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. Author manuscript; available in PMC: 2015 Feb 2.
Published in final edited form as: Am J Hematol. 2014 Feb 21;89(4):404–409. doi: 10.1002/ajh.23656

TABLE I.

Clinical Characteristics of the BOS and Non-BOS Control Cohorts

BOS, n = 89 cGVHD, n = 89 No cGVHD, n = 87
Age (y) 46.1 (12.1) 44.9 (13) 42 (12.4)a
Male gender 48 (54%) 57 (64%) 49 (56%)
White race 80 (90%) 85 (96%) 85 (98%)
Active smoking at Tx 4 (5%) 5 (6%) 5 (6%)
Pretransplant history of pulmonary diseasec 20 (22%) 10 (11%) 3 (3%)a
Respiratory Illness prior to day 100d 23 (26%) 11 (13%)a 9 (10%)a
CMV positive 40 (45%) 35 (39%) 28 (33%)
Acute GVHDe 40 (45%) 34 (38%) 27 (31%)
Pretransplant PFTs
 Pretransplant FEV1% 89.3 (17) 101 (14.7)a 100.2 (14.8)a
 Pretransplant FVC% 90.9 (16.8) 97.9 (12.6)a 99.4 (14)a
 Pretransplant FEV1/FVC 76.1 (8.8) 79.8 (6.3)a 79.1 (7)a
 Pretransplant TLC% 90.1 (16.8) 94.0 (11.1) 94.9 (12.6)
 Pretransplant RV% 93.0 (30.8) 85.2 (24.6) 87.3 (26.6)
 Pretransplant RV/TLC% 102.7 (24.9) 91.2 (19.4)a 90.8 (26.0)a
 Pretransplant DLCO% 84.4 (22.1) 90.4 (17.8) 88.4 (20.7)
 High-risk diseasef 64 (72%) 61 (69%) 45 (52%)a,b
Cell source
 PBSC 76 (85%) 73 (82%) 55 (63%)a,b
 Bone marrow 10 (11%) 13 (15%) 17 (20%)
 Cord cells 3 (3%) 3 (3%) 14 (16%)a,b
Conditioning regimen
 Busulfan/cyclophosphamidee 4 (5%) 2 (2%) 1 (1%)
 Cyclophosphamide/TBIg 37 (42%) 48 (54%) 55 (63%)a
 Busulfan/fludarabineh 45 (51%) 34(38%) 13(15%)a,b
 Melphalan/fludarabine 3 (3%) 3 (3%) 13 (15%)a,b
 Other 0 (0%) 2 (2%) 5 (6%)a
GVHD prophylaxis
 ATG in conditioning 6 (7%) 5 (6%) 30 (34%)a,b
 Sirolimus post HSCT 51 (57%) 52 (58%) 37 (43%)b
Donor
 Age (y) 35.3 (11.8) 39.4 (12.7)a 33.9 (18.0)
 Female 46 (52%) 32 (36%)a 28 (31%)a
 Gender mismatch 37 (42%) 38 (43%) 42 (48%)
 Unrelated 65 (73%) 50 (66%)a 37 (41%)a,b
 Mismatched 14 (16%) 9 (10%) 15 (17%)
 CMV positive 30 (34%) 28 (32%) 25 (29%)
a

P <0.05 BOS vs cGVHD and no cGVHD controls

b

P <0.05 cGVHD vs no cGVHD controls.

c

Pretransplant history of pulmonary disease included the following diagnoses: asthma, chronic obstructive pulmonary disease, emphysema, chronic bronchitis, and bronchiectasis that were not active at the time of diagnosis.

d

Patients treated for viral or bacterial infection per treating physician prior to day 100.

e

Acute GVHD was graded by consensus grading criteria [38].

f

All diseases other than CML CP1, AML/ALL CR1, MDS RA/RS, or AA are considered high-risk in this analysis.

g

Myeloablative conditioning regimens: cytoxan + total body irradiation 1400 cGY; high dose busulfan cyclophosphamide.

h

Reduced intensity conditioning regimen: fludarabine + low-dose intravenous busulfan (3.2–6.4 mg/kg).