Table 1

Type and frequency of BCR-ABL kinase domain mutations at the time of relapse

TK domain mutationNo. of patientsProportion of patients with a KD mutation, %Frequency by type, %
All mutations 21 80 n.a. 
    P-loop 
        G250E 24 — 
        Q252H — 
        Y253H* 10 62 
        E255K/V* 19 — 
    Others D276G — 
    Contact site 
        F311I — 
        T315I* 19 28.5 
        F317L — 
    Activation site L384M* 10 9.5 
Dual mutations — — — 
    E255K/T315I 4.7 9.5 
    Y253H/L384M 4.7 — 
Unmutated n.a. 21 
TK domain mutationNo. of patientsProportion of patients with a KD mutation, %Frequency by type, %
All mutations 21 80 n.a. 
    P-loop 
        G250E 24 — 
        Q252H — 
        Y253H* 10 62 
        E255K/V* 19 — 
    Others D276G — 
    Contact site 
        F311I — 
        T315I* 19 28.5 
        F317L — 
    Activation site L384M* 10 9.5 
Dual mutations — — — 
    E255K/T315I 4.7 9.5 
    Y253H/L384M 4.7 — 
Unmutated n.a. 21 

Leukemic-cell samples obtained at relapse were evaluated for the presence or absence (WT) of a BCR-ABL KD mutation by both D-HPLC and direct sequencing as described in “Patients and methods.” Only 2 patients harbored 2 mutations.

n.a. indicates not applicable; —, not available.

*

Including patient with dual mutation.

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