Table 1.

Characteristics of 61 patients with aCML or CNL

Whole series (61)aCML (37)CNL (24)P
Gender = % male (n) 65.6% (40) 67.6% (25) 62.5% (15) .765 
Age (mean, range) 69.4 (32.9-92.5) 68.6 (40.6-91.4) 71.2 (33.0-92.5) .692 
Median OS (mo) 17.2 17.7 15.2 .86 
Transformation to AML 29.5% (18) 32.4% (12) 25% (6) .534 
Median time to transformation (mo) 14.3 13.6 15.2 .52 
HSCT 17% (9) 25.8% (8) 4.5% (1) .097 
Cause of death    .737 
Progression 65.6% (21) 63.2% (12) 69.2% (9)  
Bleeding 12.5% (4) 10.5% (2) 15.4% (2)  
Other 21.9% (7) 26.3% (5) 15.4 (2)  
Splenomegaly 55.7% (34) 48.6% (18) 66.7% (16) .263 
Hepatomegaly 21.7% (10) 14.7% (5) 41.7% (5) .124 
Cutaneous bleeding 10.6% (5) 8.6% (3) 16.7% (2) .808 
Mucosal bleeding 4.3% (2) 2.9% (1) 8.3% (1) 1.000 
Hemoglobin (g/L) 83.32 85.73 79.81 .669 
Platelets (×109/L) 303.65 332.83 259.88 .387 
WBCs (×109/L) 62.23 68.15 52.70 .284 
Neutrophils (×109/L) 53.46 57.23 47.89 .486 
Lymphocytes (×109/L) 3.70 4.16 2.96 .069 
Monocytes (×109/L) 1.88 2.43 1.02 .018 
Abnormal cytogenetics 13.5% (7) 19.4% (6) 4.8% (1) .130 
Mutations detected by NGS 100% (53) 100% (30) 100% (23) NA 
Number of mutated genes (mean) 3.47 3.77 3.09 .118 
Mutated CSF3R 59.1% (26) 27.3% (6) 90.9% (20) <.001 
Mutated SETBP1 52.2% (24) 56% (14) 47.6% (10) .787 
Mutated signaling genes 71.7% (38) 63.3% (19) 82.6% (19) .216 
Mutated transcription factor genes 22.6% (12) 30% (9) 13.0% (3) .258 
Mutated tumor suppressor genes 1.9% (1) 3.3% (1) 0% (0) 1.000 
Mutated epigenetic modifier genes 88.7% (47) 93.3% (28) 82.6% (19) .433 
Mutated splicing factor genes 56.6% (30) 53.3% (16) 60.9% (14) .788 
Mutated Cohesins and other genes 17% (9) 16.7% (5) 17.4% (4) 1.000 
Whole series (61)aCML (37)CNL (24)P
Gender = % male (n) 65.6% (40) 67.6% (25) 62.5% (15) .765 
Age (mean, range) 69.4 (32.9-92.5) 68.6 (40.6-91.4) 71.2 (33.0-92.5) .692 
Median OS (mo) 17.2 17.7 15.2 .86 
Transformation to AML 29.5% (18) 32.4% (12) 25% (6) .534 
Median time to transformation (mo) 14.3 13.6 15.2 .52 
HSCT 17% (9) 25.8% (8) 4.5% (1) .097 
Cause of death    .737 
Progression 65.6% (21) 63.2% (12) 69.2% (9)  
Bleeding 12.5% (4) 10.5% (2) 15.4% (2)  
Other 21.9% (7) 26.3% (5) 15.4 (2)  
Splenomegaly 55.7% (34) 48.6% (18) 66.7% (16) .263 
Hepatomegaly 21.7% (10) 14.7% (5) 41.7% (5) .124 
Cutaneous bleeding 10.6% (5) 8.6% (3) 16.7% (2) .808 
Mucosal bleeding 4.3% (2) 2.9% (1) 8.3% (1) 1.000 
Hemoglobin (g/L) 83.32 85.73 79.81 .669 
Platelets (×109/L) 303.65 332.83 259.88 .387 
WBCs (×109/L) 62.23 68.15 52.70 .284 
Neutrophils (×109/L) 53.46 57.23 47.89 .486 
Lymphocytes (×109/L) 3.70 4.16 2.96 .069 
Monocytes (×109/L) 1.88 2.43 1.02 .018 
Abnormal cytogenetics 13.5% (7) 19.4% (6) 4.8% (1) .130 
Mutations detected by NGS 100% (53) 100% (30) 100% (23) NA 
Number of mutated genes (mean) 3.47 3.77 3.09 .118 
Mutated CSF3R 59.1% (26) 27.3% (6) 90.9% (20) <.001 
Mutated SETBP1 52.2% (24) 56% (14) 47.6% (10) .787 
Mutated signaling genes 71.7% (38) 63.3% (19) 82.6% (19) .216 
Mutated transcription factor genes 22.6% (12) 30% (9) 13.0% (3) .258 
Mutated tumor suppressor genes 1.9% (1) 3.3% (1) 0% (0) 1.000 
Mutated epigenetic modifier genes 88.7% (47) 93.3% (28) 82.6% (19) .433 
Mutated splicing factor genes 56.6% (30) 53.3% (16) 60.9% (14) .788 
Mutated Cohesins and other genes 17% (9) 16.7% (5) 17.4% (4) 1.000 

P for differences between aCML and CNL. Statistically significant differences are in bold.

HSCT, hematopoietic stem cell transplant.

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