Table 1

Patient characteristics at the time of starting 2G-TKI and 2.5-year probabilities of EFS, PFS, and OS*

VariablenEFS, %PFS, %Survival, %
Age, y  P = .84 P = .86 P = .77 
    > 55 40 84.5 87.6 91.8 
    ≤ 55 35 87.2 89.9 89.2 
Sex  P = .13 P = .11 P = .37 
    Male 35 80.6 82.7 88.4 
    Female 40 91.5 94.8 92.6 
Sokal risk group  P = .65 P = .77 P = .28 
    Low 15 92.3 92.3 100 
    Intermediate 29 82.2 85.9 83.2 
    High 31 86.4 89.8 93.5 
Status at the onset of imatinib therapy  P = .8 P = .94 P = .48 
    Newly diagnosed CP patients 28 85.1 89.1 86.1 
    Late CP 47 86.7 89.0 93.2 
Additional cytogenetic abnormalities at start of 2G-TKI  P = .17 P = .44 P = .25 
    No 63 88.3 90.0 92.5 
    Yes 12 74.1 83.3 81.5 
Percentage of Ph-positive marrow metaphases at start of 2G-TKI  P = .064 P = .14 P = .29 
    < 95% 28 96.4 95.2 96.4 
    ≥ 95% 47 79.9 84.5 87.9 
Time from imatinib failure to starting 2G-TKI  P = .42 P = .60 P = .84 
    ≤ 6 months 15 93.3 93.3 90.9 
    > 6 months 60 84.2 87.8 90.5 
Best cytogenetic response on imatinib  P = .002 P = .043 P = .017 
    0%-94% Ph+ 42 63.7 76.5 75.3 
    ≥ 95% Ph+ 33 92.6 92.6 96.4 
Hematologic resistance to imatinib  P = .29 P = .44 P = .78 
    Yes 55 79.7 90.3 89.5 
    No 20 88.3 85.0 91.4 
Maximal dose of imatinib  P = .55 P = .68 P = .82 
    400 mg/day 16 93.8 93.8 93.8 
    600 mg/day 29 81.5 85.4 87.9 
    800 mg/day 30 86.2 89.8 92.0 
KD mutation at start of 2G-TKI  P = .51 P = .31 P = .11 
    No 55 84.9 86.9 100 
    Yes 20 90.0 95.0 86.7 
Transcript type  P = .57 P = .62 P = .72 
    e14a2 26 83.9 83.9 86.3 
    e13a2 34 91.1 91.1 93.2 
    e14a2 and e13a2 15 78.3 93.3 93.3 
EVI-1 at start of 2G-TKI  P = .0001 P < .0001 P = .0003 
    Negative 67 90.6 93.8 95.2 
    Positive 43.7 43.7 47.5 
Percentage of blasts in bone marrow at start of 2G-TKI  P = .02 P = .1 P = .3 
    ≤ 5% 54 90.4 88.4 90.4 
    > 5% 21 66.7 77.1 83.8 
Hemoglobin level at start of 2G-TKI  P = .3 P = .5 P = .5 
    Normal 41 92.8 92.9 96.4 
    Low 34 82.3 86.7 89.6 
VariablenEFS, %PFS, %Survival, %
Age, y  P = .84 P = .86 P = .77 
    > 55 40 84.5 87.6 91.8 
    ≤ 55 35 87.2 89.9 89.2 
Sex  P = .13 P = .11 P = .37 
    Male 35 80.6 82.7 88.4 
    Female 40 91.5 94.8 92.6 
Sokal risk group  P = .65 P = .77 P = .28 
    Low 15 92.3 92.3 100 
    Intermediate 29 82.2 85.9 83.2 
    High 31 86.4 89.8 93.5 
Status at the onset of imatinib therapy  P = .8 P = .94 P = .48 
    Newly diagnosed CP patients 28 85.1 89.1 86.1 
    Late CP 47 86.7 89.0 93.2 
Additional cytogenetic abnormalities at start of 2G-TKI  P = .17 P = .44 P = .25 
    No 63 88.3 90.0 92.5 
    Yes 12 74.1 83.3 81.5 
Percentage of Ph-positive marrow metaphases at start of 2G-TKI  P = .064 P = .14 P = .29 
    < 95% 28 96.4 95.2 96.4 
    ≥ 95% 47 79.9 84.5 87.9 
Time from imatinib failure to starting 2G-TKI  P = .42 P = .60 P = .84 
    ≤ 6 months 15 93.3 93.3 90.9 
    > 6 months 60 84.2 87.8 90.5 
Best cytogenetic response on imatinib  P = .002 P = .043 P = .017 
    0%-94% Ph+ 42 63.7 76.5 75.3 
    ≥ 95% Ph+ 33 92.6 92.6 96.4 
Hematologic resistance to imatinib  P = .29 P = .44 P = .78 
    Yes 55 79.7 90.3 89.5 
    No 20 88.3 85.0 91.4 
Maximal dose of imatinib  P = .55 P = .68 P = .82 
    400 mg/day 16 93.8 93.8 93.8 
    600 mg/day 29 81.5 85.4 87.9 
    800 mg/day 30 86.2 89.8 92.0 
KD mutation at start of 2G-TKI  P = .51 P = .31 P = .11 
    No 55 84.9 86.9 100 
    Yes 20 90.0 95.0 86.7 
Transcript type  P = .57 P = .62 P = .72 
    e14a2 26 83.9 83.9 86.3 
    e13a2 34 91.1 91.1 93.2 
    e14a2 and e13a2 15 78.3 93.3 93.3 
EVI-1 at start of 2G-TKI  P = .0001 P < .0001 P = .0003 
    Negative 67 90.6 93.8 95.2 
    Positive 43.7 43.7 47.5 
Percentage of blasts in bone marrow at start of 2G-TKI  P = .02 P = .1 P = .3 
    ≤ 5% 54 90.4 88.4 90.4 
    > 5% 21 66.7 77.1 83.8 
Hemoglobin level at start of 2G-TKI  P = .3 P = .5 P = .5 
    Normal 41 92.8 92.9 96.4 
    Low 34 82.3 86.7 89.6 

P values were calculated using the log-rank method. Variables with a P value < .1 were included in the multivariate analysis for each outcome.

*

Other peripheral blood and bone marrow parameters are not included in the table, but they did not significantly predict for any of the outcomes.

Normal values are > 12.5 for males and > 11.5 for females.

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