Table 1

Characteristics of clinically classified IM responders and IM nonresponders

CharacteristicIM respondersIM nonrespondersP*
Quantitative features    
    WBC at diagnosis Range: [25.5, 450]; mean, 149; CI: [62.9, 235] Range: [32.2, 536] mean, 204; CI: [101, 252] .42 
    Age, y Range: [23,76]; mean, 52.64; CI: [49.47, 55.80] Range: [29,77]; mean, 55.71; CI: [53.86, 57.57] .60 
    Mutant BCR-ABL transcripts, percentage Range: [0, 20]; mean, 10.1; CI: [8.3, 12.2] Range: [9, 40]; mean, 24.5; CI: [21.5, 26.5] < .003 
    NA 1 (9.1%) 4 (28.6%)  
    No. of colonies as percentage of untreated cells CFC IM 1μM Range: [14.2, 53]; mean, 35.6; CI: [32.7, 38.4] Range: [40.6, 92] mean, 60.1; CI: [57.6, 62.6] < .001 
    CFC IM 5μM Range: [7.7, 42.6]; mean, 22.7; CI: [20.5, 24.9] Range: [34, 64]; mean, 48.66; CI: [47.4, 49.9] < .001 
    CFC IM 10μM Range: [6.6, 42]; mean, 22.3; CI: [20, 24.6] Range: [20.8, 61.3]; mean, 44.0; CI: [41.8, 46.1] < .001 
    Time from diagnosis to IM treatment, d Range: [7, 335]; mean, 60.36; CI: [-122, 242] Range: [7, 377]; mean, 107; CI: [-133, 347] .29 
Qualitative features    
    Sokal risk score   .928 
        Low 1 (14.3%); CI: NA§ 2 (9.1%); CI: [0.14, 1.22]  
        Intermediate 7 (42.9%); CI: [0.84, 0.94] 6 (63.6%); CI: [0.89, 0.96]  
        High 3 (35.7%); CI: [0.58, 2.9] 5 (27.3%); CI: [1.56, 2.55]  
        NA 1 (7.14%)  
    Sex   > .311 
        Male 6 (54.6%) 8 (57.1%)  
        Female 5 (45. 5%) 6 (42.9%)  
    Prior interferon   > .158 
        Yes 3 (21.4%)  
        No 11 (100%) 11 (78.6%)  
    Prior hydroxyurea   .072 
        Yes 7 (63.6%) 14 (100%)  
        No 4 (36.4%)  
    Daily IM dose   .161 
        400 mg 9 (81.8%) 8 (57.4%)  
        400-600 mg 2 (18.2%) 4 (28.6%)  
        400-800 mg 2 (14.3%)  
    Primary/secondary resistance   < .001 
        NA 11 (100%)  
        Primary resistance 9 (64.3%)  
        Secondary resistance 5 (35.7%)  
CharacteristicIM respondersIM nonrespondersP*
Quantitative features    
    WBC at diagnosis Range: [25.5, 450]; mean, 149; CI: [62.9, 235] Range: [32.2, 536] mean, 204; CI: [101, 252] .42 
    Age, y Range: [23,76]; mean, 52.64; CI: [49.47, 55.80] Range: [29,77]; mean, 55.71; CI: [53.86, 57.57] .60 
    Mutant BCR-ABL transcripts, percentage Range: [0, 20]; mean, 10.1; CI: [8.3, 12.2] Range: [9, 40]; mean, 24.5; CI: [21.5, 26.5] < .003 
    NA 1 (9.1%) 4 (28.6%)  
    No. of colonies as percentage of untreated cells CFC IM 1μM Range: [14.2, 53]; mean, 35.6; CI: [32.7, 38.4] Range: [40.6, 92] mean, 60.1; CI: [57.6, 62.6] < .001 
    CFC IM 5μM Range: [7.7, 42.6]; mean, 22.7; CI: [20.5, 24.9] Range: [34, 64]; mean, 48.66; CI: [47.4, 49.9] < .001 
    CFC IM 10μM Range: [6.6, 42]; mean, 22.3; CI: [20, 24.6] Range: [20.8, 61.3]; mean, 44.0; CI: [41.8, 46.1] < .001 
    Time from diagnosis to IM treatment, d Range: [7, 335]; mean, 60.36; CI: [-122, 242] Range: [7, 377]; mean, 107; CI: [-133, 347] .29 
Qualitative features    
    Sokal risk score   .928 
        Low 1 (14.3%); CI: NA§ 2 (9.1%); CI: [0.14, 1.22]  
        Intermediate 7 (42.9%); CI: [0.84, 0.94] 6 (63.6%); CI: [0.89, 0.96]  
        High 3 (35.7%); CI: [0.58, 2.9] 5 (27.3%); CI: [1.56, 2.55]  
        NA 1 (7.14%)  
    Sex   > .311 
        Male 6 (54.6%) 8 (57.1%)  
        Female 5 (45. 5%) 6 (42.9%)  
    Prior interferon   > .158 
        Yes 3 (21.4%)  
        No 11 (100%) 11 (78.6%)  
    Prior hydroxyurea   .072 
        Yes 7 (63.6%) 14 (100%)  
        No 4 (36.4%)  
    Daily IM dose   .161 
        400 mg 9 (81.8%) 8 (57.4%)  
        400-600 mg 2 (18.2%) 4 (28.6%)  
        400-800 mg 2 (14.3%)  
    Primary/secondary resistance   < .001 
        NA 11 (100%)  
        Primary resistance 9 (64.3%)  
        Secondary resistance 5 (35.7%)  

NA indicates not available.

*

P values were calculated using the Welch 2-sample t test at the 5% significant level under the null hypothesis H0: mean (IM responders) = mean (IM nonresponders).

P value of mutant BCR-ABL transcript frequency was calculated after all the missing values were taken out of the sample.

Kruskal-Wallis test was used to calculate P values of ordered categorical variable for Sokal risk score and daily IM dose.

§

CI for low IM responders in the low Sokal risk group is not available because there is only one patient in this category.

Fisher exact test was used to calculate P values of nonordered categorical variable for sex, prior interferon, and prior hydroxyurea.

Primary/secondary resistance is not available for all IM responders.

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