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世界卫生组织定义的非典型慢性髓性白血病的靶向二代测序及危险因素鉴定

Targeted next generation sequencing and identification of risk factors in World Health Organization defined atypical chronic myeloid leukemia.

作者信息

Patnaik Mrinal M, Barraco Daniela, Lasho Terra L, Finke Christy M, Reichard Kaaren, Hoversten Katherine P, Ketterling Rhett P, Gangat Naseema, Tefferi Ayalew

机构信息

Division of Hematology, Mayo Clinic, Rochester, Minnesota, USA.

Hematology, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

Am J Hematol. 2017 Jun;92(6):542-548. doi: 10.1002/ajh.24722. Epub 2017 Apr 29.

Abstract

Atypical chronic myeloid leukemia (aCML) is an aggressive myeloid neoplasm with overlapping features of myelodysplastic syndromes (prominent granulocytic dysplasia) and myeloproliferative neoplasms (neutrophilic leukocytosis). We studied 25 molecularly-annotated and World Health Organization defined aCML patients; median age 70 years, 84% males. Cytogenetic abnormalities were seen in 36% and gene mutations in 100%. Mutational frequencies were, ASXL1 28%, TET2 16%, NRAS 16%, SETBP1 12%, RUNX1 12%, ETNK1 8%, and PTPN11 4%. Fifteen patients (60%) had >1 mutation, while 9 (36%) had ≥3. The median overall survival (OS) was 10.8 months and at last follow up (median 11 months), 17 (68%) deaths and 2 (8%) leukemic transformations were documented. On univariate analysis, survival was adversely impacted by advanced age (P = .02), low hemoglobin (P = .01), red blood cell transfusion dependence (P = .03), high white blood cell count (P = .02), TET2 (P = .03), NRAS (P = .04), PTPN11 (P = .02) mutations and the presence of ≥3 gene mutations (P = .006); ASXL1, SETBP1, and ETNK1 mutations did not impact OS. In multivariable analysis, advanced age (P = .003) [age >67: HR 10.1, 95% CI 1.3-119], low hemoglobin (P = .008) [HB< 10 gm/dL: HR 8.2, 95% CI 1.6-23.2] and TET2 mutations (P = .01) [HR 8.8, 95% CI 1.6-47.7] retained prognostic significance. We then used age >67 years, hemoglobin <10 gm/dL and the presence of TET2 mutations (each counted as one risk factor) to create a hazard ratio weighted prognostic model; effectively stratifying patients into two risk categories, low (0-1 risk factor) and high (≥2 risk factors), with median OS of 18 and 7 months, respectively.

摘要

非典型慢性髓系白血病(aCML)是一种侵袭性髓系肿瘤,具有骨髓增生异常综合征(显著的粒细胞发育异常)和骨髓增殖性肿瘤(中性粒细胞增多)的重叠特征。我们研究了25例经分子注释且符合世界卫生组织定义的aCML患者;中位年龄70岁,男性占84%。36%的患者存在细胞遗传学异常,100%的患者存在基因突变。突变频率分别为:ASXL1 28%、TET2 16%、NRAS 16%、SETBP1 12%、RUNX1 12%、ETNK1 8%和PTPN11 4%。15例患者(60%)有>1种突变,而9例(36%)有≥3种突变。中位总生存期(OS)为10.8个月,在最后一次随访时(中位随访11个月),记录到17例(68%)死亡和2例(8%)白血病转化。单因素分析显示,高龄(P = 0.02)、低血红蛋白(P = 0.01)、依赖红细胞输血(P = 0.03)、高白细胞计数(P = 0.02)、TET2(P = 0.03)、NRAS(P = 0.04)、PTPN11(P = 0.02)突变以及存在≥3种基因突变(P = 0.006)对生存有不利影响;ASXL1、SETBP1和ETNK1突变不影响总生存期。多因素分析显示,高龄(P = 0.003)[年龄>67岁:HR 10.1,95%CI 1.3 - 119]、低血红蛋白(P = 0.008)[血红蛋白<10 g/dL:HR 8.2,95%CI 1.6 - 23.2]和TET2突变(P = 0.01)[HR 8.8,95%CI 1.6 - 47.7]保留了预后意义。然后,我们使用年龄>67岁、血红蛋白<10 g/dL和存在TET2突变(每项计为一个危险因素)来创建一个风险比加权预后模型;有效地将患者分为两个风险类别,低风险(0 - 1个危险因素)和高风险(≥2个危险因素),中位总生存期分别为18个月和7个月。

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