Table 2.

Comparing baseline variables and outcomes for CP-CML patients receiving asciminib at 200 mg twice daily (phase 1 study) or dose-modified ponatinib (OPTIC)

Asciminib 200 mg twice daily18 Ponatinib 45 mg (OPTIC)13 Ponatinib 30 mg (OPTIC)13 Comments
No. of patients 52 94 94  
Follow-up 17 mo 32 mo 32 mo  
Molecular status at baseline BCR::ABL1IS
54%> 10%
25% 1-10%
15% <1% 
   
Prior ponatinib therapy 28/52 (54%) NA NA  
Results 
 Discontinued therapy 17/52 (33%) 44/94 (47%)
For all patients on 45 mg, not just T315I cohort 
53/95 (56%)
For all patients on 30 mg, not just T315I cohort 
Asciminib appears to be better tolerated 
 MMR rate at
 12 mo 
12/21 (57%) in ponatinib-naive cohort NA NA  
 MMR rate at 24 mo 14/21 (66%) in ponatinib-naive cohort NA NA  
     
 MR2 at 12 mo NA 15/25 (60%) 5/20 (25%)  
 MR2 at 24 mo NA    
 AOEs 2/52 (4%)
 
9/94 (9.6%) 5/94 (5.3%) AOE risk with asciminib may be similar to ponatinib 30 mg (OPTIC dosing) 
Asciminib 200 mg twice daily18 Ponatinib 45 mg (OPTIC)13 Ponatinib 30 mg (OPTIC)13 Comments
No. of patients 52 94 94  
Follow-up 17 mo 32 mo 32 mo  
Molecular status at baseline BCR::ABL1IS
54%> 10%
25% 1-10%
15% <1% 
   
Prior ponatinib therapy 28/52 (54%) NA NA  
Results 
 Discontinued therapy 17/52 (33%) 44/94 (47%)
For all patients on 45 mg, not just T315I cohort 
53/95 (56%)
For all patients on 30 mg, not just T315I cohort 
Asciminib appears to be better tolerated 
 MMR rate at
 12 mo 
12/21 (57%) in ponatinib-naive cohort NA NA  
 MMR rate at 24 mo 14/21 (66%) in ponatinib-naive cohort NA NA  
     
 MR2 at 12 mo NA 15/25 (60%) 5/20 (25%)  
 MR2 at 24 mo NA    
 AOEs 2/52 (4%)
 
9/94 (9.6%) 5/94 (5.3%) AOE risk with asciminib may be similar to ponatinib 30 mg (OPTIC dosing) 

Data reproduced with permission from Cortes et al,13  Hughes et al14 , and Cortes et al.18 

CCyR, complete cytogenetic response; CHR, complete hematologic response; NA, not available.

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