Table 1

Characteristics of the 427 patients

No.
Male:female 255:172 
Median age, y (range) 31 (0-66) 
Underlying disease, no. (%)  
    Lymphoma, multiple myeloma 196 (46) 
    Acute leukemia, myelodysplasia, PNH 136 (32) 
    Myeloproliferative disease 56 (13) 
    Other 39 (9) 
Advanced underlying disease,* no. (%) 315/415 (76) 
Type of HSC transplantation, no. (%)  
    Autologous/syngeneic 181 (42) 
    Allogeneic, myeloablative 208 (49) 
    Allogeneic, nonmyeloablative 38 (9) 
Type of donor and HLA status, no. (%)  
    HLA-compatible sibling 187/246 (76) 
    HLA-compatible unrelated 28/246 (11) 
    HLA-mismatched unrelated 33/246 (13) 
Conditioning regimen, no. (%)  
    Busulfan based 119 (28) 
    TBI based 85 (20) 
    Other 223 (52) 
Stem cell source, no. (%)  
    Peripheral blood 225 (53) 
    Bone marrow 168 (39) 
    Cord blood 34 (8) 
No.
Male:female 255:172 
Median age, y (range) 31 (0-66) 
Underlying disease, no. (%)  
    Lymphoma, multiple myeloma 196 (46) 
    Acute leukemia, myelodysplasia, PNH 136 (32) 
    Myeloproliferative disease 56 (13) 
    Other 39 (9) 
Advanced underlying disease,* no. (%) 315/415 (76) 
Type of HSC transplantation, no. (%)  
    Autologous/syngeneic 181 (42) 
    Allogeneic, myeloablative 208 (49) 
    Allogeneic, nonmyeloablative 38 (9) 
Type of donor and HLA status, no. (%)  
    HLA-compatible sibling 187/246 (76) 
    HLA-compatible unrelated 28/246 (11) 
    HLA-mismatched unrelated 33/246 (13) 
Conditioning regimen, no. (%)  
    Busulfan based 119 (28) 
    TBI based 85 (20) 
    Other 223 (52) 
Stem cell source, no. (%)  
    Peripheral blood 225 (53) 
    Bone marrow 168 (39) 
    Cord blood 34 (8) 

PNH indicates paroxysmal nocturnal hemoglobinuria; HSC, hematopoietic stem cell; HLA, human leukocyte antigen; and TBI, total body irradiation.

*

Not applicable to hereditary disorders such as Fanconi anemia and Wiskott-Aldrich syndrome.

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