 expression on blasts is a novel, poor predictor independent of FlT3-ITD in NPM1-mutated patients and established a new prognostic model based on the CD34 and FLT3 status at diagnosis, which may facilitate immediate clinical utility for prognostic stratification and risk-adapted therapeutic choices.
为了探究 CD34 表达在核仁磷酸蛋白 1 突变型急性髓系白血病(NPM1m+AML)中的预后价值,我们回顾性分析了 71 例 NPM1m+AML 患者。根据 ROC 分析,CD34 表达>7%的患者在 1 个疗程诱导后完全缓解(CR)率、无病生存(DFS)率和总生存(OS)率均低于 CD34 表达≤7%的患者(p=0.0038;p=0.001;p<0.0001)。多因素分析显示,CD34 表达是独立于 FLT3-ITD 的复发、DFS 和 OS 的预后因素。我们基于诊断时的 CD34 和 FLT3 状态建立了一个新的预后模型,该模型可以将患者分为三个具有不同预后的亚组。我们证明,在 NPM1 突变型患者中,CD34 表达是一种独立于 FLT3-ITD 的新的不良预后预测指标,并建立了一个基于诊断时 CD34 和 FLT3 状态的新的预后模型,该模型可能有助于立即进行预后分层和风险适应的治疗选择。