Table 2.

Clinical features of the study cohort

CharacteristicsControl (n = 132)PcGVHD(n = 166)Unclassified (n = 52)P
Age at HCT* 39.8 ± 16.8 40.7 ± 15.5 35.3 ± 18.7 .114 
Weight, kg* 72.0 ± 20.5 68.5 ± 16.7 67.1 ± 20.4 .170 
KPS* 83.0 ± 9.7 74.6 ± 12.0 77.6 ± 12.0 <.001 
TLC, %predicted* 95.3 ± 13.4 74.2 ± 17.9 76.4 ± 15.4 <.001 
RV, %predicted* 88.1 ± 32.5 90.6 ± 42.0 89.8 ± 37.7 .845 
FEV1/FVC, %, pre-bronchodilator* 79.4 ± 7.9 64.9 ± 18.1 76.3 ± 13.1 <.001 
FVC, %predicted, pre-bronchodilator* 96.6 ± 12.4 62.7 ± 17.2 67.5 ± 15.0 <.001 
FEV1, %predicted, pre-bronchodilator* 97.4 ± 12.8 50.3 ± 16.3 64.0 ± 14.2 <.001 
FEF 25-75%, %predicted* 94.0 ± 27.9 39.9 ± 31.9 57.8 ± 26.5 <.001 
DLCO adj, %predicted* 74.8 ± 18.4 53.7 ± 16.7 57.9 ± 16.7 <.001 
Different types of cGVHD treatment*, 3.8 ± 1.9 5.1 ± 2.2 5.2 ± 2.2 <.001 
Time from HCT to cGVHD diagnosis (days)* 395.1 ± 741.0 319.7 ± 345.8 282.0 ± 208.7 .308 
Time from HCT to adjudicative PFT (days)* 1822.8 ± 1640.6 2113.6 ± 1579.2 1869.6 ± 1345.4 .253 
Recipient sex Female 62 (46.9) 74 (44.6) 20 (38.4) .579 
Recipient race White 112 (86.2) 148 (89.2) 47 (90.4) .635 
HCT location Local 113 (85.6) 154 (92.8) 45 (86.5) .115 
 NIH 19 (14.4) 12 (7.2) 7 (13.5)  
Pre-HCT tobacco use 34 (25.9) 51 (30.7) 12 (23.1) .471 
HCT indication AML, MDS, ALL 61 (46.2) 96 (57.8) 26 (50.0) .037 
 CML, MPN 16 (12.1) 19 (11.5) 3 (5.8)  
 CLL, HL, NHL, MM 48 (36.4) 43 (25.9) 15 (28.9)  
 Others 7 (5.3) 8 (4.8) 8 (15.4)  
Disease status at HCT CR 47 (39.8) 92 (60.1) 21 (44.7) .003 
HLA MRD 69 (52.7) 90 (54.2) 18 (36.7) .037 
 MUD 40 (30.5) 53 (31.9) 28 (57.1)  
 MMUD 16 (12.2) 16 (9.6) 2 (4.1)  
 Haploidentical 6 (4.6) 7 (4.2) 1 (2.0)  
Stem cell source PB 98 (77.2) 138 (84.2) 38 (73.1) .233 
 BM 29 (22.8) 26 (15.9) 12 (23.1)  
Conditioning RIC 71 (53.8) 69 (42.1) 25 (50.0) .126 
 MAC 61 (46.2) 95 (57.9) 25 (50.0)  
Busulfan 44 (34.4) 76 (48.1) 16 (32.0) .026 
TBI 54 (41.2) 64 (39.0) 20 (39.2) .924 
GVHD prophylaxis CNI + MTX 62 (50.8) 70 (46.1) 29 (59.2) .269 
Second malignancy 20 (15.1) 34 (20.5) 10 (19.2) .488 
Acute GVHD 92 (69.7) 120 (72.3) 38 (73.1) .851 
cGVHD global Mild 6 (4.5) 1 (0.6) <.001 
severity Moderate 50 (37.9) 15 (9.0) 13 (25.0)  
 Severe 76 (57.6) 150 (90.4) 39 (75.0)  
Relapse/refractory primary malignancy 22 (16.7) 22 (13.3) 8 (15.4) .708 
CharacteristicsControl (n = 132)PcGVHD(n = 166)Unclassified (n = 52)P
Age at HCT* 39.8 ± 16.8 40.7 ± 15.5 35.3 ± 18.7 .114 
Weight, kg* 72.0 ± 20.5 68.5 ± 16.7 67.1 ± 20.4 .170 
KPS* 83.0 ± 9.7 74.6 ± 12.0 77.6 ± 12.0 <.001 
TLC, %predicted* 95.3 ± 13.4 74.2 ± 17.9 76.4 ± 15.4 <.001 
RV, %predicted* 88.1 ± 32.5 90.6 ± 42.0 89.8 ± 37.7 .845 
FEV1/FVC, %, pre-bronchodilator* 79.4 ± 7.9 64.9 ± 18.1 76.3 ± 13.1 <.001 
FVC, %predicted, pre-bronchodilator* 96.6 ± 12.4 62.7 ± 17.2 67.5 ± 15.0 <.001 
FEV1, %predicted, pre-bronchodilator* 97.4 ± 12.8 50.3 ± 16.3 64.0 ± 14.2 <.001 
FEF 25-75%, %predicted* 94.0 ± 27.9 39.9 ± 31.9 57.8 ± 26.5 <.001 
DLCO adj, %predicted* 74.8 ± 18.4 53.7 ± 16.7 57.9 ± 16.7 <.001 
Different types of cGVHD treatment*, 3.8 ± 1.9 5.1 ± 2.2 5.2 ± 2.2 <.001 
Time from HCT to cGVHD diagnosis (days)* 395.1 ± 741.0 319.7 ± 345.8 282.0 ± 208.7 .308 
Time from HCT to adjudicative PFT (days)* 1822.8 ± 1640.6 2113.6 ± 1579.2 1869.6 ± 1345.4 .253 
Recipient sex Female 62 (46.9) 74 (44.6) 20 (38.4) .579 
Recipient race White 112 (86.2) 148 (89.2) 47 (90.4) .635 
HCT location Local 113 (85.6) 154 (92.8) 45 (86.5) .115 
 NIH 19 (14.4) 12 (7.2) 7 (13.5)  
Pre-HCT tobacco use 34 (25.9) 51 (30.7) 12 (23.1) .471 
HCT indication AML, MDS, ALL 61 (46.2) 96 (57.8) 26 (50.0) .037 
 CML, MPN 16 (12.1) 19 (11.5) 3 (5.8)  
 CLL, HL, NHL, MM 48 (36.4) 43 (25.9) 15 (28.9)  
 Others 7 (5.3) 8 (4.8) 8 (15.4)  
Disease status at HCT CR 47 (39.8) 92 (60.1) 21 (44.7) .003 
HLA MRD 69 (52.7) 90 (54.2) 18 (36.7) .037 
 MUD 40 (30.5) 53 (31.9) 28 (57.1)  
 MMUD 16 (12.2) 16 (9.6) 2 (4.1)  
 Haploidentical 6 (4.6) 7 (4.2) 1 (2.0)  
Stem cell source PB 98 (77.2) 138 (84.2) 38 (73.1) .233 
 BM 29 (22.8) 26 (15.9) 12 (23.1)  
Conditioning RIC 71 (53.8) 69 (42.1) 25 (50.0) .126 
 MAC 61 (46.2) 95 (57.9) 25 (50.0)  
Busulfan 44 (34.4) 76 (48.1) 16 (32.0) .026 
TBI 54 (41.2) 64 (39.0) 20 (39.2) .924 
GVHD prophylaxis CNI + MTX 62 (50.8) 70 (46.1) 29 (59.2) .269 
Second malignancy 20 (15.1) 34 (20.5) 10 (19.2) .488 
Acute GVHD 92 (69.7) 120 (72.3) 38 (73.1) .851 
cGVHD global Mild 6 (4.5) 1 (0.6) <.001 
severity Moderate 50 (37.9) 15 (9.0) 13 (25.0)  
 Severe 76 (57.6) 150 (90.4) 39 (75.0)  
Relapse/refractory primary malignancy 22 (16.7) 22 (13.3) 8 (15.4) .708 

ALL, acute lymphoblastic leukemia; AML, acute myeloid leukemia; BM, bone marrow; CLL, chronic lymphocytic leukemia; CML, chronic myelogenous leukemia; CR, complete remission; HL, Hodgkin’s lymphoma; MAC, myeloablative conditioning; MDS, myelodysplastic syndrome; MM, multiple myeloma; MMUD, mismatched unrelated donor; MPN, myeloproliferative neoplasm; MRD, matched related donor; MUD, matched unrelated donor; NHL, non-Hodgkin’s lymphoma; PB, peripheral blood; RIC, reduced intensity conditioning; RV, residual volume; TBI, total body irradiation.

*

Mean ± SD, analysis of variance test.

Excluding topical treatment such as topical corticosteroids.

Count (percentage), χ2 test.

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