Table 3.

Comparison of testing and validation cohort

Testing, n = 80Validation, n = 30P
Initial presentation    
 Female, n (%) 50 (63) 17 (57) .66 
 PVT, n (%) 52 (65) 25 (83) .07 
 Age at diagnosis, mean (range), y 42 (17-73) 47 (7-76) .16 
 Hemoglobin, median (range), g/dL* 14.2 (8.6-19.5) 13 (9.2-21.6) .94 
 Platelet count, median (range), ×109/L* 340 (136-2103) 339 (156-1700) .82 
 WBC count, median (range), ×109/L* 8.6 (3.5-34.9) 8 (3-14) .42 
 Spleen size BCM, median (range), cm 2 (0-9) 1.5 (0-10) .76 
MPN subtype and driver mutation, n (%)    
  PV 52 (65) 12 (40) .04 
  ET 23 (29) 13 (43) .04 
  PMF 5 (6) 5 (17) .04 
JAK2 V617F/CALR/MPL, n 76/4/0 29/0/1 .20 
JAK2 allele burden, median (range), % 14.5 (0.4-93) 30 (4-99) .33 
JAK2 allele burden ≥50%, n (%) 16 (21) 4 (13) .58 
Additional mutation, n (%) 37 (46) 9 (30) .14 
High-risk score, n (%) 23 (29) 8 (27) 1.00 
Treatment and outcomes    
 Follow-up, median (range), y 11 (0.3-37) 7 (0.3-39) .34 
 Cytoreductive treatment, n (%) 75 (94) 30 (100) .32 
Primary outcomes, n (%) 10 (13) 9 (30) .05 
 Secondary myelofibrosis 7 (9) 7 (28) .04 
 Acute leukemia 2 (3) 2 (7) .30 
 Death 5 (6) 4 (13) .25 
Thrombosis, n (%)    
 Thrombophilia 14 (18) 3 (10) .39 
 Anticoagulant therapy 78 (97) 27 (90) .13 
 Thrombosis recurrence 12 (15) 8 (27) .17 
Testing, n = 80Validation, n = 30P
Initial presentation    
 Female, n (%) 50 (63) 17 (57) .66 
 PVT, n (%) 52 (65) 25 (83) .07 
 Age at diagnosis, mean (range), y 42 (17-73) 47 (7-76) .16 
 Hemoglobin, median (range), g/dL* 14.2 (8.6-19.5) 13 (9.2-21.6) .94 
 Platelet count, median (range), ×109/L* 340 (136-2103) 339 (156-1700) .82 
 WBC count, median (range), ×109/L* 8.6 (3.5-34.9) 8 (3-14) .42 
 Spleen size BCM, median (range), cm 2 (0-9) 1.5 (0-10) .76 
MPN subtype and driver mutation, n (%)    
  PV 52 (65) 12 (40) .04 
  ET 23 (29) 13 (43) .04 
  PMF 5 (6) 5 (17) .04 
JAK2 V617F/CALR/MPL, n 76/4/0 29/0/1 .20 
JAK2 allele burden, median (range), % 14.5 (0.4-93) 30 (4-99) .33 
JAK2 allele burden ≥50%, n (%) 16 (21) 4 (13) .58 
Additional mutation, n (%) 37 (46) 9 (30) .14 
High-risk score, n (%) 23 (29) 8 (27) 1.00 
Treatment and outcomes    
 Follow-up, median (range), y 11 (0.3-37) 7 (0.3-39) .34 
 Cytoreductive treatment, n (%) 75 (94) 30 (100) .32 
Primary outcomes, n (%) 10 (13) 9 (30) .05 
 Secondary myelofibrosis 7 (9) 7 (28) .04 
 Acute leukemia 2 (3) 2 (7) .30 
 Death 5 (6) 4 (13) .25 
Thrombosis, n (%)    
 Thrombophilia 14 (18) 3 (10) .39 
 Anticoagulant therapy 78 (97) 27 (90) .13 
 Thrombosis recurrence 12 (15) 8 (27) .17 
*

Missing data for 8 and 6 patients in initial and validation cohort, respectively.

Missing data for 16 and 7 patients in initial and validation cohort, respectively.

Death related to refractory acute leukemia (n = 2), nonrelapse mortality after allogeneic hematopoietic stem cell transplantation (n = 1), and sudden cardiac arrest (n = 1).

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