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. Author manuscript; available in PMC: 2017 Nov 1.
Published in final edited form as: J Immunol. 2016 Sep 30;197(9):3490–3503. doi: 10.4049/jimmunol.1601054

Table I.

CGVHD patient demographics

Patient Microarray N = 26 Nanostring N = 69*
Median (Range) Number of Patients Median (Range) Number of Patients
Age 42 (21–63) 46 (21–68)
Sex (Male/Female) 17/9 38/31
HSCT Myeloablative/Nonmyeloablative 16/10 39/30
Donor: Related/ Unrelated/Haplo 14/12/0 43/26/0
Donor Source: BM/PBSC/CB 3/23/0 13/55/1
TBI 13/13 27/42
Months from Transplant to Evaluation 29 (6–74) 38 (5–258)
Months from CGVHD Diagnosis 20 (2–67) 27 (0–240)
Onset: (Progressive/Quiescent/De novo) 7/10/9 26/20/24
Lines of Prior Systemic Therapy 4 (2–8) 4 (0–9)
Current Systemic Therapy
 Prednisone 17 46
 Tacrolimus 15 24
 MMF 8 20
 Sirolimus 4 14
 ECP 4 14
 Imatinib 4 5
 Cyclosporine 1 6
 None 2 9
 Other 1 4
Number of Organs Involved 5 (2–7) 5 (2–8)
CGVHD Organ Involvement (0/1/2/3)
 Vulvo/Vaginal (female only) 1/4/2/2 13/10/4/4
 Oral 9/13/3/1 20/37/9/3
 Eye 2/11/9/3 12/26/26/5
 Liver 12/11/3/0 35/23/10/1
 GI 16/6/3/1 44/18/5/2
 Lung 6/14/3/3 17/28/17/7
 Joints/Fascia 6/5/13/2 18/16/28/7
 Skin 0/2/6/18 9/6/15/39
%Body Surface Area (0, <25%, <50%, >50%)
 Erythematous 2/19/4/1 21/38/8/2
 Dermal Sclerotic 8/14/2/2 25/32/9/3
 Deep Sclerotic 7/7/8/4 27/17/15/10
Severity§ (Mild/Moderate/Severe) 0/7/19 0/19/50
*

All 26 CGVHD patients assessed by microarray, as well as 43 additional CGVHD patients, were analyzed in the Nanostring cohort

Other systemic therapies: hydroxychloroquine, montelukast, methotrexate, rituximab

Some patients had combinations of erythematous, dermal and deep sclerotic areas of their skin and were included in more than one category

§

CGVHD Severity as assessed at time of NIH protocol enrollment