Table 1

Main clinical and hematologic characteristics at diagnosis in the training and validation cohorts

CharacteristicTraining seriesValidation series
Median (range)N (%)Median (range)N (%)P value*
Overall  558 (100)  274 (100)  
Age, y 73 (19-99)  70 (41-98)  <.001 
 ≤60  61 (11)  55 (20) <.001 
 61-70  135 (24)  105 (38) 
 >70  362 (65)  114 (42) 
Gender      
 Male  377 (68)  191 (70) .532§ 
 Female  181 (32)  83 (30) 
WHO subtype      
 CMML-1  478 (86)  218 (80) .025 
 CMML-2  80 (14)  56 (20) 
Hemoglobin level, g/dL 11 (1-19)  11 (2-17)  .224 
 <10 g/dL  190 (34)  101 (37) .479§ 
 ≥10 g/dL  368 (66)  173 (63) 
Leukocyte count, × 109/L 10 (1-156)  13 (1-150)  .143 
 <13 × 109/L (CMML-MD FAB subtype)  338 (61)  138 (50) .005§ 
 ≥13 × 109/L (CMML-MP FAB subtype)  220 (39)  136 (50) 
Platelet count, × 109/L 123 (4-928)  105 (1-979)  .091 
 <100 × 109/L  221 (40)  132 (48) .019§ 
 ≥100 × 109/L  337 (60)  142 (52) 
Neutrophil count, × 109/L 4.2 (0.1-73.9)  6.3 (0.1-75.0)  .018 
 <1.8 × 109/L  103 (18)  41 (15) .218§ 
 ≥1.8 × 109/L  455 (82)  232 (85) 
Monocyte count, × 109/L 2.6 (1.1-40.9)  6.4 (1.1-75.0)  <.001 
 <3.0 × 109/L  236 (57)  128 (47) .010§ 
 ≥3.0 × 109/L  180 (43)  146 (53) 
Blasts in PB      
 Absent  367 (79)  193 (70) .013§ 
 Present  100 (21)  81 (30) 
Blasts in BM, % 3 (0-19)  6 (0-19)  <.001 
 <5  347 (62)  116 (42) <.001 
 5-9  138 (25)  103 (38) 
 10-19  73 (13)  55 (20) 
LDH level, U/L 394 (104-2976)  277 (97-7743)  <.001 
 ≤480 UI/L  242 (68)  94 (46) <.001§ 
 >480 UI/L  115 (32)  109 (54) 
Ferritin level, mg/dL 170 (6-4000)  318 (58-2010)  .001 
 ≤500 mg/dL  173 (80)  73 (63) <.001§ 
 >500 mg/dL  43 (20)  43 (37) 
RBC transfusion dependency||      
 No  441 (79)  205 (75) .156§ 
 Yes  116 (21)  69 (25) 
CMML-specific cytogenetic risk classification      
 Low  429 (81)  146 (63) <.001 
 Intermediate  47 (9)  41 (18) 
 High  56 (10)  45 (19) 
CharacteristicTraining seriesValidation series
Median (range)N (%)Median (range)N (%)P value*
Overall  558 (100)  274 (100)  
Age, y 73 (19-99)  70 (41-98)  <.001 
 ≤60  61 (11)  55 (20) <.001 
 61-70  135 (24)  105 (38) 
 >70  362 (65)  114 (42) 
Gender      
 Male  377 (68)  191 (70) .532§ 
 Female  181 (32)  83 (30) 
WHO subtype      
 CMML-1  478 (86)  218 (80) .025 
 CMML-2  80 (14)  56 (20) 
Hemoglobin level, g/dL 11 (1-19)  11 (2-17)  .224 
 <10 g/dL  190 (34)  101 (37) .479§ 
 ≥10 g/dL  368 (66)  173 (63) 
Leukocyte count, × 109/L 10 (1-156)  13 (1-150)  .143 
 <13 × 109/L (CMML-MD FAB subtype)  338 (61)  138 (50) .005§ 
 ≥13 × 109/L (CMML-MP FAB subtype)  220 (39)  136 (50) 
Platelet count, × 109/L 123 (4-928)  105 (1-979)  .091 
 <100 × 109/L  221 (40)  132 (48) .019§ 
 ≥100 × 109/L  337 (60)  142 (52) 
Neutrophil count, × 109/L 4.2 (0.1-73.9)  6.3 (0.1-75.0)  .018 
 <1.8 × 109/L  103 (18)  41 (15) .218§ 
 ≥1.8 × 109/L  455 (82)  232 (85) 
Monocyte count, × 109/L 2.6 (1.1-40.9)  6.4 (1.1-75.0)  <.001 
 <3.0 × 109/L  236 (57)  128 (47) .010§ 
 ≥3.0 × 109/L  180 (43)  146 (53) 
Blasts in PB      
 Absent  367 (79)  193 (70) .013§ 
 Present  100 (21)  81 (30) 
Blasts in BM, % 3 (0-19)  6 (0-19)  <.001 
 <5  347 (62)  116 (42) <.001 
 5-9  138 (25)  103 (38) 
 10-19  73 (13)  55 (20) 
LDH level, U/L 394 (104-2976)  277 (97-7743)  <.001 
 ≤480 UI/L  242 (68)  94 (46) <.001§ 
 >480 UI/L  115 (32)  109 (54) 
Ferritin level, mg/dL 170 (6-4000)  318 (58-2010)  .001 
 ≤500 mg/dL  173 (80)  73 (63) <.001§ 
 >500 mg/dL  43 (20)  43 (37) 
RBC transfusion dependency||      
 No  441 (79)  205 (75) .156§ 
 Yes  116 (21)  69 (25) 
CMML-specific cytogenetic risk classification      
 Low  429 (81)  146 (63) <.001 
 Intermediate  47 (9)  41 (18) 
 High  56 (10)  45 (19) 
*

P value is the statistical comparison of the different characteristics in training and validation series.

Mann-Whitney U test.

χ2 test.

§

Fisher’s exact test.

||

RBC transfusion dependency was defined as having at least 1 RBC transfusion every 8 weeks over a period of 4 months.

CMML-specific cytogenetic risk classification: low, normal and isolated –Y; intermediate, other abnormalities; and high, trisomy 8, complex karyotype (≥3 abnormalities), and abnormalities of chromosome 7.

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