Table 1

Association of clinical and genetic features in CRLF2-rearranged cases in high-risk B-progenitor ALL

CharacteristicDisrupted CRLF2Intact CRLF2Total*P
No. of patients 29 178 207  
Age     
    10 y or older 21 111 132 .405 
    Younger than 10 y 67 75  
Median age, y 14.2 12.8 13.1 > .030 
DS cases     
    DS > .314 
    Not DS 21 134 155  
Sex     
    Male 21 116 137 .529 
    Female 62 70  
WBC, ×1000/μL     
    50 or more 16 92 108 < .842 
    Less than 50 13 86 99  
    Median WBC 92.7 59.6 62.3 < .198 
Ethnicity§     
    Hispanic/Latino 18 33 51 < .001 
    Other 11 143 154  
BCR-ABL1–like GEP     
    Yes 18 20 38 < .001 
    No 11 158 169  
IKZF1 alteration     
    Deletion/mutation 21 35 56 < .001 
    Normal 126 131  
JAK mutations     
    Mutation 18 20 < .001 
    Normal 159 167  
CNS blasts     
    No blasts 19 141 160 < .196 
    Less than 5 20 26  
    5 or more 17 21  
Probability of 4-year RFS 35.3 (9.5) 71.3 (3.6) 66.3 (3.5) .001# 
CharacteristicDisrupted CRLF2Intact CRLF2Total*P
No. of patients 29 178 207  
Age     
    10 y or older 21 111 132 .405 
    Younger than 10 y 67 75  
Median age, y 14.2 12.8 13.1 > .030 
DS cases     
    DS > .314 
    Not DS 21 134 155  
Sex     
    Male 21 116 137 .529 
    Female 62 70  
WBC, ×1000/μL     
    50 or more 16 92 108 < .842 
    Less than 50 13 86 99  
    Median WBC 92.7 59.6 62.3 < .198 
Ethnicity§     
    Hispanic/Latino 18 33 51 < .001 
    Other 11 143 154  
BCR-ABL1–like GEP     
    Yes 18 20 38 < .001 
    No 11 158 169  
IKZF1 alteration     
    Deletion/mutation 21 35 56 < .001 
    Normal 126 131  
JAK mutations     
    Mutation 18 20 < .001 
    Normal 159 167  
CNS blasts     
    No blasts 19 141 160 < .196 
    Less than 5 20 26  
    5 or more 17 21  
Probability of 4-year RFS 35.3 (9.5) 71.3 (3.6) 66.3 (3.5) .001# 

ALL indicates acute lymphoblastic leukemia; DS, Down syndrome; WBC, white blood cell count; GEP, gene expression profiling; CNS, central nervous system; and RFS, relapse-free survival.

*

All 207 patients were used unless otherwise noted.

P values were calculated using Fisher exact test unless otherwise noted.

DS status was available for 163 patients.

§

Ethnicity information was available for 205 patients.

Sequence information was available for 187 patients.

Mann-Whitney test was used to calculate WBC and age continuous variables.

#

Log-rank test used to calculate survival P value.

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