Table 2

Mutations identified during treatment

Nilotinib 300 mg twice daily (n = 282), nNilotinib 400 mg twice daily (n = 281), nImatinib 400 mg once daily (n = 283), n
Patients with ≥1 postbaseline mutational analysis* 228 215 237 
Patients with mutations 11 11 21 
New mutations by Sokal score    
 Low 
 Intermediate 
 High 12 
Mutation category    
 T315I 
 Less sensitive to nilotinib 
 Other mutations 2§ 14 
 Multiple mutations 
Mutations||    
 M244V 
 G250E 
 Q252H 
 Y253H 
 E255K 
 E255V 
 D276G 
 T315I 
 M351T 
 E355G 
 F359C 
 F359I 
 F359V 
 H396R 
 E450G 
 E459K 
Nilotinib 300 mg twice daily (n = 282), nNilotinib 400 mg twice daily (n = 281), nImatinib 400 mg once daily (n = 283), n
Patients with ≥1 postbaseline mutational analysis* 228 215 237 
Patients with mutations 11 11 21 
New mutations by Sokal score    
 Low 
 Intermediate 
 High 12 
Mutation category    
 T315I 
 Less sensitive to nilotinib 
 Other mutations 2§ 14 
 Multiple mutations 
Mutations||    
 M244V 
 G250E 
 Q252H 
 Y253H 
 E255K 
 E255V 
 D276G 
 T315I 
 M351T 
 E355G 
 F359C 
 F359I 
 F359V 
 H396R 
 E450G 
 E459K 
*

Triggers for postbaseline mutational analysis included mutations or polymorphisms at baseline, lack of response or loss of response on treatment, and end of treatment.

Mutations less sensitive to nilotinib are E255K/V, F359C/V, and Y253H.

Includes imatinib-resistant, nilotinib-sensitive mutations (ie, all mutations except E255K/V, F359C/V, Y253H, and T315I).

§

Of the 2 nilotinib-treated patients with other mutations, one had an E459K mutation and the other had a G250E mutation.

||

Individual mutation totals include patients with multiple mutations.

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