Table 1

Higher dexamethasone clearance was associated with cumulative incidence of any (hematologic, CNS, and other) relapse

Factors*Hazard ratio95% CIP
Dexamethasone CL/F (L/h per m2) per 50-unit change 1.56 1.1-2.19 .0104 
Anti–ASP antibody positive vs negative 0.57 0.09-3.76 .56 
ASP antibody timing§ 0.74 0.23-2.36 .61 
Older than 10 years vs 1-10 years 0.61 0.23-1.59 .31 
Initial leukocyte count ≥ 100 cells/mm3 vs < 100 cells/mm3 1.87 0.57-6.16 .30 
Black vs white 2.84 1.13-7.1 .0261 
Other vs white 1.22 0.33-4.42 .76 
T-lineage vs B-lineage 1.63 0.67-4.0 .28 
MRD 46 positive vs negative# 1.31 0.48-3.62 .60 
SR/HR vs LR 5.99 1.80-19.97 .0035 
Factors*Hazard ratio95% CIP
Dexamethasone CL/F (L/h per m2) per 50-unit change 1.56 1.1-2.19 .0104 
Anti–ASP antibody positive vs negative 0.57 0.09-3.76 .56 
ASP antibody timing§ 0.74 0.23-2.36 .61 
Older than 10 years vs 1-10 years 0.61 0.23-1.59 .31 
Initial leukocyte count ≥ 100 cells/mm3 vs < 100 cells/mm3 1.87 0.57-6.16 .30 
Black vs white 2.84 1.13-7.1 .0261 
Other vs white 1.22 0.33-4.42 .76 
T-lineage vs B-lineage 1.63 0.67-4.0 .28 
MRD 46 positive vs negative# 1.31 0.48-3.62 .60 
SR/HR vs LR 5.99 1.80-19.97 .0035 

ASP indicates asparaginase; and MRD 46, minimal residual disease at the end of remission induction.

*

Prognostic features included in this model are known to be associated with treatment outcome in St Jude Total XV cohort by univariate analysis.

P value from multivariate analysis using Fine and Gray regression model.18 

Dexamethasone clearance is continuous variable, and the hazard ratio is calculated for every 50-unit change in clearance.

§

Timing when the patients first tested positive for anti–asparaginase antibody.

Genetically determined race as described.10 

Acute lymphoblastic leukemia immunophenotype.

#

MRD positive is ≥ 0.01% (1 or more lymphoblasts among 104 mononuclear cells in the bone marrow) and MRD negative is < 0.01% lymphoblasts in the bone marrow sample.

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