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. Author manuscript; available in PMC: 2012 Nov 1.
Published in final edited form as: Biol Blood Marrow Transplant. 2011 Jul 30;17(11):1594–1601. doi: 10.1016/j.bbmt.2011.07.021

Table 1.

Characteristics of 401 patients with acute GVHD grades II–IV after reduced-intensity allogeneic HCT.

Age at HCT, years
 Median (range) 55 (<1–75)

Gender
 Male 254 (63%)
 Female 147 (37%)

Donor
 Related donor 164 (41%)
 Unrelated donor 237 (59%)
  HLA-matched 173
  HLA-mismatched 64

Transplant indication
 Acute myeloid leukemia 104
 Non-Hodgkin lymphoma 77
 Multiple myeloma 56
 Chronic lymphocytic leukemia 39
 Myelodysplastic syndrome 25
 Primary ID/marrow failure 25
 Acute lymphoblastic leukemia 24
 Hodgkin lymphoma 23
 Chronic myelogenous leukemia 11
 Aplastic anemia 7
 Solid tumor 6
 Myeloproliferative disorder 4

Conditioning regimen
 2 Gy TBI 51
 2 Gy TBI + fludarabine 90 mg/m2 320
 3 Gy TBI + fludarabine 90 mg/m2 14
 4 Gy TBI + fludarabine 90 mg/m2 7
 CY 200 mg/kg + hATG 90 mg/kg 8
 No conditioning 1

Stem cell source
 G-PBMC 370 (92%)
 Bone marrow 31 (8%)

CD34+ cell dose, cells/kg
 Median 7.82 × 106

Median time to acute GVHD onset 35 days

Peak acute GVHD grade
 II 325 (81%)
 III–IV 76 (19%)

Abbreviations: HCT, hematopoietic cell transplantation; HLA, human leukocyte antigen; ID, immunodeficiency; TBI, total body irradiation; CY, cyclophosphamide; hATG, horse antithymocyte globulin; G-PBMC, granulocyte colony-stimulating factor-mobilized peripheral blood mononuclear cells; acute GVHD, acute graft-vs.-host disease.