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. 2022 Jan 11;6(1):339–357. doi: 10.1182/bloodadvances.2021004916

Table 1.

Patient characteristics

Characteristic Donor and HCT group
Haploidentical Matched sibling 8/8 HLA-MUD 7/8 HLA-MUD UCB
No. of patients 393 1627 1646 230 305
No. of centers 92 206 181 90 79
Median follow-up, mo (range) 24 (3-67) 26 (3-72) 35 (3-74) 35 (3-64) 35 (3-64)
Median recipient age, y (range) 41 (18-74) 42 (18-75) 43 (18-77) 38 (18-70) 37 (18-70)
Karnofsky performance status (%)
 ≥90 233 (59) 1046 (64) 995 (60) 163 (71) 196 (64)
 <90 152 (39) 542 (33) 629 (38) 65 (28) 107 (35)
 Missing 8 (2) 39 (2) 22 (1) 2 (<1) 2 (<1)
No. of male recipients 214 (54) 969 (60) 976 (59) 134 (58) 176 (58)
HCT-CI score
 0 81 (21) 592 (36) 405 (25) 53 (23) 89 (29)
 1 57 (15) 221 (14) 224 (14) 35 (15) 42 (14)
 2 61 (16) 228 (14) 266 (16) 37 (16) 46 (15)
 3+ 194 (49) 552 (34) 745 (45) 104 (45) 125 (41)
 Missing 0 34 (2) 6 (<1) 1 (<1) 3 (<1)
Race/ethnicity*
 Hispanic White 87 (22) 246 (15) 136 (8) 42 (18) 64 (21)
 Non-Hispanic White 170 (43) 846 (52) 1226 (74) 113 (49) 150 (49)
 Black 59 (15) 74 (5) 53 (3) 19 (8) 27 (9)
 Asian 22 (6) 111 (7) 64 (4) 10 (4) 22 (7)
 Other/not specified 55 (14) 350 (22) 167 (10) 46 (20) 42 (14)
Immunophenotype
 T cell 25 (6) 201 (12) 186 (11) 27 (12) 36 (12)
 B cell 330 (84) 1316 (81) 1319 (80) 185 (80) 246 (81)
 Not specified 38 (10) 110 (7) 141 (9) 18 (8) 23 (8)
Cytogenetic risk score
 Normal 91 (23) 320 (20) 335 (20) 52 (23) 63 (21)
 Poor 222 (56) 750 (46) 855 (52) 101 (44) 154 (50)
 Missing/not tested/other 80 (21) 557 (34) 456 (28) 77 (33) 88 (29)
Ph/BCR-ABL1-positive 152 (46) 562 (43) 614 (47) 80 (43) 122 (50)
Remission status
 CR1, MRD positive 112 (28) 513 (32) 509 (31) 58 (25) 78 (26)
 CR1, MRD negative 143 (36) 644 (40) 697 (42) 85 (37) 124 (41)
 CR1, MRD missing 14 (4) 145 (9) 59 (4) 6 (3) 10 (3)
 CR2 105 (27) 296 (18) 334 (20) 62 (27) 74 (24)
 ≥CR3 19 (5) 29 (2) 47 (3) 19 (8) 19 (6)
Time from diagnosis to HCT (CR1 only) (mo)
 0-5 130 (48) 842 (65) 744 (59) 56 (38) 93 (44)
 6-11 115 (43) 388 (30) 463 (37) 81 (54) 102 (48)
 ≥12 24 (9) 72 (6) 58 (5) 12 (8) 17 (8)
Conditioning regimen
 MAC, TBI-based 163 (41) 984 (60) 950 (58) 139 (60) 217 (71)
 MAC, chemotherapy-based 63 (16) 323 (20) 312 (19) 51 (22) 11 (4)
 RIC/NMA 167 (42) 316 (19) 383 (23) 39 (17) 76 (25)
 Missing 0 4 (<1) 1 (<1) 1 (<1) 1 (<1)
Donor/recipient sex
 Female donor/male recipient 82 (21) 415 (26) 244 (15) 42 (18) 161 (53)
 other donor/recipient 311 (79) 1212 (74) 1396 (85) 188 (82) 137 (45)
 Missing 0 0 6 (<1) 0 7 (2)
Donor/recipient CMV serostatus
 +/+ 206 (52) 859 (53) 506 (31) 90 (39) 0
 +/− 31 (8) 144 (9) 197 (12) 25 (11) 0
 −/+ 83 (21) 287 (18) 553 (34) 64 (28) 0
 −/− 72 (18) 306 (19) 382 (23) 50 (22) 0
 UCB–/recipient+ 0 0 0 0 200 (66)
 UCB–/recipient– 0 0 0 0 100 (33)
 Missing 1 (<1) 31 (2) 8 (<1) 1 (<1) 5 (2)
Median donor age, y (range) 35 (10-74) 41 (9-75) 28 (18-60) 31 (19-60) NA
Graft source
 Bone marrow 160 (41) 230 (14) 316 (19) 67 (29)
 Peripheral blood 233 (59) 1397 (86) 1330 (81) 163 (71)
GVHD prophylaxis
 CNI + MTX ± others 0 1107 (68) 1165 (71) 162 (70) 7 (2)
 CNI + MMF ± others 0 236 (15) 191 (12) 18 (8) 265 (87)
 CNI + others 0 118 (7) 141 (9) 13 (6) 6 (2)
 CNI alone 0 66 (4) 58 (4) 5 (2) 14 (5)
 PTCy + CNI ± MMF 393 (100) 75 (5) 73 (4) 29 (13) 2 (<1)
 Other prophylaxis 0 17 (1) 13 (<1) 2 (<1) 10 (3)
 Missing 0 8 (<1) 5 (<1) 1 (<1) 1 (<1)
In vivo T-cell depletion
 Antithymocyte globulin 5 (1) 76 (5) 561 (34) 116 (50) 39 (13)
 Alemtuzumab 0 33 (2) 62 (4) 6 (3) 0
 None 388 (99) 1505 (93) 1010 (61) 105 (46) 265 (87)
 Missing 0 13 (<1) 13 (<1) 3 (1) 1 (<1)

BCR-ABL, breakpoint cluster region-Abelson murine leukemia; CMV, cytomegalovirus; CNI, calcineurin inhibitor; MAC, myeloablative conditioning; MMF, mycophenolate mofetil; MTX, methotrexate; NA, not applicable; NMA, non-myeloablative.

*

Other/not specified: Native American (n = 30), Pacific Islander (n = 20), non-resident of the United States (n = 291), not specified (n = 156), Hispanic, excluding White Hispanic (n = 213).

CIBMTR cytogenetics criteria definition: Poor: Ph+/t(9:22)/BCR-ABL1, t(4:11), 11q23/MLL/KMT2A, hypodiploid (<45), t(8:14), complex (≥3 abnormalities), iAMP21; normal: without any abnormality; other: abnormality count of 1 or 2 abnormalities.