Acute Myeloid Leukemia (AML) with Erythroid Predominance Exhibits Clinical and Molecular Characteristics that Differ from Other Types of AML

被引:24
作者
Zuo, Zhuang [1 ]
Medeiros, L. Jeffrey [1 ]
Chen, Zhao [1 ]
Liu, Dingsheng [1 ]
Bueso-Ramos, Carlos E. [1 ]
Luthra, Rajyalakshmi [1 ]
Wang, Sa A. [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Hematopathol, Houston, TX 77030 USA
关键词
WORLD-HEALTH-ORGANIZATION; MYELODYSPLASTIC SYNDROMES; ACUTE ERYTHROLEUKEMIA; NPM1; MUTATIONS; JAK2; V617F; CLASSIFICATION; RARE; CRITERIA; GATA1;
D O I
10.1371/journal.pone.0041485
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The clinical importance of erythroid predominance in bone marrow of patients with acute myeloid leukemia (AML) is controversial. These cases represent a heterogeneous group of diseases that historically have been classified into different categories. We studied 313 AML patients and specifically compared the clinical, cytogenetic, and molecular features of cases of AML with erythroid predominance, arbitrarily defined as >= 50% erythroid precursors, to AML cases without erythroid predominance. We also assessed 51 patients with a high-grade myelodysplastic syndrome (MDS), refractory anemia with excess blasts (RAEB). All neoplasms were classified according to the World Health Organization classification. With the exception of therapy-related AML/MDS, the presence of erythroid predominance in variously classified categories of AML was associated with a survival advantage. In addition, AML with erythroid predominance had a lower frequency of cytogenetic abnormalities as well as a lower frequency of mutations involving NPM1, NRAS and FLT3 as compared with AML without erythroid predominance. We conclude that the clinical, cytogenetic, and molecular features of AML with erythroid predominance in the non-therapy-related setting are much closer to those of a high-grade myelodysplastic syndrome than they are to other types of AML.
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相关论文
共 27 条
[1]   A comparative study of molecular mutations in 381 patients with myelodysplastic syndrome and in 4130 patients with acute myeloid leukemia [J].
Bacher, Ulrike ;
Haferlach, Torsten ;
Kern, Wolfgang ;
Haferlach, Claudia ;
Schnittger, Susanne .
HAEMATOLOGICA, 2007, 92 (06) :744-752
[2]   Comparison of genetic and clinical aspects in patients with acute myeloid leukemia and myelodysplastic syndromes all with more than 50% of bone marrow erythropoietic cells [J].
Bacher, Ulrike ;
Haferlach, Claudia ;
Alpermann, Tamara ;
Kern, Wolfgang ;
Schnittger, Susanne ;
Haferlach, Torsten .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2011, 96 (09) :1284-1292
[3]   FLT3 and NPM1 Mutations in Myelodysplastic Syndromes Frequency and Potential Value for Predicting Progression to Acute Myeloid Leukemia [J].
Bains, Ashish ;
Luthra, Rajyalakshmi ;
Medeiros, L. Jeffrey ;
Zuo, Zhuang .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 2011, 135 (01) :62-69
[4]   PROPOSED REVISED CRITERIA FOR THE CLASSIFICATION OF ACUTE MYELOID-LEUKEMIA - A REPORT OF THE FRENCH-AMERICAN-BRITISH COOPERATIVE GROUP [J].
BENNETT, JM ;
CATOVSKY, D ;
DANIEL, MT ;
FLANDRIN, G ;
GALTON, DAG ;
GRALNICK, HR ;
SULTAN, C .
ANNALS OF INTERNAL MEDICINE, 1985, 103 (04) :620-625
[5]  
Di Guglielmo G., 1917, FOLIA MED, V3, P386
[6]   Mutant nucleophosmin (NPM1) predicts favorable prognosis in younger adults with acute myeloid leukemia and normal cytogenetics:: interaction with other gene mutations [J].
Döhner, K ;
Schlenk, RF ;
Habdank, M ;
Scholl, C ;
Rücker, FG ;
Corbacioglu, A ;
Bullinger, L ;
Fröhling, S ;
Döhner, H .
BLOOD, 2005, 106 (12) :3740-3746
[7]   Genetic deletions in AML and MDS [J].
Ebert, Benjamin L. .
BEST PRACTICE & RESEARCH CLINICAL HAEMATOLOGY, 2010, 23 (04) :457-461
[8]   Rare occurrence of the JAK2 V617F mutation in AML subtypes M5, M6, and M7 [J].
Fröhling, S ;
Lipka, DB ;
Kayser, S ;
Scholl, C ;
Schlenk, RF ;
Döhner, H ;
Gilliland, DG ;
Levine, RL ;
Döhner, K .
BLOOD, 2006, 107 (03) :1242-1243
[9]  
Galton DAGDJ, 1975, BR J HAEMATOL, P31
[10]   Refinement of cytogenetic classification in acute myeloid leukemia: determination of prognostic significance of rare recurring chromosomal abnormalities among 5876 younger adult patients treated in the United Kingdom Medical Research Council trials [J].
Grimwade, David ;
Hills, Robert K. ;
Moorman, Anthony V. ;
Walker, Helen ;
Chatters, Stephen ;
Goldstone, Anthony H. ;
Wheatley, Keith ;
Harrison, Christine J. ;
Burnett, Alan K. .
BLOOD, 2010, 116 (03) :354-365