Acute Myeloid Leukemia with Normal Cytogenetics and NPM1-Mutation: Impact of Mutation Topography on Outcomes

被引:1
作者
Zhao, Mingyue [1 ]
Liao, Mingyue [1 ]
Gale, Robert Peter [1 ,2 ]
Zhang, Meijie [3 ]
Wu, Lixin [1 ]
Yan, Nan [1 ]
Liu, Lixia [4 ]
Qin, Jiayue [4 ]
Cao, Shanbo [4 ]
Chang, Yingjun [1 ]
Jiang, Qian [1 ]
Xu, Lanping [1 ]
Zhang, Xiaohui [1 ]
Huang, Xiaojun [1 ,5 ]
Jiang, Hao [1 ]
Ruan, Guorui [1 ]
机构
[1] Peking Univ, Inst Hematol, Natl Clin Res Ctr Hematol Dis, Beijing Key Lab Hematopoiet Stem Cell Transplantat, Beijing 100044, Peoples R China
[2] Imperial Coll Sci Technol & Med, Ctr Haematol, Dept Immunol & Inflammat, London SW7 2AZ, England
[3] Med Coll Wisconsin, Div Biostat, IBMTR ABMTR, Milwaukee, WI 53226 USA
[4] Acornmed Biotechnol Co Ltd, Floor 18,Block 5,Yard 18,Kechuang 13 RD, Beijing 100176, Peoples R China
[5] Peking Univ, Acad Adv Interdisciplinary Studies, Peking Tsinghua Ctr Life Sci, Beijing 100091, Peoples R China
基金
中国国家自然科学基金;
关键词
acute myeloid leukemia; normal cytogenetics; NPM1; mutation; risk stratification; DNMT3A MUTATIONS; PROGNOSTIC IMPACT; YOUNGER ADULTS; NPM1; MUTATIONS; AML; CLASSIFICATION; TET2; MRD;
D O I
10.3390/biomedicines12122921
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: About half of adults with acute myeloid leukemia with normal cytogenetics (CN-AML) have NPM1 mutations. There is controversy regarding their prognosis and best therapy. Methods: We studied 150 subjects with these features using targeted regional sequencing. Prognostic stratification was carried out based on risk factors, and we assessed the effects of two post-remission strategies with and without transplant across risk cohorts. Results: In multi-variable analyses, a positive MRD test after the second consolidation cycle (HR = 6.00; 95% CI [3.31, 10.85]; p < 0.001), DNMT3A mutations (HR = 3.01 [1.57, 5.78]; p < 0.001), FLT3-ITD mutation with high variant allele frequency (HR = 4.40 [1.89, 10.24]; p < 0.001) and DDX11 mutations (HR = 4.38 [2.38, 8.04]; p < 0.001) were independently correlated with higher cumulative incidence of relapse (CIR) and worse leukemia-free survival (LFS) (HR = 5.49 [3.01, 10.04]; p < 0.001; HR = 2.99 [1.60, 5.62]; p < 0.001; HR = 4.20 [1.87, 9.40]; p < 0.001; and HR = 4.22, 95% CI [1.99, 8.95], p < 0.001). Subjects with >= 1 high-risk co-variate who received a transplant had a lower CIR and better LFS, whereas others did not. Conclusions: We identified co-variates associated with CIR and LFS in subjects of NPM1-mutated CN-AML.
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页数:11
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