Details on patient characteristics and transplantation procedure
Item and specification . | n . | % . |
---|---|---|
Patients | 70 | 100 |
Sex | ||
Male | 44 | 63 |
Female | 26 | 37 |
Malformations | ||
No | 20 | 34 |
Yes | 38 | 66 |
Facial dysmorphia | 24 | |
Skeletal malformations | 13 | |
Heart defects | 18 | |
Renal/urogenital malformations | 7 | |
Other | 10 | |
Missing | 12 | |
Molecular genetics | ||
RPS19 | 18 | 40 |
RPL5 | 6 | 13 |
RPS26 | 5 | 11 |
RPL11 | 3 | 7 |
RPL35A | 1 | 2 |
RPS17 | 1 | 2 |
Negative | 11 | 24 |
Missing | 25 | |
Steroid trial | ||
Yes | 52 | 96 |
No | 2 | 4 |
Missing | 16 | |
Number of transfusions | ||
<20 | 10 | 19 |
20-50 | 22 | 41 |
>50 | 22 | 41 |
Missing | 16 | |
Chelation | ||
Yes | 41 | 75 |
No | 14 | 26 |
Missing | 15 | |
Ferritin prior to HSCT | ||
<1000 µg/L | 12 | 24 |
≥1000 µg/L | 39 | 77 |
Missing | 19 | |
Indication for HSCT | ||
Transfusion dependency | 56 | 95 |
+ Additional cytopenia | 12 | |
+ Deferoxamine toxicity | 2 | |
+ Alloimmunization | 1 | |
Steroid dependency | 1 | 2 |
Steroid side effects | 1 | 2 |
Secondary MDS | 1 | 2 |
Missing | 11 | |
Year of HSCT | ||
<2000 | 19 | 27 |
≥2000 | 51 | 73 |
Age at HSCT, y* | ||
<10 | 52 | 74 |
0-18 | 18 | 26 |
Donor | ||
MSD | 45 | 64 |
MUD (10/10) | 12 | 17 |
UD (9/10) | 7 | 10 |
UD other (HLA 8/8, 8/10, 6/6, and ND) | 6 | 9 |
Stem cell source | ||
BM | 56 | 80 |
PBSCs | 7 | 10 |
CB (siblings) | 7 | 10 |
Conditioning regimen | ||
Bu/cyclophosphamide | 35 | 50 |
Bu/other | 13 | 19 |
Treo/thiotepa/fludarabine | 13 | 19 |
TBI based | 3 | 4 |
Other | 6 | 9 |
ATG/ALG | ||
Yes | 57 | 81 |
No | 13 | 19 |
GVHD prophylaxis | ||
MSD: ATG/CSA/MTX (MMF†) | 22 | 49 |
ATG/CSA | 11 | 24 |
CSA/ MTX (MMF†) | 7 | 7 |
CSA | 4 | 16 |
MTX long course | 1 | 1 |
UD: ATG/CSA/MTX‡ | 18 | 72 |
ATG/CSA | 4 | 16 |
CSA/MTX/anti-rIL-2 | 1 | 4 |
None§ | 2 | 8 |
Item and specification . | n . | % . |
---|---|---|
Patients | 70 | 100 |
Sex | ||
Male | 44 | 63 |
Female | 26 | 37 |
Malformations | ||
No | 20 | 34 |
Yes | 38 | 66 |
Facial dysmorphia | 24 | |
Skeletal malformations | 13 | |
Heart defects | 18 | |
Renal/urogenital malformations | 7 | |
Other | 10 | |
Missing | 12 | |
Molecular genetics | ||
RPS19 | 18 | 40 |
RPL5 | 6 | 13 |
RPS26 | 5 | 11 |
RPL11 | 3 | 7 |
RPL35A | 1 | 2 |
RPS17 | 1 | 2 |
Negative | 11 | 24 |
Missing | 25 | |
Steroid trial | ||
Yes | 52 | 96 |
No | 2 | 4 |
Missing | 16 | |
Number of transfusions | ||
<20 | 10 | 19 |
20-50 | 22 | 41 |
>50 | 22 | 41 |
Missing | 16 | |
Chelation | ||
Yes | 41 | 75 |
No | 14 | 26 |
Missing | 15 | |
Ferritin prior to HSCT | ||
<1000 µg/L | 12 | 24 |
≥1000 µg/L | 39 | 77 |
Missing | 19 | |
Indication for HSCT | ||
Transfusion dependency | 56 | 95 |
+ Additional cytopenia | 12 | |
+ Deferoxamine toxicity | 2 | |
+ Alloimmunization | 1 | |
Steroid dependency | 1 | 2 |
Steroid side effects | 1 | 2 |
Secondary MDS | 1 | 2 |
Missing | 11 | |
Year of HSCT | ||
<2000 | 19 | 27 |
≥2000 | 51 | 73 |
Age at HSCT, y* | ||
<10 | 52 | 74 |
0-18 | 18 | 26 |
Donor | ||
MSD | 45 | 64 |
MUD (10/10) | 12 | 17 |
UD (9/10) | 7 | 10 |
UD other (HLA 8/8, 8/10, 6/6, and ND) | 6 | 9 |
Stem cell source | ||
BM | 56 | 80 |
PBSCs | 7 | 10 |
CB (siblings) | 7 | 10 |
Conditioning regimen | ||
Bu/cyclophosphamide | 35 | 50 |
Bu/other | 13 | 19 |
Treo/thiotepa/fludarabine | 13 | 19 |
TBI based | 3 | 4 |
Other | 6 | 9 |
ATG/ALG | ||
Yes | 57 | 81 |
No | 13 | 19 |
GVHD prophylaxis | ||
MSD: ATG/CSA/MTX (MMF†) | 22 | 49 |
ATG/CSA | 11 | 24 |
CSA/ MTX (MMF†) | 7 | 7 |
CSA | 4 | 16 |
MTX long course | 1 | 1 |
UD: ATG/CSA/MTX‡ | 18 | 72 |
ATG/CSA | 4 | 16 |
CSA/MTX/anti-rIL-2 | 1 | 4 |
None§ | 2 | 8 |
Anti-rIL2, anti-interleukin-2 receptor antibody; ATG/ALG, antithymocyte/lymphocyte globulin; BM, bone marrow; Bu, busulfan; CB, cord blood; CSA, cyclosporine A; Cy, cyclophosphamide; MMF, mycophenolate mofetil; MTX, methotrexate; MUD, matched unrelated donor; ND, no data; PBSCs, peripheral blood stem cells; TBI, total body irradiation; Treo, treosulfan.
Median 5.5 years (range, 0.9-17.3 years).
MTX was replaced by MMF in 1 patient.
Including 1 patient receiving a CD3/CD19-depleted graft.
Including 1 patient each with a CD3/CD19-depleted and CD34+ selected graft.