Table 3.

Reasons for ending protocol treatment




High-dose IFN

Low-dose IFN
Overall, n (%)  171 of 201 (85)   154 of 206 (75)  
IFN-related adverse reactions   76 (44)   45 (29)  
CML-related (acceleration or blast crisis)   40 (23)   48 (31)  
Stem cell transplantation   12 (7)   20 (13)  
Indication for imatinib   23 (13)   16 (10)  
Intercurrent other diseases   7 (4)   6 (4)  
Refusal, violation, other   6 (4)   12 (8)  
Unknown   7 (4)   7 (5)  
Over the first year, n (%)  73   59  
IFN-related adverse reactions   43 (59)   20 (34)  
CML-related   15 (21)   21 (36)  
Stem cell transplantation   7 (10)   8 (14)  
Indication for imatinib   2 (3)   2 (3)  
Intercurrent other diseases   3 (4)   3 (5)  
Refusal, violation, other   0 (0)   3 (5)  
Unknown
 
3 (4)
 
2 (3)
 



High-dose IFN

Low-dose IFN
Overall, n (%)  171 of 201 (85)   154 of 206 (75)  
IFN-related adverse reactions   76 (44)   45 (29)  
CML-related (acceleration or blast crisis)   40 (23)   48 (31)  
Stem cell transplantation   12 (7)   20 (13)  
Indication for imatinib   23 (13)   16 (10)  
Intercurrent other diseases   7 (4)   6 (4)  
Refusal, violation, other   6 (4)   12 (8)  
Unknown   7 (4)   7 (5)  
Over the first year, n (%)  73   59  
IFN-related adverse reactions   43 (59)   20 (34)  
CML-related   15 (21)   21 (36)  
Stem cell transplantation   7 (10)   8 (14)  
Indication for imatinib   2 (3)   2 (3)  
Intercurrent other diseases   3 (4)   3 (5)  
Refusal, violation, other   0 (0)   3 (5)  
Unknown
 
3 (4)
 
2 (3)
 
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