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1306 例原发性骨髓纤维化患者的白血病转化:危险因素和预测模型的建立。

Leukemic transformation among 1306 patients with primary myelofibrosis: risk factors and development of a predictive model.

机构信息

Departments of Divisions of Hematology, Mayo Clinic, Rochester, MN, USA.

Departments of Hematopathology, Mayo Clinic, Rochester, MN, USA.

出版信息

Blood Cancer J. 2019 Jan 25;9(2):12. doi: 10.1038/s41408-019-0175-y.

Abstract

Among 1306 patients with primary myelofibrosis (PMF), we sought to identify risk factors that predicted leukemic transformation (LT) in the first 5 years of disease and also over the course of the disease. 149 (11%) LT were documented; patients who subsequently developed LT (n = 149), compared to those who remained in chronic phase disease (n = 1,157), were more likely to be males (p = 0.02) and display higher circulating blasts (p = 0.03), ASXL1 (p = 0.01), SRSF2 (p = 0.001) and IDH1 (p = 0.02) mutations. Logistic regression analysis identified IDH1, ASXL1 and SRSF2 mutations, very high-risk karyotype, age > 70 years, male sex, circulating blasts ≥ 3%, presence of moderate or severe anemia and constitutional symptoms, as predictors of LT in the first 5 years of diagnosis. Time-to-event Cox analysis confirmed LT prediction for IDH1 mutation (HR 4.3), circulating blasts ≥ 3% (HR 3.3), SRSF2 mutation (HR 3.0), age > 70 years (HR 2.1), ASXL1 mutation (HR 2.0) and presence of moderate or severe anemia (HR 1.9). HR-based risk point allocation resulted in a three-tiered LT risk model: high-risk (LT incidence 57%; HR 39.3, 95% CI 10.8-114), intermediate-risk (LT incidence 17%; HR 4.1, 95% CI 2.4-7.3) and low-risk (LT incidence 8%). The current study provides a highly discriminating LT predictive model for PMF.

摘要

在 1306 例原发性骨髓纤维化(PMF)患者中,我们试图确定预测疾病前 5 年内和整个疾病过程中白血病转化(LT)的风险因素。记录到 149 例(11%)LT;与仍处于慢性期疾病的患者(n=1157)相比,随后发生 LT(n=149)的患者更可能为男性(p=0.02)且循环中原始细胞比例更高(p=0.03)、ASXL1(p=0.01)、SRSF2(p=0.001)和 IDH1(p=0.02)突变更多。逻辑回归分析确定 IDH1、ASXL1 和 SRSF2 突变、极高危核型、年龄>70 岁、男性、循环中原始细胞比例≥3%、存在中重度贫血和全身症状是诊断后前 5 年内 LT 的预测因素。时间事件 Cox 分析证实 IDH1 突变(HR 4.3)、循环中原始细胞比例≥3%(HR 3.3)、SRSF2 突变(HR 3.0)、年龄>70 岁(HR 2.1)、ASXL1 突变(HR 2.0)和中重度贫血存在(HR 1.9)预测 LT。基于 HR 的风险点分配产生了一个三级 LT 风险模型:高危(LT 发生率 57%;HR 39.3,95%CI 10.8-114)、中危(LT 发生率 17%;HR 4.1,95%CI 2.4-7.3)和低危(LT 发生率 8%)。本研究为 PMF 提供了一个高度区分 LT 的预测模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/503a/6347609/7d28d520cd9a/41408_2019_175_Fig1_HTML.jpg

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