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. 2023 Jun 30;6(7):e1376. doi: 10.1002/hsr2.1376

Table 3.

Mutations with unknown effect on TKI therapy, choice of TKI, and molecular response observed.

Patient number Mutation detected TKI choice Molecular responsea
2 Q300* Imatinib Good
7 D363_R386del Nilotinib Poor
15 V260G Imatinib Undetermined/static
24 V304RfsTer14 Imatinib Undetermined
30 K219R Nilotinib Good
32 A412S Imatinib Good
44 E275Kb Nilotinib Poor
Dasatinib Good
70 G259D Imatinib Undetermined
81 A399T Nilotinib Good
89 I242V Imatinib Poor
91 A399T Imatinib Undetermined
93 I293N Imatinib Good
N331D Imatinib Good
94 V260M Nilotinib Good
E282V Nilotinib Good
96 V280M Imatinib Good
99 H396Y Imatinib Good
100 A399T Imatinib Poor
102 V339M Imatinib Undetermined
105 G254R Dasatinib Good
113 Y312C Nilotinib Good
142 R307N Imatinib Good
170 C330R Nilotinib Poor
195 L248Vc Dasatinib Undetermined
L248_L247del Dasatinib Undetermined
198 V225F Imatinib Good
199 P367Q Dasatinib Undetermined
204 A399T Nilotinib Good
205 V260Ad Nilotinib Poor

Abbreviation: TKI, tyrosine kinase inhibitor.

Predicted responses:

a

Molecular responses were assessed according to the current European LeukemiaNet and National Comprehensive Cancer Network defined response criteria—using the same response milestones as for first‐line treatment. 3 , 7

b

Imatinib—resistant, Nilotinib—sensitive, Dasatinib—unknown.

c

Imatinib—resistant, Nilotinib—sensitive, Dasatinib—unknown.

d

Imatinib—resistant, Nilotinib—unknown, Dasatinib—unknown.