Table 1.
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).