Table 1

Patient characteristics

Patient characteristicsTreatment naive at enrollmentRelapsed at enrollment
Sample size (N = 255 patients), n (%) 198 (78) 57 (22) 
Age, y   
    Median 61 63 
    Range 35-96 46-82 
Sex   
    Female, n (%) 71 (36) 14 (25) 
    Male, n (%) 127 (64) 43 (75) 
Rai stage   
    Low (0), n (%) 91 (46) 10 (17) 
    Intermediate (I-II), n (%) 98 (49) 30 (53) 
    High (III-IV), n (%) 9 (5) 17 (30) 
Median time from diagnosis to enrollment, mo   
    Median 76 
    Range 0-306 5-244 
Median time from enrollment to analysis, mo   
    Median 51 44 
    Range 14-69 14-69 
IgVH mutational status   
    Unmutated (≥ 98% homology to germ line), n (%) 82 (41) 34 (60) 
    Mutated (< 98% homology to germ line), n (%) 108 (55) 20 (35) 
    Not evaluable, n (%) 8 (4) 3 (5) 
Prioritized interphase FISH   
    17p deletion, n (%) 17 (9) 9 (16) 
    11q deletion, n (%) 18 (9) 12 (21) 
    12 trisomy, n (%) 26 (13) 10 (17) 
    Normal karyotype, n (%) 43 (22) 9 (16) 
    13q deletion (sole abnormality), n (%) 90 (45) 16 (28) 
    FISH data not available, n (%) 4 (2) 1 (2) 
Prioritized interphase FISH-25*   
    17p deletion, n (%) 16 (8) 9 (16) 
    11q deletion, n (%) 14 (7) 10 (17) 
    12 trisomy, n (%) 24 (12) 9 (16) 
    Normal karyotype, n (%) 61 (31) 9 (16) 
    13q deletion (sole abnormality), n (%) 79 (40) 19 (33) 
    FISH data not available, n (%) 4 (2) 1 (2) 
ZAP70 expression   
    Negative (≤ 20%), n (%) 116 (59) 19 (33) 
    Positive (> 20%), n (%) 82 (41) 38 (67) 
TP53 exon 2-10 mutations   
    Wild-type, n (%) 174 (88) 45 (79) 
    Mutated, n (%) 24 (12) 12 (21) 
Number of prior therapies   
    Median NA 
    Range NA 1-7 
Patient characteristicsTreatment naive at enrollmentRelapsed at enrollment
Sample size (N = 255 patients), n (%) 198 (78) 57 (22) 
Age, y   
    Median 61 63 
    Range 35-96 46-82 
Sex   
    Female, n (%) 71 (36) 14 (25) 
    Male, n (%) 127 (64) 43 (75) 
Rai stage   
    Low (0), n (%) 91 (46) 10 (17) 
    Intermediate (I-II), n (%) 98 (49) 30 (53) 
    High (III-IV), n (%) 9 (5) 17 (30) 
Median time from diagnosis to enrollment, mo   
    Median 76 
    Range 0-306 5-244 
Median time from enrollment to analysis, mo   
    Median 51 44 
    Range 14-69 14-69 
IgVH mutational status   
    Unmutated (≥ 98% homology to germ line), n (%) 82 (41) 34 (60) 
    Mutated (< 98% homology to germ line), n (%) 108 (55) 20 (35) 
    Not evaluable, n (%) 8 (4) 3 (5) 
Prioritized interphase FISH   
    17p deletion, n (%) 17 (9) 9 (16) 
    11q deletion, n (%) 18 (9) 12 (21) 
    12 trisomy, n (%) 26 (13) 10 (17) 
    Normal karyotype, n (%) 43 (22) 9 (16) 
    13q deletion (sole abnormality), n (%) 90 (45) 16 (28) 
    FISH data not available, n (%) 4 (2) 1 (2) 
Prioritized interphase FISH-25*   
    17p deletion, n (%) 16 (8) 9 (16) 
    11q deletion, n (%) 14 (7) 10 (17) 
    12 trisomy, n (%) 24 (12) 9 (16) 
    Normal karyotype, n (%) 61 (31) 9 (16) 
    13q deletion (sole abnormality), n (%) 79 (40) 19 (33) 
    FISH data not available, n (%) 4 (2) 1 (2) 
ZAP70 expression   
    Negative (≤ 20%), n (%) 116 (59) 19 (33) 
    Positive (> 20%), n (%) 82 (41) 38 (67) 
TP53 exon 2-10 mutations   
    Wild-type, n (%) 174 (88) 45 (79) 
    Mutated, n (%) 24 (12) 12 (21) 
Number of prior therapies   
    Median NA 
    Range NA 1-7 
*

FISH findings in ≥ 25% of nuclei.

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