Table 2

Multivariate analysis on overall survival

Prognostic factorParameter estimateSEHazard ratio95% CI of hazard ratioP
Treatment group: tipifarnib vs BSC 0.049 0.114 1.050 (0.84-1.314) .667 
Age: ≥ 75 vs < 75 0.252 0.116 1.287 (1.025-1.616) .030 
ECOG: 2 vs 0 and 1 0.832 0.131 2.298 (1.778-2.97) .000 
Unfavorable cytogenetics: yes vs no 0.564 0.120 1.758 (1.39-2.223) .000 
AML with myelodysplasia vs AML without myelodysplasia −0.089 0.124 0.915 (0.718-1.166) .473 
LDH U/L: > 1500 vs ≤ 1500 0.081 0.271 1.085 (0.638-1.845) .764 
WBC count: > 25 giga/L vs ≤ 25 giga/L 0.214 0.172 1.239 (0.884-1.736) .213 
Bone marrow blasts: > 50% vs ≤ 50% 0.542 0.124 1.719 (1.347-2.194) .000 
Prognostic factorParameter estimateSEHazard ratio95% CI of hazard ratioP
Treatment group: tipifarnib vs BSC 0.049 0.114 1.050 (0.84-1.314) .667 
Age: ≥ 75 vs < 75 0.252 0.116 1.287 (1.025-1.616) .030 
ECOG: 2 vs 0 and 1 0.832 0.131 2.298 (1.778-2.97) .000 
Unfavorable cytogenetics: yes vs no 0.564 0.120 1.758 (1.39-2.223) .000 
AML with myelodysplasia vs AML without myelodysplasia −0.089 0.124 0.915 (0.718-1.166) .473 
LDH U/L: > 1500 vs ≤ 1500 0.081 0.271 1.085 (0.638-1.845) .764 
WBC count: > 25 giga/L vs ≤ 25 giga/L 0.214 0.172 1.239 (0.884-1.736) .213 
Bone marrow blasts: > 50% vs ≤ 50% 0.542 0.124 1.719 (1.347-2.194) .000 

Regression analysis of survival data (number of observations used = 362) was based on Cox proportional hazards model.

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