Table 1.

Comparison of clinical findings between patients with OM-CMML and CMML

CharacteristicOM-CMML (n = 40)CMML (n = 56)d-CMML (n = 40)p-CMML (n = 16)P (OM-CMML vs CMML)P (OM-CMML vs d-CMML)P (OM-CMML vs p-CMML)P (d-CMML vs p-CMML)
Age, median (range), y 77.5 (44-91) 76.5 (60-94) 76.5 (60-88) 77 (61-94) .997 .95 .913 .835 
Male sex, n (%) 27 (68) 29 (52) 21 (52.5) 8 (50) .124 .171 .222 .866 
Hemoglobin, median (range), g/L 11.35 (7.3-14.6) 12.3 (5.4-15.7) 12.55 (8.6-15.7) 11.85 (5.4-14.6) .019 .005 .650 .198 
WBC count, median (range), ×109/L 4.58 (2.49-7.02) 9.03 (2.81-34.82) 7.95 (2.81-12.62) 17.11 (13.18-34.82) < .001 < .001 < .001 < .001 
Neutrophil count, median (range), ×109/L 2.15 (0.38-4.42) 4.86 (0.47-19.62) 3.35 (0.47-7.02) 8.77 (4.67-19.62) < .001 < .001 < .001 < .001 
Platelet count, median (range), ×109/L 138.5 (36-318) 138.5 (15-559) 137 (33-559) 140 (15-294) .565 .462 .986 .618 
Monocyte count, median (range), ×109/L 0.71 (0.53-0.96) 1.96 (1-13.33) 1.67 (1-3.01) 5.02 (2.69-13.33) <.001 <.001 <.001 <.001 
PB monocyte %, median (range) 17 (10-26) 24.85 (13-60) 23.85 (13-42) 28.7 (20-60) <.001 <.001 <.001 .002 
BM monocyte %, median (range) 5 (1-13) 10 (2-27) 9 (2-16) 12 (2-27) <.001 <.001 .001 .175 
BM promonocyte %, median (range) 1 (0-6) 3 (0-14) 2 (0-7) 4 (1-14) <.001 <.001 <.001 .012 
BM blast %, median (range) 3 (0-8) 3 (1-15) 3 (1-9) 4 (1-15) .838 .798 .338 .252 
Dyserythropoiesis, median (range), %  31 (0-80) 23 (0-90) 22 (0-90) 24 (3-77) .04 .026 .411 .252 
 ≥10%, % 74 42.7 71.4 80  .027  .03 .329 .728 
Dysgranulopoiesis, median (range), % 46 (0-100) 44 (0-92) 40 (0-92) 55 (9-78) .917 .636 .530 .233 
 ≥10%, % 87.2 88.5 86.5 93.3 .929 .659 
Dysthrombopoiesis, median (range), %  13 (0-64) 8 (0-69) 7 (0-69) 16 (0-54) .15 .063 .794  .142  
 ≥10%, % 65.7 46.7 42.9 60 .089 .055 .726 .476 
Karyotype, abnormal/total cases (%) 10/38 (26) 9/50 (18) 7/36 (19.4) 2/14 (14.3) .498 .482 .475 .99 
Spanish cytogenetic risk group, n (%)     .384 .559 .546 .809 
 Low 33 (87) 45 (90) 32 (88.9) 13 (92.9) 
 Intermediate 3 (8) 1 (2) 1 (2.8) 0 (0) 
 High 2 (5) 4 (8) 3 (8.3) 1 (7.1) 
Presence PB blasts, n (%) 2/40 (5) 8/50 (16) 3/36 (8.3) 5/15 (33.3) .176 .663 .013 .039 
2017 WHO classification, n (%)     .013 .121 .002 .023 
 CMML-0 22 (55) 13 (25) 12 (32.4) 1 (6.7) .003 .078 .002 .078 
 CMML-1 14 (35) 29 (56) 21 (56.8) 8 (53.3) .048 .055 .354 .822 
 CMML-2 4 (10) 10 (19) 4 (10.8) 6 (40) .256 .99 .018 .024 
Patients with an associated autoimmune disease, n (%)* 4 (10) 5 (9) 4 (10) 1 (6.3) .99 .99 .99 .99 
Number of patients with mutations (%) 40 (100) 52/53 (98) 36/37 (97.3) 16 (100) .99 .481 .99 .99 
Number of mutated genes, median (range) 2 (1-8) 3 (0-5) 2 (0-5) 4 (2-5) .407 .46 .001 <.001 
Number of mutations, median (range) 3 (1-9) 3 (0-9) 3 (0-9) 4.5 (2-7) .134 .859 .002 .003 
CharacteristicOM-CMML (n = 40)CMML (n = 56)d-CMML (n = 40)p-CMML (n = 16)P (OM-CMML vs CMML)P (OM-CMML vs d-CMML)P (OM-CMML vs p-CMML)P (d-CMML vs p-CMML)
Age, median (range), y 77.5 (44-91) 76.5 (60-94) 76.5 (60-88) 77 (61-94) .997 .95 .913 .835 
Male sex, n (%) 27 (68) 29 (52) 21 (52.5) 8 (50) .124 .171 .222 .866 
Hemoglobin, median (range), g/L 11.35 (7.3-14.6) 12.3 (5.4-15.7) 12.55 (8.6-15.7) 11.85 (5.4-14.6) .019 .005 .650 .198 
WBC count, median (range), ×109/L 4.58 (2.49-7.02) 9.03 (2.81-34.82) 7.95 (2.81-12.62) 17.11 (13.18-34.82) < .001 < .001 < .001 < .001 
Neutrophil count, median (range), ×109/L 2.15 (0.38-4.42) 4.86 (0.47-19.62) 3.35 (0.47-7.02) 8.77 (4.67-19.62) < .001 < .001 < .001 < .001 
Platelet count, median (range), ×109/L 138.5 (36-318) 138.5 (15-559) 137 (33-559) 140 (15-294) .565 .462 .986 .618 
Monocyte count, median (range), ×109/L 0.71 (0.53-0.96) 1.96 (1-13.33) 1.67 (1-3.01) 5.02 (2.69-13.33) <.001 <.001 <.001 <.001 
PB monocyte %, median (range) 17 (10-26) 24.85 (13-60) 23.85 (13-42) 28.7 (20-60) <.001 <.001 <.001 .002 
BM monocyte %, median (range) 5 (1-13) 10 (2-27) 9 (2-16) 12 (2-27) <.001 <.001 .001 .175 
BM promonocyte %, median (range) 1 (0-6) 3 (0-14) 2 (0-7) 4 (1-14) <.001 <.001 <.001 .012 
BM blast %, median (range) 3 (0-8) 3 (1-15) 3 (1-9) 4 (1-15) .838 .798 .338 .252 
Dyserythropoiesis, median (range), %  31 (0-80) 23 (0-90) 22 (0-90) 24 (3-77) .04 .026 .411 .252 
 ≥10%, % 74 42.7 71.4 80  .027  .03 .329 .728 
Dysgranulopoiesis, median (range), % 46 (0-100) 44 (0-92) 40 (0-92) 55 (9-78) .917 .636 .530 .233 
 ≥10%, % 87.2 88.5 86.5 93.3 .929 .659 
Dysthrombopoiesis, median (range), %  13 (0-64) 8 (0-69) 7 (0-69) 16 (0-54) .15 .063 .794  .142  
 ≥10%, % 65.7 46.7 42.9 60 .089 .055 .726 .476 
Karyotype, abnormal/total cases (%) 10/38 (26) 9/50 (18) 7/36 (19.4) 2/14 (14.3) .498 .482 .475 .99 
Spanish cytogenetic risk group, n (%)     .384 .559 .546 .809 
 Low 33 (87) 45 (90) 32 (88.9) 13 (92.9) 
 Intermediate 3 (8) 1 (2) 1 (2.8) 0 (0) 
 High 2 (5) 4 (8) 3 (8.3) 1 (7.1) 
Presence PB blasts, n (%) 2/40 (5) 8/50 (16) 3/36 (8.3) 5/15 (33.3) .176 .663 .013 .039 
2017 WHO classification, n (%)     .013 .121 .002 .023 
 CMML-0 22 (55) 13 (25) 12 (32.4) 1 (6.7) .003 .078 .002 .078 
 CMML-1 14 (35) 29 (56) 21 (56.8) 8 (53.3) .048 .055 .354 .822 
 CMML-2 4 (10) 10 (19) 4 (10.8) 6 (40) .256 .99 .018 .024 
Patients with an associated autoimmune disease, n (%)* 4 (10) 5 (9) 4 (10) 1 (6.3) .99 .99 .99 .99 
Number of patients with mutations (%) 40 (100) 52/53 (98) 36/37 (97.3) 16 (100) .99 .481 .99 .99 
Number of mutated genes, median (range) 2 (1-8) 3 (0-5) 2 (0-5) 4 (2-5) .407 .46 .001 <.001 
Number of mutations, median (range) 3 (1-9) 3 (0-9) 3 (0-9) 4.5 (2-7) .134 .859 .002 .003 

Bold P values are statistically significant.

WBC, white blood cell; Spanish cytogenetic risk group: low, normal, and isolated Y chromosome loss; intermediate, other abnormalities except those mentioned in low- and high-risk categories; and high, +8, abnormalities of chromosome 7 and complex karyotype (≥3 abnormalities).

*

Four patients with OM-CMML presented with a concomitant autoimmune disease: 1, antiphospholipid syndrome; 2, systemic scleroses; and 1, immune thrombocytopenic purpura. Five patients with CMML presented with a concomitant autoimmune disease: 1, systemic sclerosis; 1, dermatomyositis; 1, ankylosing spondylitis HLA-B27+; 1, antiphospholipid syndrome; 1, immune thrombocytopenic purpura.

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