Table 4

Distribution of concurrent mutations in correlation to the functionally categorized FLT3-ITD groups

Concurrent mutations (%)
FLT3-ITD insertion site (%)
P
JMD (572-603)Hinge region (604-609)Beta1 of TKD1 (610-615)3′ of beta1 (616 and C-terminal)
NPM1 71/115 (62) 16/30 (53) 29/56 (52) 2/5 (40) .48 
MLL-PTD 7/112 (6) 4/28 (14) 5/55 (9) 0/5 .45 
CEBPA 6/101 (6) 2/25 (8) 2/49 (4) 0/5 .86 
FLT3-TKD 6/114 (5) 1/30 (3) 2/55 (4) 0/5 .999 
NRAS 7/106 (7) 0/23 2/47 (4) 0/5 .71 
Concurrent mutations (%)
FLT3-ITD insertion site (%)
P
JMD (572-603)Hinge region (604-609)Beta1 of TKD1 (610-615)3′ of beta1 (616 and C-terminal)
NPM1 71/115 (62) 16/30 (53) 29/56 (52) 2/5 (40) .48 
MLL-PTD 7/112 (6) 4/28 (14) 5/55 (9) 0/5 .45 
CEBPA 6/101 (6) 2/25 (8) 2/49 (4) 0/5 .86 
FLT3-TKD 6/114 (5) 1/30 (3) 2/55 (4) 0/5 .999 
NRAS 7/106 (7) 0/23 2/47 (4) 0/5 .71 

Patients with > 1 ITD were excluded.

JMD, juxtamembrane domain; TKD1, tyrosine kinase domain-1; NPM1, nucleophosmin 1; MLL-PTD, partial tandem duplications of the mixed lineage leukemia gene; CEBPA, CCAAT/enhancer binding protein alpha; FLT3-TKD, mutations in the tyrosine kinase domain of the FLT3 gene; and NRAS, neuroblastoma RAS viral oncogene homolog.

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