Table 4.

Multivariate analyses models for response and survival after induction chemotherapy in AML patients experiencing HMA failure

VariableORR, %OR95% CIP
Cytogenetic risk   0.16-1.54 .20 
 Favorable/intermediate 37.5 
 Unfavorable 21.1 0.42 
Anthracyclines   0.57-10.37 .23 
 No 18.8 
 Yes 37.2 2.43 
VariableORR, %OR95% CIP
Cytogenetic risk   0.16-1.54 .20 
 Favorable/intermediate 37.5 
 Unfavorable 21.1 0.42 
Anthracyclines   0.57-10.37 .23 
 No 18.8 
 Yes 37.2 2.43 
VariableMedian OS, moHR95% CIP
Therapy related   0.66- 2.90 .39 
 No 7.8 
 Yes 4.4 1.4 
Cytogenetic risk   0.79-2.9 .21 
 Favorable/intermediate 7.9 
 Unfavorable 4.5 1.5 
Prior induction   0.74-3.14 .25 
 No 7.8 
 Yes 3.7 1.5 
Disease status at HMA failure   1.19-5.98 .02 
 Stable 7.9 
 Progressive 4.0 2.66 
Use of anthracyclines   0.17-0.82 .01 
 No 3.7 
 Yes 0.37 
VariableMedian OS, moHR95% CIP
Therapy related   0.66- 2.90 .39 
 No 7.8 
 Yes 4.4 1.4 
Cytogenetic risk   0.79-2.9 .21 
 Favorable/intermediate 7.9 
 Unfavorable 4.5 1.5 
Prior induction   0.74-3.14 .25 
 No 7.8 
 Yes 3.7 1.5 
Disease status at HMA failure   1.19-5.98 .02 
 Stable 7.9 
 Progressive 4.0 2.66 
Use of anthracyclines   0.17-0.82 .01 
 No 3.7 
 Yes 0.37 

Logistic regression multivariate analysis model and Cox model for multivariate analysis of OS after induction therapy, including all covariates with a potential outcome on response in univariate analysis (P value in univariate <.15). Cytogenetic risk was evaluated per AML UK MRC classification.

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