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. Author manuscript; available in PMC: 2019 Feb 1.
Published in final edited form as: Biol Blood Marrow Transplant. 2017 Oct 12;24(2):308–313. doi: 10.1016/j.bbmt.2017.10.016

Table 1.

Patient Characteristics

Characteristic N (%) /Median (range)
Patient number 36
Gender (male/female) 31/5
Patient age at HCT, years, median (range) 56 (35–72)
Diagnosis, No.
 Acute myeloid leukemia 13
 Myelodysplastic syndrome 6
 Chronic lymphocytic leukemia 7
 Non Hodgkin lymphoma 4
 Chronic myeloid leukemia 2
 Myeloproliferative disorder 2
 Multiple myeloma 1
Non Hodgkin lymphoma and myelodysplastic syndrome 1
Disease status at time of study intervention
 CR 13
 Not in CR* 23
Donor source
 HLA-matched related 17
 HLA-matched unrelated 18
 1-allele HLA-mismatched unrelated 1
Transplant conditioning intensity
 Nonmyeloablative (fludarabine/TBI) 34
 Myeloablative
  Busulfan/Cyclophosphamide 1
  Fludarabine/TBI/anti-CD45 Ab 1
GVHD prophylaxis after transplant
 MMF/cyclosporine 25
 MMF/cyclosporine/sirolimus 2
 MMF/tacrolimus 6
 MF/tacrolimus/sirolimus 2
 Cyclosporine/methotrexate 1
Acute GVHD before DLI
 None 30
 Grade II-III 6
Time from HCT to DLI
 ≤100 days 21
 >100 days 15
% of donor CD3 chimerism at time of DLI, median (range) 28 (5–47)
*

Evidence of disease: residual lymphadenopathy (n=8), bone marrow morphology (CLL (n=2); myelofybrosis (n=6)), minimal residual disease detected by marrow flow cytometry/cytogenetics/FISH (n=7).