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. 2006 May 23;108(9):2928–2936. doi: 10.1182/blood-2006-03-008706

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

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.