Table 4.
Parameters | Study |
|||
---|---|---|---|---|
Collins et al.[8] | Schmidt et al.[10] | Levine et al.[9] | Current | |
Design | Retrospective | Retrospective | Prospective | Prospective |
Disease, no. of patients | ||||
Acute myeloid leukemia | 7* | 124* | 50* | 11 |
Acute lymphoblastic leukemia | 3* | 0 | 0 | 6 |
DLI dose, ×108/kg CD3 | 2.2 (mean)† | 0.1 (median)‡ | 1 | 1 |
Grades II–IV acute GVHD | 46%† | 34%‡ | 45%§ | 35% |
Grades III–IV acute GVHD | 22%† | NA | 28%§ | 29% |
Chronic GVHD | 61%† | 46%‡ | 36%§ | 64% |
Chronic extensive GVHD | 32%† | 26%‡ | 14%§ | 50% |
1 year DFS after DLI | 54% in AML 33% in ALL |
NA | 34% among patients in CR at DLI§ | 40% in AML CR at DLI, 8.3% in others |
DLI indicates donor lymphocyte infusion; GVHD, graft-versus-host disease; NA, not assessable; DFS, disease-free survival; AML, acute myeloid leukemia; ALL, acute lymphoblastic leukemia; CR, complete remission.
Data abstracted from the entire cohort.
Data represent the entire study cohort of 140 patients treated for various diagnoses and irrespective of the presence of chemotherapy before DLI.
Data represent the entire study cohort of 171 AML patients. Of the 171 patients, 124 received chemotherapy before DLI and information was missing in 7 patients.
Data represent the entire study cohort of 65 patients including 50 with AML and 15 with other diagnoses.