Table 1.

Population characteristics

MSKCC cohortSheba cohort
Recipient age, median (IQR), y 56 (46-64) 61 (53-65) 
Age <60 y 358 (62) 110 (48) 
Age ≥60 y 215 (38) 120 (52) 
Recipient sex   
 Male 329 (57) 144 (63) 
 Female 244 (43) 86 (37) 
Karnofsky performance status   
 90-100 365 (64) 189 (82) 
 <90 207 (36) 28 (12) 
 Missing 1 (0.2) 13 (6) 
HCT-CI   
 0 132 (23) 37 (16) 
 1 98 (17) 47 (20) 
 2 106 (18) 38 (17) 
 3 116 (20) 40 (17) 
 ≥4 121 (21) 68 (30) 
Recipient CMV serostatus   
 Absent 222 (39) 42 (19) 
 Present 351 (61) 182 (81) 
Diagnosis   
 Acute myeloid leukemia 217 (38) 53 (23) 
 Myelodysplastic syndrome 125 (22) 57 (25) 
 Multiple myeloma 115 (20) 17 (7) 
 Acute lymphoblastic leukemia 57 (10) 15 (7) 
 Myeloproliferative neoplasm 31 (5) 4 (2) 
 Chronic myeloid leukemia 17 (3) 3 (1) 
 Other leukemia 9 (2) 0 (0) 
 Lymphoma 0 (0) 81 (35) 
Disease risk*   
 Low/intermediate 387 (68) 138 (60) 
 High 140 (24) 92 (40) 
 Unclassifiable 46 (8) 0 (0) 
Time from Dx to HCT, median (IQR), mo 7 (5-25) 12 (4-34) 
Donor/recipient sex   
 Female/male 114 (20) 52 (23) 
 Other 459 (80) 175 (77) 
Donor type   
 Matched related 192 (34) 100 (43) 
 Matched unrelated 283 (49) 98 (43) 
 HLA mismatched 98 (17) 32 (14) 
HCT year, median (IQR) 2014 (2012-2016) 2013 (2012-2014) 
Regimen (%)   
 Melphalan based 436 (76) NA 
 TBI based 137 (24) NA 
 Fludarabine-treosulfan (30 g/m2NA 33 (14) 
 Fludarabine-treosulfan (36-42 g/m2NA 156 (68) 
 Fludarabine-melphalan (100 mg/m2NA 27 (12) 
 Fludarabine-melphalan (140 mg/m2NA 14 (6) 
MSKCC cohortSheba cohort
Recipient age, median (IQR), y 56 (46-64) 61 (53-65) 
Age <60 y 358 (62) 110 (48) 
Age ≥60 y 215 (38) 120 (52) 
Recipient sex   
 Male 329 (57) 144 (63) 
 Female 244 (43) 86 (37) 
Karnofsky performance status   
 90-100 365 (64) 189 (82) 
 <90 207 (36) 28 (12) 
 Missing 1 (0.2) 13 (6) 
HCT-CI   
 0 132 (23) 37 (16) 
 1 98 (17) 47 (20) 
 2 106 (18) 38 (17) 
 3 116 (20) 40 (17) 
 ≥4 121 (21) 68 (30) 
Recipient CMV serostatus   
 Absent 222 (39) 42 (19) 
 Present 351 (61) 182 (81) 
Diagnosis   
 Acute myeloid leukemia 217 (38) 53 (23) 
 Myelodysplastic syndrome 125 (22) 57 (25) 
 Multiple myeloma 115 (20) 17 (7) 
 Acute lymphoblastic leukemia 57 (10) 15 (7) 
 Myeloproliferative neoplasm 31 (5) 4 (2) 
 Chronic myeloid leukemia 17 (3) 3 (1) 
 Other leukemia 9 (2) 0 (0) 
 Lymphoma 0 (0) 81 (35) 
Disease risk*   
 Low/intermediate 387 (68) 138 (60) 
 High 140 (24) 92 (40) 
 Unclassifiable 46 (8) 0 (0) 
Time from Dx to HCT, median (IQR), mo 7 (5-25) 12 (4-34) 
Donor/recipient sex   
 Female/male 114 (20) 52 (23) 
 Other 459 (80) 175 (77) 
Donor type   
 Matched related 192 (34) 100 (43) 
 Matched unrelated 283 (49) 98 (43) 
 HLA mismatched 98 (17) 32 (14) 
HCT year, median (IQR) 2014 (2012-2016) 2013 (2012-2014) 
Regimen (%)   
 Melphalan based 436 (76) NA 
 TBI based 137 (24) NA 
 Fludarabine-treosulfan (30 g/m2NA 33 (14) 
 Fludarabine-treosulfan (36-42 g/m2NA 156 (68) 
 Fludarabine-melphalan (100 mg/m2NA 27 (12) 
 Fludarabine-melphalan (140 mg/m2NA 14 (6) 

Unless otherwise noted, data are n (%).

CMV, cytomegalovirus; Dx, diagnosis; HCT, hematopoietic cell transplantation; NA, not applicable (regimens specific to individual centers).

*

Disease risk was classified using Center for International Bone and Marrow Transplant Research criteria (MSKCC cohort) and European Society for Blood and Bone Transplantation criteria (Sheba cohort).

Matched donor was defined at an 8/8 HLA allele level for the MSKCC cohort and a 10/10 HLA level at the Sheba Medical Center. Corresponding definitions for mismatched donors were 7/8 and 9/10.

Among patients in the Sheba cohort, 173 (77%) and 51 (23%) received methotrexate-based or mycophenolate mofetil–based GvHD prophylaxis, respectively, and 143 (62%) received anti-thymocyte globulin.

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