Table 1 Clinical data of 937 PV and ET patients.

From: QRISK3 score is predictive of thrombotic risk in patients with myeloproliferative neoplasms

 

ET patients (490) [range] – (%)

PV patients (447) [range] – (%)

Sex, male/female

145/345 (26/74)

214/233 (48/52)

Age at diagnosis, years

47 [25–85]

46 [25–84]

Mutational status:

Available for 424

Available for 420

 JAK2

253 (59.7)

405 (96.4)

 MPL

7 (1.6)

/

 CALR

117 (27.6)

/

 Triple-negative

47 (11.1)

15 (3.6)

VAF, %

Available for 34

13 [1–41] % a

Available for 39

39 [7–98] %**

Risk at diagnosis

 Low

355 (72.4)

312 (69.8)

 High

135 (27.5)

135 (31.2)

QRISK3 score at diagnosis

3.2 [0.1–40.6] %

3.5 [0.1–41] %

Primary MPN-specific approach*

 Watch and wait/venesection

292 (59.5)

276 (61.7)

 Hydroxyurea

143 (29.2)

106 (23.7)

 Ruxolitinib

11 (2.3)

10 (2.2)

 Interferon-α

44 (9)

55 (12.4)

Thrombosis history at/before diagnosis

64 (13.1)

84 (18.8)

Thrombosis during follow-up

 Events

52 events in 46 patients (9.4)

73 events in 62 patients (13.9)

 Time to thrombosis, months

39 [2–324]

38 [1–232]

Thrombosis site:

 Pulmonary embolism

2 (3.8)

5 (6.8)

 Myocardial infarction

8 (15.4)

16 (21.9)

 Cerebrovascular accident

14 (26.9)

27 (37.1)

 Portal vein

4 (7.7)

5 (6.8)

 Other VTE

23 (44.3)

20 (27.4)

 Other arterial

1 (1.9)

/

Transformed to PET/PPV MF

9 (1.8)

9 (2)

Status:

 Alive

389 (79.4)

382 (85.4)

 Death

25 (5.1)

16 (3.6)

 Lost at follow-up

76 (15.5)

49 (11)

Median follow-up, months

85 [3–481]

95 [3–405]

  1. PET post ET, PPV post PV; MF myelofibrosis.
  2. *therapy used from diagnosis or for longest time period if different.
  3. NA not available, VTE venous thromboembolism.