Table 2.

Univariable analysis of effect of molecular-genetic features on survival

FactorHR95% CIP
Cytogenetic risk*    
 Low Reference   
 Intermediate 0.71 0.42-1.18 .18 
 High 1.19 0.71-1.97 .51 
Mutation    
 TET2 1.11 0.76-1.61 .60 
 ASXL1 1.45 1.00-2.10 .05 
 NRAS 1.67 1.11-2.52 .01 
 KRAS 1.34 0.78-2.32 .29 
 SETBP1 0.91 0.55-1.53 .73 
 JAK2 0.80 0.37-1.71 .56 
 CBL 1.08 0.62-1.68 .95 
 DNMT3A 0.90 0.57-1.44 .68 
 EZH2 1.09 0.62-1.91 .76 
 IDH1 1.28 0.68-2.38 .44 
 IDH2 0.67 0.25-1.83 .44 
 ZRSR2 0.74 0.40-1.38 .34 
 U2AF1 0.93 0.55-1.58 .79 
 SH2B3 1.09 0.48-2.48 .83 
 SRSF2 1.28 0.88-1.86 .19 
 ETV6 0.75 0.18-3.02 .68 
 TP53 1.31 0.70-2.42 .40 
 RUNX1 1.27 0.83-1.95 .26 
 SF3B1 0.86 0.44-1.71 .68 
No. of mutations    
 Continuous 1.09 0.98-1.22 .10 
 0-2 Reference   
 >2 1.39 0.97-2.01 .08 
Genetic risk    
 Low Reference   
 Intermediate-1 0.96 0.57-1.62 .88 
 Intermediate-2 1.02 0.56-1.85 .95 
 High 1.34 0.79-2.27 .27 
FactorHR95% CIP
Cytogenetic risk*    
 Low Reference   
 Intermediate 0.71 0.42-1.18 .18 
 High 1.19 0.71-1.97 .51 
Mutation    
 TET2 1.11 0.76-1.61 .60 
 ASXL1 1.45 1.00-2.10 .05 
 NRAS 1.67 1.11-2.52 .01 
 KRAS 1.34 0.78-2.32 .29 
 SETBP1 0.91 0.55-1.53 .73 
 JAK2 0.80 0.37-1.71 .56 
 CBL 1.08 0.62-1.68 .95 
 DNMT3A 0.90 0.57-1.44 .68 
 EZH2 1.09 0.62-1.91 .76 
 IDH1 1.28 0.68-2.38 .44 
 IDH2 0.67 0.25-1.83 .44 
 ZRSR2 0.74 0.40-1.38 .34 
 U2AF1 0.93 0.55-1.58 .79 
 SH2B3 1.09 0.48-2.48 .83 
 SRSF2 1.28 0.88-1.86 .19 
 ETV6 0.75 0.18-3.02 .68 
 TP53 1.31 0.70-2.42 .40 
 RUNX1 1.27 0.83-1.95 .26 
 SF3B1 0.86 0.44-1.71 .68 
No. of mutations    
 Continuous 1.09 0.98-1.22 .10 
 0-2 Reference   
 >2 1.39 0.97-2.01 .08 
Genetic risk    
 Low Reference   
 Intermediate-1 0.96 0.57-1.62 .88 
 Intermediate-2 1.02 0.56-1.85 .95 
 High 1.34 0.79-2.27 .27 
*

As defined in Such et al12 : low, normal and isolated -Y; intermediate, other abnormalities; and high, trisomy 8, complex karyotype (≥3 abnormalities), and abnormalities of chromosome 7.

As defined in Elenea et al15 : cytogenetic risk, presence or absence of ASXL1 and/or NRAS and/or RUNX1 and/or SETBP1 mutations.

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