Table 1.

HCT cohort demographics and clinical characteristics

CharacteristicN = 37 pairs (%) or median (IQR)
Recipient age, y 47 (39.5, 54) 
Recipient sex  
 Female 14 (38) 
Race/ethnicity (donor-recipient)  
 White 28 (76) 
 Asian/Pacific Islander 5 (14) 
 Hispanic (mixed race) 3 (8) 
 Black 1 (3) 
Donor age 48.5 (36, 55) 
Donor type  
 Related 36 (97) 
 Unrelated 1 (3) 
Donor sex  
 Female 22 (59) 
 HLA-matched 36 (97) 
 HLA-mismatched (6/10 match) 1 (3) 
Underlying disease  
 AML 12 (32) 
 ALL 2 (5) 
 CML 12 (32) 
 CLL 2 (5) 
 Myelodysplastic syndromes 6 (16) 
 Non-Hodgkin lymphoma 3 (8) 
Disease severity  
 Early disease 23 (62) 
 Intermediate disease 7 (19) 
 Advanced disease 7 (19) 
Cell source*  
 Bone marrow 11 (30) 
 Peripheral blood 27 (73) 
Treatment year  
 1999-2003 33 (89) 
 2012-2013 4 (13) 
CMV serostatus of pair  
 D+/R+ 21 (57) 
 D+/R 8 (22) 
 D/R+ 5 (14) 
 D/R 3 (8) 
Previous treatment regimens  
 Anti-CD20 3 (8) 
 Lymphodepletion 13 (35) 
 Intensive chemotherapy (any) 19 (51) 
Conditioning regimen  
 Bu/Cy, + ATG (1) or RAB (1) 26 (70) 
 TBI, + Cy (5) or VP-16 (1) 8 (22) 
 Bu, Flu 3 (8) 
GVHD prophylaxis  
 CSA, MTX 31 (84) 
 CSA, Cy 4 (11) 
 CSA, MMF 2 (5) 
Systemic GVHD (by NIH criteria)  
 Yes 25 (68) 
CharacteristicN = 37 pairs (%) or median (IQR)
Recipient age, y 47 (39.5, 54) 
Recipient sex  
 Female 14 (38) 
Race/ethnicity (donor-recipient)  
 White 28 (76) 
 Asian/Pacific Islander 5 (14) 
 Hispanic (mixed race) 3 (8) 
 Black 1 (3) 
Donor age 48.5 (36, 55) 
Donor type  
 Related 36 (97) 
 Unrelated 1 (3) 
Donor sex  
 Female 22 (59) 
 HLA-matched 36 (97) 
 HLA-mismatched (6/10 match) 1 (3) 
Underlying disease  
 AML 12 (32) 
 ALL 2 (5) 
 CML 12 (32) 
 CLL 2 (5) 
 Myelodysplastic syndromes 6 (16) 
 Non-Hodgkin lymphoma 3 (8) 
Disease severity  
 Early disease 23 (62) 
 Intermediate disease 7 (19) 
 Advanced disease 7 (19) 
Cell source*  
 Bone marrow 11 (30) 
 Peripheral blood 27 (73) 
Treatment year  
 1999-2003 33 (89) 
 2012-2013 4 (13) 
CMV serostatus of pair  
 D+/R+ 21 (57) 
 D+/R 8 (22) 
 D/R+ 5 (14) 
 D/R 3 (8) 
Previous treatment regimens  
 Anti-CD20 3 (8) 
 Lymphodepletion 13 (35) 
 Intensive chemotherapy (any) 19 (51) 
Conditioning regimen  
 Bu/Cy, + ATG (1) or RAB (1) 26 (70) 
 TBI, + Cy (5) or VP-16 (1) 8 (22) 
 Bu, Flu 3 (8) 
GVHD prophylaxis  
 CSA, MTX 31 (84) 
 CSA, Cy 4 (11) 
 CSA, MMF 2 (5) 
Systemic GVHD (by NIH criteria)  
 Yes 25 (68) 

ALL, acute lymphoblastic leukemia; AML, acute myeloid leukemia; ATG, antithymocyte globulin; Bu, busulfan; CLL, chronic lymphocytic leukemia; CML, chronic myeloid leukemia; CSA, cyclosporine; Cy, cyclophosphamide; Flu, fludarabine; MMF, mycophenolate mofetil; MTX, methotrexate; NIH, National Institutes of Health; RAB, radiolabeled antibodies; TBI, total body irradiation; VP-16, etoposide.

*

Totals to 38; 1 person received both types of cells.

Anticancer or lymphodepleting agents given within the 12 mo prior to HCT were considered. The only anti-B-cell therapy given in this cohort was rituximab; no ofatumumab or anti-CD52 was given. Regimens considered to be lymphodepleting included rituximab, fludarabine, high-dose cytarabine, or cycloporin/ifosphamide, or combinations of the preceding.

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