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Table 2 Molecular and clinical characteristics of patients with primary myelofibrosis (PMF)

From: A distinct molecular mutational profile and its clinical impact in essential thrombocythemia and primary myelofibrosis patients

Variables

CALR mutation (n = 19)

JAK2 mutation (n = 23)

Triple Negative (n = 3)

p-value

Males (%)

13 (68.4)

14 (60.9)

1 (33.3)

0.025*

Age,

Median (Range)

45 (37–70)

53 (21–76)

43 (22–60)

0.138

Haemoglobin (g/dL),

Median (Range)

10.5 (9.5–13.4)

9.8 (6.6–15)

7.9 (6.5–14.2)

0.45

TLC ×109/L,

Median (Range)

9.8 (5.6–63.2)

11.9 (1.8–22.1)

40.9 (15.1–25)

0.075

Platelet × 109/L,

Median (Range)

273 (122–1147)

382.5 (12–239)

131.5 (38–483)

0.358

Circulating blasts (%),

Median (Range)

29

47.5 (44–51)

38

0.306

Reticulin Fibrosis

MF 0

0

0

0

 

MF 1

5 (26.3)

15 (65.2)

2 (66.7)

0.067

MF 2

14 (73.7)

8 (34.8)

1 (33.3)

 

Constitutional symptoms (%)

12 (63.2)

14 (60.9)

3 (100)

0.421

DIPSS score, (%):

 Low

4 (21.1)

0

0

 

 Intermediate-1

2 (10.5)

5 (21.7)

0

0.259

 Intermediate-2

9 (47.4)

15 (65.2)

3 (100)

 

 High

4 (21.1)

3 (13)

0

 

Leukemic transformation, (%)

2 (10.5)

2 (8.7)

1 (33.3)

0.629

  1. *significant