Table 1.

Patient characteristics and overall transplantation outcome




All patients

RIC

Conventional

P
No. patients   129   57   72   
Median age, y (range)   42 (5-72)   50 (5-72)   37 (8-64)   .02  
Male sex, no. (%)  78 (60)   33 (58)   45 (62)   
    Female donor, no. (%)   43 (33)   21 (37)   22 (31)   
Patient CMV seropositive (IgG), no. (%)  79 (61)   35 (61)   44 (61)   
    Seronegative donors, no. (%)   29 (33)   17 (30)   12 (17)   
Underlying disease, no. (%)     
    Acute leukemia or myelodysplasia   107 (83)   46 (81)   61 (85)   
    Chronic myelogenous leukemia   5 (4)   3 (5)   2 (3)   
    Lymphoma   8 (6)   6 (10)   2 (3)   
    Multiple myeloma or CLL   3 (2)   1 (2)   2 (3)   
    Other   6 (5)   1 (2)   5 (7)   
Disease status at transplantation, no. (%)*     
    Early   44 (34)   20 (35)   24 (33)   
    Advanced   85 (66)   37 (65)   48 (67)   
Prior autologous HSCT, no. (%)   10 (8)   6 (11)   4 (6)   
Donor type, no. (%)     
    HLA-identical sibling   71 (55)   28 (50)   43 (60)   
    Alternative (VUD/family mismatched)   58   29   29   
Stem cell source, no. (%)     
    Peripheral blood   99 (77)   49 (86)   50 (69)   .03  
    Bone marrow   28   8   20   
    Cord blood   2   —   2   
Transplantation year, no. (%)     
    1998-2000   32 (25)   11 (19)   21 (29)   
    2001-2004   97 (75)   46 (81)   51 (71)   
ATG or alemtuzumab in conditioning, no. (%)   60 (47)   34 (60)   26 (36)   < .01  
Ex vivo T-cell depletion, no. (%)   22 (17)   16 (28)   6 (8)   .04  
Conditioning regimen, no. (%)     
    TBI-based conventional myeloablative therapy   —   —   49 (68)   
    Chemotherapy-only conventional myeloablative therapy   —   —   23 (32)   
Reduced-intensity therapy     
    Alkylating agent(s) + fludarabine   —   48 (84)   —   
    Low-dose TBI (≤ 4 Gy) + fludarabine   —   9 (16)   —   
GVHD prophylaxis, no. (%)     .04  
    CsA ± steroids ± ATG   36 (28)   22 (39)   14 (19)   
    CsA or Tacro + MTX ± ATG   77 (60)   21 (37)   56 (78)   
    CsA or Tacro + MMF ± ATG   16 (12)   14 (25)   2 (3)   
Median d of neutropenia (range)  18 (1-123)   10 (1-123)   19 (8-93)   .03  
    Less than 7 d of neutropenia, no. (%)   20 (16)   14 (25)   6 (8)   .02  
    Less than 21 d of neutropenia, no. (%)   81 (63)   41 (72)   40 (56)   
Stable donor engraftment, no. (%)   118 (91)   56 (97)   62 (87)   .04  
No. developing grades II-IV aGVHD (% CumInc, 95% CI)   53 (36, 28-44)   17 (26, 14-38)   36 (44, 32-56)   .03  
No. developed cGVHD (% CumInc, 95% CI)   45 (30, 18-42)   24 (34, 20-48)   21 (26, 16-36)   
2-y nonrelapse mortality, % CumInc (95% CI)   30 (19-39)   29 (18-48)   30 (19-39)   
2-y disease relapse, % CumInc (95% CI)   33 (19-45)   32 (13-45)   35 (20-50)   
Overall survival, % CumInc (95% CI)   42 (30-50)   42 (24-52)   42 (25-53)   
Median d follow-up (range)
 
287 (2-1414)
 
253 (2-1326)
 
365 (7-1414)
 
.1
 



All patients

RIC

Conventional

P
No. patients   129   57   72   
Median age, y (range)   42 (5-72)   50 (5-72)   37 (8-64)   .02  
Male sex, no. (%)  78 (60)   33 (58)   45 (62)   
    Female donor, no. (%)   43 (33)   21 (37)   22 (31)   
Patient CMV seropositive (IgG), no. (%)  79 (61)   35 (61)   44 (61)   
    Seronegative donors, no. (%)   29 (33)   17 (30)   12 (17)   
Underlying disease, no. (%)     
    Acute leukemia or myelodysplasia   107 (83)   46 (81)   61 (85)   
    Chronic myelogenous leukemia   5 (4)   3 (5)   2 (3)   
    Lymphoma   8 (6)   6 (10)   2 (3)   
    Multiple myeloma or CLL   3 (2)   1 (2)   2 (3)   
    Other   6 (5)   1 (2)   5 (7)   
Disease status at transplantation, no. (%)*     
    Early   44 (34)   20 (35)   24 (33)   
    Advanced   85 (66)   37 (65)   48 (67)   
Prior autologous HSCT, no. (%)   10 (8)   6 (11)   4 (6)   
Donor type, no. (%)     
    HLA-identical sibling   71 (55)   28 (50)   43 (60)   
    Alternative (VUD/family mismatched)   58   29   29   
Stem cell source, no. (%)     
    Peripheral blood   99 (77)   49 (86)   50 (69)   .03  
    Bone marrow   28   8   20   
    Cord blood   2   —   2   
Transplantation year, no. (%)     
    1998-2000   32 (25)   11 (19)   21 (29)   
    2001-2004   97 (75)   46 (81)   51 (71)   
ATG or alemtuzumab in conditioning, no. (%)   60 (47)   34 (60)   26 (36)   < .01  
Ex vivo T-cell depletion, no. (%)   22 (17)   16 (28)   6 (8)   .04  
Conditioning regimen, no. (%)     
    TBI-based conventional myeloablative therapy   —   —   49 (68)   
    Chemotherapy-only conventional myeloablative therapy   —   —   23 (32)   
Reduced-intensity therapy     
    Alkylating agent(s) + fludarabine   —   48 (84)   —   
    Low-dose TBI (≤ 4 Gy) + fludarabine   —   9 (16)   —   
GVHD prophylaxis, no. (%)     .04  
    CsA ± steroids ± ATG   36 (28)   22 (39)   14 (19)   
    CsA or Tacro + MTX ± ATG   77 (60)   21 (37)   56 (78)   
    CsA or Tacro + MMF ± ATG   16 (12)   14 (25)   2 (3)   
Median d of neutropenia (range)  18 (1-123)   10 (1-123)   19 (8-93)   .03  
    Less than 7 d of neutropenia, no. (%)   20 (16)   14 (25)   6 (8)   .02  
    Less than 21 d of neutropenia, no. (%)   81 (63)   41 (72)   40 (56)   
Stable donor engraftment, no. (%)   118 (91)   56 (97)   62 (87)   .04  
No. developing grades II-IV aGVHD (% CumInc, 95% CI)   53 (36, 28-44)   17 (26, 14-38)   36 (44, 32-56)   .03  
No. developed cGVHD (% CumInc, 95% CI)   45 (30, 18-42)   24 (34, 20-48)   21 (26, 16-36)   
2-y nonrelapse mortality, % CumInc (95% CI)   30 (19-39)   29 (18-48)   30 (19-39)   
2-y disease relapse, % CumInc (95% CI)   33 (19-45)   32 (13-45)   35 (20-50)   
Overall survival, % CumInc (95% CI)   42 (30-50)   42 (24-52)   42 (25-53)   
Median d follow-up (range)
 
287 (2-1414)
 
253 (2-1326)
 
365 (7-1414)
 
.1
 

CLL indicates chronic lymphocytic leukemia; VUD, volunteer unrelated donor; CsA, cyclosporine A; MTX, methotrexate; MMF, mycophenolate mofetil; Tacro, tacrolimus; and —, not applicable.

*

Early indicates acute leukemia and myelodysplastic syndrome in first complete remission after chemotherapy (< 5% blasts), previously untreated low-risk MDS, and chronic myeloid leukemia in first chronic phase; advanced, malignancies in a phase beyond the early phase, and multiple myeloma, CLL, and non-Hodgkin lymphoma, Hodgkin disease, and solid tumors.

Neutropenia is defined as < 0.5 × 109 cells/L.

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