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作 者:崔亚娟 江倩[2] 刘晋琴 李冰 徐泽锋 秦铁军 张悦 蔡文宇 张宏丽 方力维 潘丽娟 胡耐博 曲士强 肖志坚
机构地区:[1]中国医学科学院、北京协和医学院血液学研究所、血液病医院,实验血液学国家重点实验室,天津300020 [2]北京大学人民医院
出 处:《中华血液学杂志》2017年第1期28-32,共5页Chinese Journal of Hematology
基 金:国家自然科学基金(81530008、81370611、81270585、81470297);北京协和学者创新研究团队
摘 要:目的探讨慢性中性粒细胞白血病(CNL)患者的临床表现、细胞遗传学和基因突变等实验室特征及预后因素。 方法对符合2016年WHO诊断分型标准的16例CNL患者进行资料采集,随访患者并进行预后分析。利用直接测序法检测CSF3R、ASXL1、SETBP1、CALR、MPL基因突变状态,对有突变的样本进行克隆后测序鉴定,采用等位基因特异性聚合酶链反应(AS-PCR)检测JAK2 V617F突变。 结果16例CNL患者中位发病年龄为64(43~80)岁,男性占75%(12/16),确诊时中位HGB水平为114(81~154)g/L,中位WBC为41.20(26.05~167.70)×109/L,中位PLT为238(91~394)×109/L。中位骨髓纤维化水平为1(0~3)级。除1例t(1;7)(p32;q11)、1例+21克隆异常及1例14ps+外,余患者均为正常核型。16例CNL患者中,CSF3R T618I突变检出率为100%(16/16),ASXL1突变检出率为81%(13/16),SETBP1突变检出率为63%(10/16),1例患者携带CALR K385fs*47突变,所有患者均无JAK2 V617F突变及MPL突变。CNL患者中位生存期为24(95%CI 18~30)个月。初诊WBC≥50×109/L者中位生存期较〈50×109/L者短(11个月对39个月,P=0.005)。 结论CSF3R T618I突变是CNL的特异性突变。CNL患者中位生存期24个月,确诊时WBC≥50×109/L是不良预后因素。Objective To investigate the clinical manifestation, cytogenetics, gene mutations and prognostic factors of chronic neutrophilic leukemia (CNL). Methods 16 CNL cases, according to WHO (2016)-definition, were reviewed retrospectively. Identifications of the CSF3R, ASXL1, SETBP1, CALR and MPL mutations were performed by direct sequencing. JAK2 V617F mutation was detected by AS- PCR. Results Of the 16 CNL patients, the median age was 64(43-80) years with a male predominance of 75% ( 12/16 ). The median hemoglobin was 114 ( 81-154 ) g/L, with median WBC of 41.20 (26.05-167.70 ) ( 10VL and median PLT of 238 (91-394)× 109/L.The median level of marrow fibrosis (MF) was 1 (0-3) degree. There was no other cytogenetic abnormalities except t(1;7) (p32;q11 ), +21 and 14ps+ for each. All the 16 CNL patients harbored CSF3R T618I mutation. ASXL 1 mutations were identified in 81% (13/16), while SETBP1 mutations were confirmed in 63% (10/16). The CALR K385fs*47 mutation was found. There was no mutation in JAK2 V617F or MPL in the above 16 patients. The median overall survival (OS) of patients presented with WBC≥50 × 109/L at diagnosis (11 months) was significantly shorter than of WBC 〈 50× 109/L (39 months, P=0.005). Conclusion CSF3R T618I mutation was specific for CNL. The median OS of CNL patients was 24 months, and WBC〉50 × 109/L at diagnosis was an unfavorable prognostic factor.
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