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. 2021 Apr 1;100(9):2339–2350. doi: 10.1007/s00277-021-04494-z

Table 1.

Clinical characteristics at time of first allo-HSCT

Patients Total cohort Day-100 landmark cohort Day-100 landmark and DLI
no DLI preDLI relDLI
Number 342 292 199 42 51
Age [median (range)] 57 (19-79) 57 (19-78) 57 (19-78) 57 (32-75) 56 (22-78)
AML type
De novo 235 (69%) 205 (70%) 135 (68%) 34 (81%) 36 (71%)
sAML/tAMLa 107 (31%) 87 (30%) 64 (32%) 8 (29%) 15 (29%)
Status pre-HSCT
Complete remission 145 (42%) 134 (46%) 95 (48%) 20 (48%) 19 (37%)
CR1 122 111 79 17 15
CR2 or higher 23 23 16 3 4
Active disease 197 (58%) 158 (54%) 104 (52%) 22 (52%) 32 (63%)
PIF 109 84 56 9 19
REL1 40 33 20 6 7
REL2 or higher 2 2 1 1 -
Progression 5 3 3 - -
Untreatedb 41 36 24 6 6
Conditioning
Myeloablative 85 (21%) 75 (26%) 47 (24%) 12 (29%) 16 (31%)
BU/CY-based 54 48 26 8 14
TT/BU/FLU 31 27 21 4 2
Toxicity-reduced 257 (79%) 217 (74%) 152 (76%) 30 (71%) 35 (69%)
FLU/BCNU/MEL 181 153 102 24 27
FLU/TT-based 68 56 50 3 3
Other FLU or TT 8 8 - 3 5
HLA donor-to-recipient
Unrelated matched 191 (56%) 164 (56%) 112 (56%) 23 (55%) 29 (57%)
Unrelated mismatched 70 (20%) 59 (20%) 37 (19%) 7 (17%) 15 (29%)
Sibling matched 72 (21%) 62 (21%) 44 (22%) 11 (26%) 7 (14%)
Sibling mismatched 4 (1%) 3 (1%) 2 (1%) 1 (2%) -
Othersc 5 (1.5%) 4 (1.4%) 4 (2%) - -

aAbbreviations: sAML/tAML secondary or therapy-related AML, CR complete remission, PIF primary induction failure, REL relapse, BU busulfan, CY cyclophosphamide, FLU fludarabine, BCNU carmustine, MEL melphalan, TT thiotepa. bUp-front allo-HSCT predominantly in patients with sAML/tAML (32 of 41, total cohort; 29 of 36, day-100 landmark cohort; 12 of 12, DLI cohorts). cIdentical twins (2); haploidentical (2) or HLA-matched (1) child