Table 1 Patient, disease and transplant characteristics.

From: The number of additional high molecular risk mutations predicts outcome after hematopoietic stem cell transplantation in primary and secondary myelofibrosis

Characteristics at transplant

All, n = 50 (%)

Median age, years (range)

58.5 (36–67)

Sex, N(%)

 Female

14 (28)

 Males

36 (72)

Myelofibrosis, N(%)

 Primary

17 (34)

 Secondary to PV/ET

33 (66)

  ET

21

  PV

12

Anemia (Hb <10 g/dl)

34 (68)

Severe anemia (Hb < 8 g/dl)

9 (18)

Thrombocytopenia

 Moderate (<100.000/mcl)

11 (22)

 Severe (<50.000/mcl)

7 (14)

Driver.mutations

CALR

14 (28)

JAK2

26 (52)

MPL

6 (12)

 Triple negative

4 (8)

Bone marrow fibrosis grade

 1

4 (8.2)

 2

21 (42.9)

 3

24 (49)

ECOG.PS

 0

18 (36)

 1

29 (58)

 2

3 (6)

HCT-CI

 0

12 (24)

 1–2

21 (42)

 >2

17 (34)

Splanchnic vein thrombosis

12 (24)

Spleen size ≥22 cm

12 (24)

Splenectomy

10 (20)

Karnofsky ≤70

3 (6)

Trasfusion.dependent.before transplant

24 (48)

Ruxolinitib o Fedratinib before transplant

26 (52)

Cytogenetic

 Favorable abnormality

4 (8.7)

 Normal karyotype

29 (63)

 Other abnormalities

7 (15.2)

 Very high-risk abnormalities

6 (12)

Time from diagnosis to transplant (years), median (range)

2.4 (0.2–15.1)

Donor

 Sibling

10 (20)

 Haploidentical

6 (12)

 Matched unrelated donor

26 (52)

 Mismatched unrelated donor

8 (16)

Source of stem cells

 Bone marrow

2 (4)

 Peripheral blood

48 (96)

Conditioning regimen

 Bu + Flu

12 (24)

 Flu + Mel

5 (10)

 Flu + Thiotepa

3 (6)

 Thiotepa + Bu + Flu

30 (60)

ATG yes

37 (74)

Conditioning intensity

 RIC

48 (96)

 MAC

2 (4)