Table 3.

Mutation analysis and clinical outcome in patients with a greater than 2-fold rise in BCR-ABL according to the disease phase at the start of imatinib





Acquired resistance

Disease phase at the start of imatinib
More than 2-fold rise in BCR-ABL (%)
No. patients
AP or BC
Loss of CHR
Cytogenetic relapse
No acquired resistance
Blast crisis, n = 5  3 (60)       
   Mutation    1   1   —   —   —  
   No mutation    2   2   —   —   —  
Accelerated phase, n = 27  15 (56)       
   Mutation    12   6   2   4   —  
   No mutation    3   1   —   1   1  
Late chronic phase, n = 48  18 (38)       
   Mutation    11   6   2   1   2  
   No mutation    7   2   —   2   3  
Early chronic phase, n = 134  20 (15)       
   Mutation    10   3   3   3   1  
   No mutation
 

 
10
 
1
 

 
4
 
5
 




Acquired resistance

Disease phase at the start of imatinib
More than 2-fold rise in BCR-ABL (%)
No. patients
AP or BC
Loss of CHR
Cytogenetic relapse
No acquired resistance
Blast crisis, n = 5  3 (60)       
   Mutation    1   1   —   —   —  
   No mutation    2   2   —   —   —  
Accelerated phase, n = 27  15 (56)       
   Mutation    12   6   2   4   —  
   No mutation    3   1   —   1   1  
Late chronic phase, n = 48  18 (38)       
   Mutation    11   6   2   1   2  
   No mutation    7   2   —   2   3  
Early chronic phase, n = 134  20 (15)       
   Mutation    10   3   3   3   1  
   No mutation
 

 
10
 
1
 

 
4
 
5
 

Late chronic phase indicates patients who commenced imatinib 12 months or more after diagnosis. Early chronic phase indicates patients who commenced imatinib less than 12 months after diagnosis. Dashes indicate that there were no patients in the category.

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