Table 1.

Cytogenetic abnormalities in V617F+ and V617F patients with MPDs




V617F+

V617F

P
Del(20q) total  28   1   < .001  
   PV   12   0   
   ET   5   0   
   IMF   10   1   
   MPD/MDS   1   0   
Del(13q) total  3   9   .17  
   ET   1   0   
   IMF   2   9   
Translocations total  2   8   .12  
   ET   0   4   
   IMF   2   4   
Trisomy 9  10   0   .01  
   PV   3   0   
   ET   3   0   
   IMF   4   0   
Trisomy 8  6   1   .23  
   PV   2   0   
   ET   2   0   
   IMF
 
2
 
1
 

 



V617F+

V617F

P
Del(20q) total  28   1   < .001  
   PV   12   0   
   ET   5   0   
   IMF   10   1   
   MPD/MDS   1   0   
Del(13q) total  3   9   .17  
   ET   1   0   
   IMF   2   9   
Translocations total  2   8   .12  
   ET   0   4   
   IMF   2   4   
Trisomy 9  10   0   .01  
   PV   3   0   
   ET   3   0   
   IMF   4   0   
Trisomy 8  6   1   .23  
   PV   2   0   
   ET   2   0   
   IMF
 
2
 
1
 

 

Data are pooled from several sources, including 3 prospective ET trials (599 patients with cytogenetic results)11,12 , the European Myelofibrosis Network (71 patients)17 , the Addenbrooke MPD clinic (89 patients), and previous collaborative studies 20q and 13q deletions in MPDs21 

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