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. Author manuscript; available in PMC: 2026 Oct 1.
Published in final edited form as: Am J Respir Crit Care Med. 2026 Apr 1;212(4):768–777. doi: 10.1093/ajrccm/aamag006

Table 2.

Baseline clinical characteristics and outcomes between endotypes for discovery and validation cohorts.

Characteristic Discovery Validation
Class 1 Class 2 P-value Class 1 Class 2 P-value
N = 475 N = 201 N = 409 N = 176
Age (years) 62 (±13) 65 (±11) 0.033 63 (±12) 65 (±11) 0.045
Diagnosis >0.9 >0.9
 CTD-ILD 220 (46%) 90 (45%) 167 (41%) 73 (41%)
 fHP 138 (29%) 59 (29%) 99 (24%) 41 (23%)
 IIP 117 (25%) 52 (26%) 143 (35%) 62 (35%)
Sex (female) 296 (62%) 119 (59%) 0.4 224 (55%) 96 (55%) >0.9
Race/Ethnicity 0.064 0.11
 White 322 (68%) 152 (76%) 329 (80%) 143 (81%)
 Black 36 (7.6%) 12 (6.0%) 57 (14%) 22 (13%)
 Hispanic 65 (14%) 27 (13%) 1 (0.2%) 4 (2.3%)
 Other/Unknown 52 (11%) 10 (5.0%) 22 (5.4%) 7 (4.0%)
Smoking history 170 (36%) 85 (42%) 0.11 199 (49%) 94 (53%) 0.3
FVC (% predicted) 68 (±19) 60 (±19) <0.001 70 (±20) 60 (±17) <0.001
DLCO (% predicted) 49 (±17) 38 (±16) <0.001 50 (±19) 38 (±14) <0.001
Prior RTX/CYC exposure 31 (6.5%) 13 (6.5%) >0.9 5 (1.2%) 3 (1.7%) 0.7
Prednisone use at blood draw 152 (32%) 108 (54%) <0.001 78 (19%) 41 (23%) 0.2
IS use at blood draw 105 (23%) 51 (26%) 0.4 80 (20%) 46 (26%) 0.076
AF use at blood draw 16 (3.4%) 4 (2.0%) 0.3 18 (4.4%) 8 (4.5%) >0.9
3-year transplant-free survival 372 (78%) 73 (36%) <0.001 340 (83%) 81 (46%) <0.001

Data are shown as mean (±SD) and n (%). Abbreviations: AF, antifibrotic; CTD-ILD, connective tissue disease-associated interstitial lung disease; CYC, cyclophosphamide; DLCO, diffusion capacity of the lung for carbon monoxide; fHP, fibrotic hypersensitivity pneumonitis; FVC, forced vital capacity; IIP, idiopathic interstitial pneumonia; IS, immunosuppressant medication (mycophenolate, azathioprine, rituximab, or cyclophosphamide); RTX, rituximab.