Department of Hematology, University Hospital Virgen del Rocío, Seville, Spain.
Department of Hematology, University Hospital Virgen del Rocío, Seville, Spain.
Clin Lymphoma Myeloma Leuk. 2018 Jul;18(7):469-474.e1. doi: 10.1016/j.clml.2018.05.004. Epub 2018 May 10.
The prognosis of patients with lower-risk myelodysplastic syndrome (LR-MDS) is very heterogeneous. In addition to survival estimates, identification of factors related to the probability of leukemic progression might help prognosis assessment.
The present study is a retrospective analysis of 409 patients with primary LR-MDS. The probability of leukemic progression was estimated in the competing risk framework by the cumulative incidence method considering death without acute myeloid leukemia (AML) as a competing event.
Sixty-six patients (16.1%) progressed to AML. The following covariates influenced the probability of leukemic progression in a multivariate competing risk regression model: intermediate karyotype versus diploid or chromosome 5 deletion, 5% to 9% bone marrow blast percentage, platelet count <50 × 10e/L and age younger than 75 years.
According to these, a predictive model is proposed, which categorizes patients with different probability of leukemic progression (P < .001). Validation of these results might help prognostic refinement of patients with LR-MDS.
低危骨髓增生异常综合征(LR-MDS)患者的预后差异很大。除了生存估计外,确定与白血病进展概率相关的因素可能有助于预后评估。
本研究对 409 例原发性 LR-MDS 患者进行了回顾性分析。采用累积发生率法,在竞争风险框架下估计白血病进展的概率,将非急性髓系白血病(AML)死亡视为竞争事件。
66 例患者(16.1%)进展为 AML。多变量竞争风险回归模型中的以下协变量影响白血病进展的概率:中数核型与二倍体或 5 号染色体缺失、骨髓原始细胞比例为 5%至 9%、血小板计数<50×10e/L 和年龄<75 岁。
据此提出了一个预测模型,可将白血病进展概率不同的患者进行分类(P<0.001)。验证这些结果可能有助于细化 LR-MDS 患者的预后。