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. Author manuscript; available in PMC: 2018 Aug 1.
Published in final edited form as: Biol Blood Marrow Transplant. 2017 Apr 25;23(8):1250–1256. doi: 10.1016/j.bbmt.2017.04.019

Table 1.

Patient characteristics

Characteristic, no. (%) Discovery cohort (n=40) Verification cohort (n=127)
IPA 1: Prior acute GVHD− IPA 2: Prior acute GVHD + Subsequent chronic GVHD
Subsequent chronic GVHD Subsequent chronic GVHD
Yes (n=10) No (n=10) Yes (n=10) No (n=10) Yes (n=82) No (n=45)
Prior acute GVHD 0 (0) 0 (0) 10 (100) 10 (100) 41 (50) 24 (53)
Median patient age at transplantation (range) 54 (36–63) 43 (32–59) 48 (28–71) 48 (19–64) 55 (26–73) 52 (20–69)
Median months from sample collection to chronic GVHD 2.7 (1.4–5.0) NA 5.2 (0.5–16) NA 4.9 (0.5–31) NA
Patient gender
 Male 5 (50) 5 (50) 5 (50) 5 (50) 58 (71) 25 (56)
 Female 5 (50) 5 (50) 5 (50) 5 (50) 24 (29) 20 (44)
Disease risk at transplantation*
 Standard 5 (50) 5 (50) 3 (30) 5 (50) 27 (33) 17 (38)
 High 5 (50) 5 (50) 7 (70) 5 (50) 55 (67) 28 (62)
HLA and donor type
 Matched related 7 (70) 5 (50) 6 (60) 5 (50) 33 (40) 19 (42)
 Matched unrelated 2 (20) 3 (30) 4 (40) 3 (30) 36 (44) 17 (38)
 HLA mismatched 1 (10) 2 (20) 0 (0) 2 (20) 13 (16) 9 (20)
Conditioning regimen
 High intensity 4 (40) 7 (70) 5 (50) 8 (80) 45 (55) 21 (47)
 Reduced intensity 6 (60) 3 (30) 5 (50) 2 (20) 37 (45) 24 (53)
Graft source
 Bone marrow 0 (0) 2 (20) 0 (0) 4 (40) 6 (7) 11 (24)
 Mobilized blood cells 10 (100) 8 (80) 10 (100) 6 (60) 76 (93) 32 (71)
 Umbilical cord blood 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 2 (4)
T cell depletion
 Antithymocyte globulin 0 (0) 1 (10) 0 (0) 2 (20) 1 (1) 1 (2)
 Campath 0 (0) 0 (0) 0 (0) 0 (0) 0 (0) 0 (0)
Immunosuppressive drugs at sample collection
 Calcineurin inhibitor 10 (100) 10 (100) 8 (80) 10 (100) 80 (98) 41 (91)
 Mycophenolate mofetil 1 (10) 0 (0) 2 (20) 0 (0) 21 (26) 12 (27)
 Sirolimus 0 (0) 0 (0) 0 (0) 0 (0) 3 (4) 1 (2)

IPA indicates intact protein analysis; GVHD, graft-versus-host disease; and HLA, human leukocyte antigen.

*

The standard-risk category included chronic myeloid leukemia in chronic phase, acute leukemia in first remission, myelodysplastic syndrome without excess blasts, and non-malignant diseases. The high-risk category included all other diseases and stages.