Table 2.

Clinical characteristics of AML overexpressing Wt-FLT3


UPN

Age, y

FAB

WBC count, × 109/L

FLT3 transcripts, copies/μg RNA

Karyotype

Gene mutations
UPN 112   69   M4   82.2   266 947   Normal   None  
UPN 185   32   M2   30.0   516 010   t(8; 21)   None  
UPN 187   43   M2   24.7   561 052   Normal   None  
UPN 23   64   M0   197.4   1 731 514   Normal   MLL-TD, N-RAS 
UPN 67
 
21
 
M1
 
56.1
 
2 322 706
 
Normal
 
None
 

UPN

Age, y

FAB

WBC count, × 109/L

FLT3 transcripts, copies/μg RNA

Karyotype

Gene mutations
UPN 112   69   M4   82.2   266 947   Normal   None  
UPN 185   32   M2   30.0   516 010   t(8; 21)   None  
UPN 187   43   M2   24.7   561 052   Normal   None  
UPN 23   64   M0   197.4   1 731 514   Normal   MLL-TD, N-RAS 
UPN 67
 
21
 
M1
 
56.1
 
2 322 706
 
Normal
 
None
 

There were 5 cases whose FLT3 transcript level was more than 200 000 copies/μg RNA in AML without FLT3/ITD. In particular, 2 cases, UPNs 23 and 67, revealed an extremely high level of the FLT3 transcript. The FLT3 products of these 2 cases were tyrosine phosphorylated, as shown in Figure 3C.

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