Table 1.

Demographic and clinical characteristics of the study population in total, and assigned according to degree of CR (sCR or non-sCR)

CharacteristicAll (N = 769)sCR (n = 360)Non-sCR (n = 409)
N%N%N%
Age, y       
 Median (IQR) 56.6 (45.4-65.3) 39.3 54.5 (43.4-64.0) 35.3 58.6 (47.2-65.7) 42.8 
 ≥60 302  127  175  
Sex       
 Male 406 52.8 180 50.0 226 55.3 
 Female 363 47.2 180 50.0 183 44.7 
Year of diagnosis       
 2000-2002 199 25.9 66 18.3 133 32.5 
 2003-2010 570 74.1 294 81.7 276 67.5 
WHO performance score at diagnosis       
 <2 647 84.1 306 85.0 341 83.4 
 ≥2 122 15.9 54 15.0 68 16.6 
AML classification       
 De novo 638 83.0 311 86.4 327 80.0 
 Secondary* 105 13.7 38 10.6 67 16.4 
 Therapy related 26 3.4 11 3.1 15 3.7 
Cytogenetic risk group       
 Favorable 49 5.2 20 5.6 20 4.9 
 Intermediate 554 72.0 258 71.7 296 72.4 
 Unfavorable 104 13.5 58 16.1 46 11.2 
 Missing 71 9.2 24 6.7 47 11.5 
Characteristics at time of diagnosis, median (IQR)       
 Bone marrow blast count, % 55 (33-80)  60 (35-80)  51 (32-80)  
 Blast count blood, % 29 (9-65)  28 (8-70)  30 (4-59)  
 Leukocytes, × 109/L 10.8 (2.4-44.7)  11.1 (2.8-42.8)  9.7 (2.2-46)  
 Platelets, × 109/L 54 (30-103)  63 (33-122.5)  49 (25-86)  
Days between the first day of treatment and CR evaluation (IQR) 31 (27-35)  30 (27-35)  31 (27-37)  
Days at risk for RBC transfusion (IQR) 8 (6-13)  7 (6-13)  8 (6-12)  
CharacteristicAll (N = 769)sCR (n = 360)Non-sCR (n = 409)
N%N%N%
Age, y       
 Median (IQR) 56.6 (45.4-65.3) 39.3 54.5 (43.4-64.0) 35.3 58.6 (47.2-65.7) 42.8 
 ≥60 302  127  175  
Sex       
 Male 406 52.8 180 50.0 226 55.3 
 Female 363 47.2 180 50.0 183 44.7 
Year of diagnosis       
 2000-2002 199 25.9 66 18.3 133 32.5 
 2003-2010 570 74.1 294 81.7 276 67.5 
WHO performance score at diagnosis       
 <2 647 84.1 306 85.0 341 83.4 
 ≥2 122 15.9 54 15.0 68 16.6 
AML classification       
 De novo 638 83.0 311 86.4 327 80.0 
 Secondary* 105 13.7 38 10.6 67 16.4 
 Therapy related 26 3.4 11 3.1 15 3.7 
Cytogenetic risk group       
 Favorable 49 5.2 20 5.6 20 4.9 
 Intermediate 554 72.0 258 71.7 296 72.4 
 Unfavorable 104 13.5 58 16.1 46 11.2 
 Missing 71 9.2 24 6.7 47 11.5 
Characteristics at time of diagnosis, median (IQR)       
 Bone marrow blast count, % 55 (33-80)  60 (35-80)  51 (32-80)  
 Blast count blood, % 29 (9-65)  28 (8-70)  30 (4-59)  
 Leukocytes, × 109/L 10.8 (2.4-44.7)  11.1 (2.8-42.8)  9.7 (2.2-46)  
 Platelets, × 109/L 54 (30-103)  63 (33-122.5)  49 (25-86)  
Days between the first day of treatment and CR evaluation (IQR) 31 (27-35)  30 (27-35)  31 (27-37)  
Days at risk for RBC transfusion (IQR) 8 (6-13)  7 (6-13)  8 (6-12)  

IQR, interquartile range; RBC, red blood cell; WHO, World Health Organization.

*

Defined as AML in patients with prior hematological disease predisposing for AML.

Days between bone marrow evaluation and the first day of following treatment.

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