Table 3

Characteristics of clinically classified IM nonresponders with primary and secondary resistance

CharacteristicsPrimary resistanceSecondary resistanceP*
Quantitative features    
    WBC at diagnosis Range: [32.2, 536]; mean, 195; CI: [39.8, 350] Range: [122, 480] mean, 221; CI: [36.7, 406] .79 
    Age, y Range: [43, 77]; mean, 58; CI: [49.6, 66.4] Range: [29,66]; mean, 51.6; CI: [34.2, 69.0] .41 
    Mutant BCR-ABL transcripts, percentage Range: [18, 35]; mean, 25.8; CI: [13.5, 38.0] Range: [9, 40]; mean, 22.6; CI: [8.48, 36.7] .64 
    NA 4 (28.6%)  
    No. of colonies as percentage of untreated cells CFC IM 1μM Range: [41.1, 67]; mean, 54.1; CI: [47.1, 61.1] Range: [40.6, 92] mean=70.9; CI: [44.3, 97.4] .16 
    CFC IM 5μM Range: [36, 56.6]; mean, 47.7; CI: [43.0, 52.5] Range: [34, 64]; mean, 50.3; CI: [36.0, 64.7] .66 
    CFC IM 10μM Range: [29.1, 61.3]; mean, 44.1; CI: [34.9, 53.3] Range: [20.8, 60.3]; mean, 43.8; CI: [21.0, 66.5] .97 
    Time from diagnosis to IM treatment, d Range: [7, 302]; mean, 127.4; CI: [12.0, 178.5] Range: [13, 377]; mean, 127; CI: [-66.7, 321] .70 
Qualitative features    
    Sokal risk score   .434 
        High 5 (55.6%)  
        Intermediate 3 (33.3%) 3 (60%)  
        Low 1 (11.1%) 1 (20%)  
        NA 1 (20%)  
    Sex   .21§ 
        Female 5 (55.6%) 1 (20%)  
        Male 4 (44.5%) 4 (80%)  
    Prior interferon   .247§ 
        No 8 (88.9) 3 (60%)  
        Yes 1 (11.1%) 2 (40%)  
    Prior hydroxyurea   1§ 
        No 9 (100%) 5 (100%)  
        Yes  
    Daily IM dose   .177 
        400 mg 6 (66.7%) 2 (40%)  
        400-600 mg 3 (33.3%) 1 (20%)  
        400-800 mg 2 (40%)  
CharacteristicsPrimary resistanceSecondary resistanceP*
Quantitative features    
    WBC at diagnosis Range: [32.2, 536]; mean, 195; CI: [39.8, 350] Range: [122, 480] mean, 221; CI: [36.7, 406] .79 
    Age, y Range: [43, 77]; mean, 58; CI: [49.6, 66.4] Range: [29,66]; mean, 51.6; CI: [34.2, 69.0] .41 
    Mutant BCR-ABL transcripts, percentage Range: [18, 35]; mean, 25.8; CI: [13.5, 38.0] Range: [9, 40]; mean, 22.6; CI: [8.48, 36.7] .64 
    NA 4 (28.6%)  
    No. of colonies as percentage of untreated cells CFC IM 1μM Range: [41.1, 67]; mean, 54.1; CI: [47.1, 61.1] Range: [40.6, 92] mean=70.9; CI: [44.3, 97.4] .16 
    CFC IM 5μM Range: [36, 56.6]; mean, 47.7; CI: [43.0, 52.5] Range: [34, 64]; mean, 50.3; CI: [36.0, 64.7] .66 
    CFC IM 10μM Range: [29.1, 61.3]; mean, 44.1; CI: [34.9, 53.3] Range: [20.8, 60.3]; mean, 43.8; CI: [21.0, 66.5] .97 
    Time from diagnosis to IM treatment, d Range: [7, 302]; mean, 127.4; CI: [12.0, 178.5] Range: [13, 377]; mean, 127; CI: [-66.7, 321] .70 
Qualitative features    
    Sokal risk score   .434 
        High 5 (55.6%)  
        Intermediate 3 (33.3%) 3 (60%)  
        Low 1 (11.1%) 1 (20%)  
        NA 1 (20%)  
    Sex   .21§ 
        Female 5 (55.6%) 1 (20%)  
        Male 4 (44.5%) 4 (80%)  
    Prior interferon   .247§ 
        No 8 (88.9) 3 (60%)  
        Yes 1 (11.1%) 2 (40%)  
    Prior hydroxyurea   1§ 
        No 9 (100%) 5 (100%)  
        Yes  
    Daily IM dose   .177 
        400 mg 6 (66.7%) 2 (40%)  
        400-600 mg 3 (33.3%) 1 (20%)  
        400-800 mg 2 (40%)  
*

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

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.

§

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

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