Table 1.

Demographics, clinical characteristics, and treatment components of patients with extreme hyperleukocytosis at presentation

CharacteristicNumber of patients (%)Median (range)
Total cohort 37 (100)  
Age (y) 37 (100) 43 (1-73) 
Sex   
Male 16 (43)  
Female 21 (57)  
WBC count (×109/L) 37 (100) 124.0 (96.7-297.0) 
Platelet count (×109/L) 34 (92) 33 (5-92) 
Hemoglobin (g/L) 34 (92) 100 (36-142) 
Fibrinogen (g/L) 34 (92) 1.3 (0.2-5.4) 
D-dimers (mg/L)  22 (59) 8.0 (>0.08-74.8) 
Hemorrhagic manifestations   
Yes  26 (70)  
No 9 (24)  
Unknown 2 (5)  
Thrombotic manifestations   
Yes  8 (22)  
No 26 (70)  
Unknown 3 (8)  
Karyotype   
t(15;17) only 25 (68)  
t(15;17) + additional abnormalities 3 (8)  
FISH only 1 (3)  
Normal 1 (3)  
Unknown 7 (19)  
PML breakpoint   
bcr1/2 10 (27)  
bcr3 19 (51)  
Unknown 8 (22)  
FLT3 ITD   
Yes 11 (30)  
No 4 (11)  
Unknown 22 (59)  
FLT3 TKD   
Yes 1 (3)  
No 12 (32)  
Unknown 24 (65)  
Presentation   
Early (>10 years before analysis) 15 (41)  
Late (<10 years before analysis) 22 (59)  
Induction   
ATRA + anthracycline + cytarabine and/or hydroxyurea 13 (35)  
ATRA + anthracycline 12 (32)  
ATRA + anthracycline + ATO + cytarabine and/or hydroxyurea 7 (19)  
ATRA + anthracycline + ATO 4 (11)  
ATRA + hydroxyurea 1 (3)  
Consolidation   
ATRA + chemotherapy 14 (50)  
ATRA + ATO 13 (46)  
ATRA + ATO + chemotherapy 1 (4)  
Maintenance   
ATRA + 6MP + MTX 12 (100)  
ATRA + ATO 0 (0)  
CharacteristicNumber of patients (%)Median (range)
Total cohort 37 (100)  
Age (y) 37 (100) 43 (1-73) 
Sex   
Male 16 (43)  
Female 21 (57)  
WBC count (×109/L) 37 (100) 124.0 (96.7-297.0) 
Platelet count (×109/L) 34 (92) 33 (5-92) 
Hemoglobin (g/L) 34 (92) 100 (36-142) 
Fibrinogen (g/L) 34 (92) 1.3 (0.2-5.4) 
D-dimers (mg/L)  22 (59) 8.0 (>0.08-74.8) 
Hemorrhagic manifestations   
Yes  26 (70)  
No 9 (24)  
Unknown 2 (5)  
Thrombotic manifestations   
Yes  8 (22)  
No 26 (70)  
Unknown 3 (8)  
Karyotype   
t(15;17) only 25 (68)  
t(15;17) + additional abnormalities 3 (8)  
FISH only 1 (3)  
Normal 1 (3)  
Unknown 7 (19)  
PML breakpoint   
bcr1/2 10 (27)  
bcr3 19 (51)  
Unknown 8 (22)  
FLT3 ITD   
Yes 11 (30)  
No 4 (11)  
Unknown 22 (59)  
FLT3 TKD   
Yes 1 (3)  
No 12 (32)  
Unknown 24 (65)  
Presentation   
Early (>10 years before analysis) 15 (41)  
Late (<10 years before analysis) 22 (59)  
Induction   
ATRA + anthracycline + cytarabine and/or hydroxyurea 13 (35)  
ATRA + anthracycline 12 (32)  
ATRA + anthracycline + ATO + cytarabine and/or hydroxyurea 7 (19)  
ATRA + anthracycline + ATO 4 (11)  
ATRA + hydroxyurea 1 (3)  
Consolidation   
ATRA + chemotherapy 14 (50)  
ATRA + ATO 13 (46)  
ATRA + ATO + chemotherapy 1 (4)  
Maintenance   
ATRA + 6MP + MTX 12 (100)  
ATRA + ATO 0 (0)  

ATO, arsenic trioxide; ATRA, all-trans retinoic acid; FISH, fluorescence in situ hybridization; ITD, internal tandem duplication; MTX, methotrexate; TKD, tyrosine kinase domain mutation; 6MP, 6-mercaptopurine.

The median D-dimer is an approximation only and can be regarded as a minimum figure because some laboratories quoted results as greater than a particular threshold rather than providing a specific figure.

Sites of bleeding were intracranial (10, including intracerebral, subdural and subarachnoid), cutaneous (9, including bruising and bleeding from puncture sites), mucosal (7, including epistaxis, gastrointestinal, and urinary tract), intraocular or peri-orbital bleeding (3), intrapulmonary (1), and site not specified (1).

Sites of thromboses included intracerebral (3), deep venous thrombosis (1), superficial venous thrombosis (1), hepatic vein (1), pulmonary embolism (2), subclavian artery (1), and digital necrosis (1).

or Create an Account

Close Modal
Close Modal