Table 4

Multivariable analyses in the training cohort

VariableOS
PFS
Relapse
NRM
HRPHRPHRPHRP
Risk group (DRI)         
    Low 0.6 < .0001 0.6 < .0001 0.4 < .0001 1.0 0.9 
    Intermediate Ref  Ref  Ref  Ref  
    High 1.8 < .0001 1.9 < .0001 2.0 < .0001 1.1 .6 
    Very high 3.1 < .0001 3.2 < .0001 2.5 .0002 1.2 .5 
Age, y         
    < 40 0.7 < .0001 0.7 .0005 1.1 .7 0.6 < .0001 
    40-54 Ref  Ref  Ref  Ref  
    55-64 1.1 .4 1.0 .6 0.9 .6 1.2 .2 
    ≥ 65 1.2 .10 1.0 .7 1.1 .3 0.7 .12 
HSCT on protocol         
    No Ref  Ref  Ref  Ref  
    Yes 0.7 < .0001 0.7 < .0001 0.8 .009 1.1 .6 
Donor         
    MRD 0.8 .03 1.0 .8 1.5 < .0001 0.5 < .0001 
    MUD Ref .0007 Ref .004 Ref .9 Ref .004 
    Mismatched 1.5  1.4  1.0  1.6  
Graft source         
    BM Ref  Ref  Ref  Ref  
    PB N/Aa  N/Aa  0.8 .09 1.0 .8 
    UCB 1.5 .13 1.4 .17 0.7 .11 1.9 .017 
Conditioning N/Aa  N/Aa      
    MAC     Ref  Ref  
    RIC     3.0 < .0001 0.3 < .0001 
GVHD prophylaxis         
    CnI/Mtx Ref  Ref  Ref  Ref  
    CnI/Siro ± Mtx 1.0 .9 1.1 .5 1.2 .08 0.7 .007 
    CnI/MMF 0.9 .6 0.8 .3 0.9 .6 1.0 1.0 
    TCD 1.6 .04 1.5 .08 1.3 .5 1.4 .3 
    Other 2.0 .005 1.6 .04 1.0 .9 1.8 .08 
CMV serostatus         
    Donor and patient − Ref  Ref  Ref  Ref  
    Donor or patient + 1.1 .4 1.0 1.0 0.9 .5 1.1 .4 
Patient sex         
    Male Ref  Ref  Ref  Ref  
    Female 0.9 .03 0.9 .2 1.1 .3 0.8 .018 
Therapy-related disease         
    No Ref  Ref  Ref  Ref  
    Yes 1.0 .9 0.9 .3 0.8 .16 1.0 .9 
Transformed disease         
    No Ref  Ref  Ref  Ref  
    Yes 1.1 .3 1.2 .13 1.2 .3 1.1 .7 
Year of HSCT* N/A*  N/A*  N/A*  N/A*  
VariableOS
PFS
Relapse
NRM
HRPHRPHRPHRP
Risk group (DRI)         
    Low 0.6 < .0001 0.6 < .0001 0.4 < .0001 1.0 0.9 
    Intermediate Ref  Ref  Ref  Ref  
    High 1.8 < .0001 1.9 < .0001 2.0 < .0001 1.1 .6 
    Very high 3.1 < .0001 3.2 < .0001 2.5 .0002 1.2 .5 
Age, y         
    < 40 0.7 < .0001 0.7 .0005 1.1 .7 0.6 < .0001 
    40-54 Ref  Ref  Ref  Ref  
    55-64 1.1 .4 1.0 .6 0.9 .6 1.2 .2 
    ≥ 65 1.2 .10 1.0 .7 1.1 .3 0.7 .12 
HSCT on protocol         
    No Ref  Ref  Ref  Ref  
    Yes 0.7 < .0001 0.7 < .0001 0.8 .009 1.1 .6 
Donor         
    MRD 0.8 .03 1.0 .8 1.5 < .0001 0.5 < .0001 
    MUD Ref .0007 Ref .004 Ref .9 Ref .004 
    Mismatched 1.5  1.4  1.0  1.6  
Graft source         
    BM Ref  Ref  Ref  Ref  
    PB N/Aa  N/Aa  0.8 .09 1.0 .8 
    UCB 1.5 .13 1.4 .17 0.7 .11 1.9 .017 
Conditioning N/Aa  N/Aa      
    MAC     Ref  Ref  
    RIC     3.0 < .0001 0.3 < .0001 
GVHD prophylaxis         
    CnI/Mtx Ref  Ref  Ref  Ref  
    CnI/Siro ± Mtx 1.0 .9 1.1 .5 1.2 .08 0.7 .007 
    CnI/MMF 0.9 .6 0.8 .3 0.9 .6 1.0 1.0 
    TCD 1.6 .04 1.5 .08 1.3 .5 1.4 .3 
    Other 2.0 .005 1.6 .04 1.0 .9 1.8 .08 
CMV serostatus         
    Donor and patient − Ref  Ref  Ref  Ref  
    Donor or patient + 1.1 .4 1.0 1.0 0.9 .5 1.1 .4 
Patient sex         
    Male Ref  Ref  Ref  Ref  
    Female 0.9 .03 0.9 .2 1.1 .3 0.8 .018 
Therapy-related disease         
    No Ref  Ref  Ref  Ref  
    Yes 1.0 .9 0.9 .3 0.8 .16 1.0 .9 
Transformed disease         
    No Ref  Ref  Ref  Ref  
    Yes 1.1 .3 1.2 .13 1.2 .3 1.1 .7 
Year of HSCT* N/A*  N/A*  N/A*  N/A*  

CnI indicates calcineurin inhibitor; DRI, disease risk index (see text); HR, hazard ratio; MAC, myeloablative conditioning; MMF, mycophenolate mofetil; MRD, matched related donor; MTX, methotrexate; MUD, matched unrelated donor; N/A, not applicable; OS, overall survival; PB, peripheral blood; PFS, progression-free survival; RIC, reduced-intensity conditioning; Siro, sirolimus; TCD, T-cell depletion; and UCB, umbilical cord blood.

*

OS and PFS models are stratified on conditioning intensity, graft source (BM vs PB), and year of transplantation (2000-2001, 2002-2004, 2005-2009), so no HRs or P values are provided for those variables.

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