Table 1.

Patient characteristics

Discovery cohort (n = 55)Validation cohort 1 (n = 55)Validation cohort 2 (n = 50)
Age at transplantation, y    
 Mean (range) 48 (18-65) 47 (18-66) 46 (18-68) 
Recipient/donor sex    
 Male/female 13 (23.6) 14 (25.5) 11 (22.0) 
 Other combinations 42 (76.4) 41 (74.5) 39 (78.0) 
Underlying disease    
 Acute leukemia 30 (54.5) 40 (72.7) 31 (62.0) 
 Malignant lymphoma 5 (9.1) 5 (9.1) 6 (12.0) 
 MDS/MPN 16 (29.1) 5 (9.1) 7 (14.0) 
 Aplastic anemia 3 (5.5) 5 (9.1) 1 (2.0) 
 Chronic myeloid leukemia 1 (1.8) 0 (0) 3 (6.0) 
 Other 0 (0) 0 (0) 2 (4.0) 
Disease risk*    
 Low risk 51 (92.7) 46 (83.6) 46 (92.0) 
 High risk 4 (7.3) 9 (16.4) 4 (8.0) 
Performance status    
 0-1 54 (98.2) 54 (98.2) 48 (96.0) 
 2-4 1 (1.8) 1 (1.8) 2 (4.0) 
HCT-CI    
 0-1 48 (87.3) 47 (85.5) 42 (84.0) 
 ≥2 7 (12.7) 8 (14.5) 8 (16.0) 
Stem cell source    
 Bone marrow 34 (61.8) 31 (56.4) 25 (50.0) 
 Peripheral blood stem cells 16 (29.1) 19 (34.5) 24 (48.0) 
 Umbilical cord blood 5 (9.1) 5 (9.1) 1 (2.0) 
HLA    
 Match 31 (56.4) 25 (45.5) 30 (60.0) 
 Mismatch 24 (43.6) 30 (54.5) 20 (40.0) 
Type of donor    
 Related 16 (29.1) 19 (34.5) 21 (42.0) 
 Unrelated 39 (70.9) 36 (65.5) 29 (58.0) 
Conditioning regimen    
 Myeloablative 39 (70.9) 39 (70.9) 34 (68.0) 
 Reduced intensity 16 (29.1) 16 (29.1) 16 (32.0) 
GVHD prophylaxis    
 CSA + MTX 47 (85.5) 50 (90.9) 44 (88.0) 
 TAC + MTX 8 (14.5) 5 (9.1) 6(12.0) 
Use of ATG/alemtuzumab    
 No 49 (89.1) 44 (80.0) 37 (74.0) 
 Yes 6 (10.9) 11 (20.0) 13 (26.0) 
Prior acute GVHD§    
 No 16 (29.1) 16 (29.1) 9 (18.0) 
 Yes 39 (70.9) 39 (70.9) 41 (82.0) 
Prior cGVHD§    
 No 29 (52.7) 33 (60.0) 23 (46.0) 
 Yes 26 (47.3) 22 (40.0) 27 (54.0) 
Median days from HSCT to sample acquisition (range) 179 (133-266) 178 (168-274) 181 (168-267) 
Discovery cohort (n = 55)Validation cohort 1 (n = 55)Validation cohort 2 (n = 50)
Age at transplantation, y    
 Mean (range) 48 (18-65) 47 (18-66) 46 (18-68) 
Recipient/donor sex    
 Male/female 13 (23.6) 14 (25.5) 11 (22.0) 
 Other combinations 42 (76.4) 41 (74.5) 39 (78.0) 
Underlying disease    
 Acute leukemia 30 (54.5) 40 (72.7) 31 (62.0) 
 Malignant lymphoma 5 (9.1) 5 (9.1) 6 (12.0) 
 MDS/MPN 16 (29.1) 5 (9.1) 7 (14.0) 
 Aplastic anemia 3 (5.5) 5 (9.1) 1 (2.0) 
 Chronic myeloid leukemia 1 (1.8) 0 (0) 3 (6.0) 
 Other 0 (0) 0 (0) 2 (4.0) 
Disease risk*    
 Low risk 51 (92.7) 46 (83.6) 46 (92.0) 
 High risk 4 (7.3) 9 (16.4) 4 (8.0) 
Performance status    
 0-1 54 (98.2) 54 (98.2) 48 (96.0) 
 2-4 1 (1.8) 1 (1.8) 2 (4.0) 
HCT-CI    
 0-1 48 (87.3) 47 (85.5) 42 (84.0) 
 ≥2 7 (12.7) 8 (14.5) 8 (16.0) 
Stem cell source    
 Bone marrow 34 (61.8) 31 (56.4) 25 (50.0) 
 Peripheral blood stem cells 16 (29.1) 19 (34.5) 24 (48.0) 
 Umbilical cord blood 5 (9.1) 5 (9.1) 1 (2.0) 
HLA    
 Match 31 (56.4) 25 (45.5) 30 (60.0) 
 Mismatch 24 (43.6) 30 (54.5) 20 (40.0) 
Type of donor    
 Related 16 (29.1) 19 (34.5) 21 (42.0) 
 Unrelated 39 (70.9) 36 (65.5) 29 (58.0) 
Conditioning regimen    
 Myeloablative 39 (70.9) 39 (70.9) 34 (68.0) 
 Reduced intensity 16 (29.1) 16 (29.1) 16 (32.0) 
GVHD prophylaxis    
 CSA + MTX 47 (85.5) 50 (90.9) 44 (88.0) 
 TAC + MTX 8 (14.5) 5 (9.1) 6(12.0) 
Use of ATG/alemtuzumab    
 No 49 (89.1) 44 (80.0) 37 (74.0) 
 Yes 6 (10.9) 11 (20.0) 13 (26.0) 
Prior acute GVHD§    
 No 16 (29.1) 16 (29.1) 9 (18.0) 
 Yes 39 (70.9) 39 (70.9) 41 (82.0) 
Prior cGVHD§    
 No 29 (52.7) 33 (60.0) 23 (46.0) 
 Yes 26 (47.3) 22 (40.0) 27 (54.0) 
Median days from HSCT to sample acquisition (range) 179 (133-266) 178 (168-274) 181 (168-267) 

Unless otherwise indicated, data are n (%).

ATG, anti-thymocyte globulin; CSA, cyclosporine; HCT-CI, hematopoietic cell transplantation-specific comorbidity index; MDS, myelodysplastic syndrome; MPN, myeloproliferative neoplasm; MTX, methotrexate; TAC, tacrolimus.

*

Disease risk was categorized as low risk and high risk. High risk was defined as any hematological malignancy in noncomplete remission. Other conditions were considered low risk.

Performance status was evaluated by the Eastern Cooperative Oncology Group scale.

Conditioning intensity was classified based on criteria from the Center for International Blood and Marrow Transplant Research.

§

History of GVHD at sample acquisition.

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