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. 2020 Jan 5;9(4):1572–1580. doi: 10.1002/cam4.2740

Table 2.

Risk factors for early mortality in elderly patients with newly diagnosed acute myeloid leukemia

Predictive variables n No. of events Univariate analysis Multivariate analysisa
HR (95% CI) P value HR (95% CI) P value
Age ≥ 80 96 36 1.80 (1.16‐2.80) .009 1.88 (1.08‐3.30) .027
Sex (male) 171 52 1.20 (0.76‐1.91) .436    
Secondary AML 94 31 1.27 (0.81‐1.99) .307    
Therapy‐related AML 25 10 1.59 (0.82‐3.09) .169    
Antecedent hematologic disorder 42 17 1.67 (0.98‐2.85) .062 1.78 (0.96‐3.30) .066
AML‐MRC 82 24 0.97 (0.60‐1.56) .897    
APL 11 2 0.58 (0.14‐2.36) .446    
Comorbidities
Diabetes mellitus 93 23 0.80 (0.49‐1.30) .370    
Hypertension 127 38 1.10 (0.71‐1.72) .660    
Myocardial infarction 54 21 1.60 (0.97‐2.64) .065 1.87 (1.08‐3.24) .025
Ulcer disease 45 17 1.58 (0.92‐2.71) .094 1.21 (0.65‐2.24) .553
ECOG ≥ 2 116/270 46 2.73 (1.71‐4.38) <.001 2.10 (1.22‐3.63) .008
Cytogenetics and molecular abnormalities
NPM1 20/125 2 0.39 (0.09‐1.64) .199    
FLT3‐ITD 18/125 4 1.11 (0.39‐3.22) .841    
Complex karyotype 58/263 22 1.90 (1.15‐3.14) .013 3.21 (1.80‐5.71) <.001
Cytogenetics and molecular risk
Favorable 36/263 7 Reference      
Intermediate 133/263 36 1.44 (0.64‐3.25) .374    
Poor/adverseb 94/263 28 1.72 (0.75‐3.93) .201    
Lab data
Bone marrow blasts ≥ 70% 157/263 50 1.65 (1.00‐2.73) .049 1.88 (1.07‐3.32) .029
Presence of blasts in peripheral blood 182/275 59 1.47 (0.89‐2.44) .135    
White blood cell count ≥ 100 K/µL 26 15 3.19 (1.82‐5.62) <.001 3.31 (1.59‐6.90) .001
Absolute neutrophil count < 500/µL 82 19 0.72 (0.43‐1.20) .209    
Hemoglobin < 10 g/dL 231 63 0.76 (0.44‐1.31) .320    
Platelets < 20 000/µL 45 16 1.45 (0.84‐2.51) .184    
eGFR < 45 63/274 30 2.71 (1.72‐4.28) <.001 2.60 (1.54‐4.39) <.001

Abbreviations: AML, acute myeloid leukemia; AML‐MRC, acute myeloid leukemia with myelodysplasia‐related changes; APL, acute promyelocytic leukemia; CI, confidence interval; ECOG, Eastern Cooperative Oncology Group performance; eGFR, estimated Glomerular filtration rate; HR, hazard ratio.

a

All factors with P < .1 in the univariate analysis were included in the Cox multivariate analysis.

b

Poor/adverse risk was defined as complex (≥3 clonal chromosomal abnormalities), monosomal karyotype, −5, 5q‐, −7, 7q‐, 11q23 ‐ non t(9;11), inv(3), t(3;3), t(6;9), t(9;22), or FLT3‐ITD mutation with wild‐type NPM1.