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Table 1 The patients’ characteristics at diagnosis according to myelofibrosis (n = 316)

From: Allogeneic stem cell transplantation may overcome the adverse impact of myelofibrosis on the prognosis of myelodysplastic syndrome

 

MF = 0/1 (n = 273)

MF = 2/3 (n = 43)

P

Age (years), median, range

52 (14–83)

52 (21–79)

0.705

Gender, no. (%)

 Male

181 (66.3%)

27 (62.8%)

0.652

 Female

92 (33.7%)

16 (37.2%)

 

Median WBC (range), × 109/L

2.66 (0.27–13.47)

2.73 (1.10–12.00)

0.609

Median NE (range), × 109/L

0.99 (0.02–11.34)

0.85 (0.04–4.92)

0.794

Median HGB (range), g/L

69 (26–150)

67 (30–138)

0.291

Median PLT (range), × 109/L

53 (1–408)

47 (3–282)

0.911

MDS subtypes (WHO, 2016), no. (%)

0.243

 MDS-SLD

11 (4.0%)

2 (4.7%)

 

 MDS-MLD

52 (19.1%)

4 (9.3%)

 

 MDS-RS-SLD

2 (0.7%)

2 (4.7%)

 

 MDS-RS-MLD

8 (2.9%)

3 (7.0%)

 

 MDS with isolated 5q-deletion

2 (0.7%)

0 (0.0%)

 

 MDS-EB-1

70 (25.7%)

10 (23.2%)

 

 MDS-EB-2

118 (43.2%)

21 (48.8%)

 

 MDS-U

10 (3.7%)

1 (2.3%)

 

Cytogenetic

0.001

 Normal karyotype

148 (54.2%)

12 (27.9%)

 

 Aberrant karyotype

125 (45.8%)

31 (72.1%)

 

IPSS-R risk group, no. (%)

0.859

 Very low

4 (1.5%)

0 (0.0%)

 

 Low

29 (10.6%)

5 (11.6%)

 

 Intermediate

65 (23.8%)

9 (20.9%)

 

 High

84 (30.8%)

12 (27.9%)

 

 Very high

91 (33.3%)

17 (39.6%)

 

Treatment, no. (%)

0.170

 Allogeneic HSCT

121 (44.3%)

20 (46.5%)

 

 Cytoreductive treatments without HSCT

90 (33.0%)

12 (27.9%)

 

  HMA

68 (25.0%)

10 (23.2%)

 

  Chemotherapy combined with HMA

20 (7.3%)

2 (4.7%)

 

  AML-like chemotherapy

2 (0.7%)

0 (0.0%)

 

 Immunoregulatory

11 (4.0%)

5 (11.6%)

 

 Supportive care

51 (18.7%)

6 (14.0%)

 

Leukemia transformation, no. (%)

50 (18.3%)

8 (18.6%)

0.964

Median time from diagnosis to leukemia transformation, months (range)

12 (2–31)

7 (1–20)

0.043

  1. MF myelofibrosis, WBC white blood cell count, NE neutrophils, HGB hemoglobin, PLT platelet, MDS-SLD MDS with single-lineage dysplasia, MDS-MLD MDS with ring sideroblasts with multilineage dysplasia, MDS-RS-SLD MDS with ring sideroblasts with single-lineage dysplasia, MDS-RS-MLD MDS with ring sideroblasts with multilineage dysplasia, MDS-EB MDS with excess of blasts, MDS-U MDS unclassifiable, HSCT hematopoietic stem cell transplantation, HMA hypomethylating agents, AML acute myeloid leukemia