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Table 1 Demographic data for Thal-HSCT patients by donor group: haploidentical and matched-donor

From: No differences in hemostatic and endothelial activations between haploidentical and matched-donor hematopoietic stem cell transplantation in thalassemia disease

 

Type of donor

P-value

Haploidentical

n = 14

Matched-donor

n = 9

Type of thalassemia, n (%)

0.295a

 HbE/β

13 (93)

7 (78)

 

 β major

1 (7)

2 (22)

 

Age at HSCT in years, median (range)

10.6 (2.7–18.9)

8.2 (3.8–20.2)

0.926b

Day after HSCT in days, median (range)

54 (15–331)

87 (35–296)

0.374b

Ferritin in ng/ml, median (IQR)

2972.6

3512.7

0.913b

Hepatomegaly, n (%)

5 (56)

6 (75)

0.147a

Classification, n (%)

 Age < 7 years, no hepatomegaly

0 (0)

0 (0)

 

 Age > 7 years, no hepatomegaly

4 (44)

2 (25)

 

 Age < 7 years, hepatomegaly

0 (0)

2 (25)

 

 Age > 7 years, hepatomegaly

5 (56)

4 (50)

 

Conditioning regimen, n (%)

 Bu + Cy

 

2 (22)

 

 ATG + Flu + Bu

14 (100)

7 (78)

 

Chimerism, n (%)

  

0.412a

 Complete donor

13 (93)

9 (100)

 

 Mixed

1* (7)

  

Veno-occlusive disease, n (%)

2 (14)

3 (33)

0.280a

Graft-versus-host disease, n (%)

 Acute GvHD

   

 Grade I/II

7 (50)

2 (22)

0.171a

 Grade III/IV

 0 (0) 

1 (11)

 

 Chronic GvHD

1 (7)

0 (0)

0.412a

Infection, n (%)

 Bacterial

3 (21)

 0 (0)

0.136a

 Viral

7 (50)

3 (33)

0.431a

  1. IQR interquartile range, GvHD graft versus host disease
  2. Conditioning regimen: ATG Thymoglobulin, Bu busulfan, Cy Cyclophosphamide, Flu fludarabine
  3. *Donor chimerism 76.5%
  4. *All patients in the haploidentical HSCT group received pre-transplant immunosuppression (PTIS), 7 patients who were > 7 years old in the matched-donor HSCT group received PTIS (ref. 7) PTIS consisted of fludarabine 40 mg/m2/day and dexamethasone 25 mg/m2/day
  5. Statistical analysis performed using: a Chi-Square, b Bonferroni