Skip to main content
. 2015 Dec 3;8(1):29–39. doi: 10.14740/jocmr2405w

Table 3. Clinical and Laboratory Features of PMF Patients Divided by IDH Mutational Status.

PMF IDH mutant (mean (SD)) IDH wild-type (mean (SD)) P value
Number of patients 5 72 -
Age at recording 64.2 (20) 60.6 (14.2) 0.642
Age at diagnosis 55.4 (20.6) 56.93 (14.1) 0.86
Age at sampling 63.2 (20.1) 59.3 (14.02) 0.679
Females (%) 5 (100%) 38 (52.8%) 0.063
Total leukocyte at diagnosis (mm3) 9.662 (5.725) 14.892 (13.886) 0.482
Hb at diagnosis (g/dL) 10 (1.3) 10.6 (2.2) 0.482
HCT at diagnosis (%) 31.4 (4.87) 32.1 (7.13) 0.694
Platelet count at diagnosis (mm3) 272.760 (267.777) 444.948 (366.701) 0.193
LDH at diagnosis (U/L) 713 (470) 836 (390) 0.251
Spleen size at diagnosis (mm) 179.4 (30.7) 198.9 (43.7) 0.325
PMF IDH mutant, n (%) IDH wild-type, n (%) P value
Risk factors for cardiovascular diseases 3 (60%) 43 (59.7%) 1
Splenomegaly group 5 (100%) 72 (100%) 0.594
  No splenomegaly 0 1 (1.4%) -
  Mild splenomegaly 2 (40%) 15 (20.8%) -
  Massive splenomegaly 3 (60%) 56 (77.8%) -
Bleeding 3 (60%) 12 (16.7%) 0.048
Need for red blood cell transfusion 1 (20%) 20 (27.8%) 1
Hydroxyurea 5 (100%) 67 (93.1%) 1
History of splenectomy 0 4 (5.6%) 1
AHSCT 0 3 (4.2%) 1
ASA 1 (20%) 46 (63.9%) 0.072
Leukemic transformation 1 (20%) 3 (4.2%) 0.24
Death 3 (60%) 11 (15.3%) 0.039
Thrombosis 1 (20%) 10 (13.9%) 0.548
Thrombosis group 5 (100%) 72 (100%) 0.802
  No thrombosis 4 (80%) 62 (86.1%) -
  Arterial 1 (20%) 6 (8.3%) -
  Venous 0 3 (4.2%) -
  Arterial and venous 0 1 (1.4%) -
JAK2V617F mutation 3 (60%) 55 (76.4%) 0.592
JAK2V617F group 5 (100%) 72 (100%) 0.401
  No mutation 2 (40%) 17 (23.6%) -
  Low allele burden 3 (60%) 37 (51.4%) -
  High allele burden 0 18 (25%) -
Karyotype 5 (100%) 72 (100%) 0.671
  Normal 5 (100%) 62 (86.1%) -
  Favorable 0 7 (9.7%) -
  Unfavorable 0 3 (4.2%) -
DIPSS-plus 5 (100%) 72 (100%) 0.889
  Low risk 1 (20%) 14 (19.4%) -
  Intermediate-1 risk 2 (40%) 25 (34.7%) -
  Intermediate-2 risk 2 (40%) 25 (34.7%) -
  High risk 0 8 (11.2%) -