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. 2023 Mar 20;9(2):00423-2022. doi: 10.1183/23120541.00423-2022

TABLE 1.

Baseline characteristics and lung function at initiation of nintedanib

Patients 126
Age (years) 60±13
Baseline lung function
 FVC (L) (n=103) 1.86±0.70
 FVC (% pred) (n=102) 57.62±18.56
DLCO (% pred) (n=79) 32.66±11.04
KCO (% pred) (n=74) 65.85±18.97
Gender
 Male 59 (47)
 Female 67 (53)
ILD diagnosis
 fHP 44 (34.9)
 CTD-ILD 44 (34.9)
 Unclassifiable IIP 9 (7.1)
 Fibrotic NSIP 8 (6.3)
 Fibrotic OP 4 (3.2)
 PPFE 3 (2.4)
 Asbestosis 3 (2.4)
 Smoking-related ILD 3 (2.4)
 Familial PF 1 (0.8)
 Fibrotic sarcoid 1 (0.8)
 DIP 1 (0.8)
 HIV-associated ILD 1 (0.8)
 Other 4 (3.2)
Smoking status
 Current smoker 2 (1.6)
 Ex-smoker 46 (36.5)
 Never-smoker 63 (50)
 No data 15 (11.9)
Hospital
 Guy's and St Thomas' NHS Foundation trust 10 (7.9)
 Manchester University NHS Foundation Trust 13 (10.3)
 North Bristol NHS Trust 3 (2.4)
 Oxford University Hospital 16 (12.7)
 Royal Papworth Hospital 15 (11.9)
 Royal Brompton Hospital 61 (48.4)
 Royal Devon and Exeter Hospital 4 (3.2)
 University Hospital Birmingham 4 (3.2)
MRC dyspnoea score
 1 4 (3)
 2 18 (14)
 3 26 (21)
 4 27 (21)
 5 16 (13)
 No data 35 (28)
Home oxygen (ambulatory/LTOT)
 Yes 79 (62.7)
 No 45 (35.7)
 Unknown 2 (1.6)
Fibrotic pattern on CT
 UIP 30 (24)
 Non-UIP 95 (75)
 No data 1 (0.8)
Indication for starting nintedanib
 Progressive symptoms 111 (88)
 Lung function decline 100 (79)
 CT progression 85 (67)
Concurrent immunosuppression
 Yes 113 (90)
 No 13 (10)
 Prednisolone 86 (68)
 Mycophenolate mofetil 70 (56)
 Azathioprine 6 (5)
 Hydroxychloroquine 13 (10)
 Leflunomide 3 (2)
 Rituximab 9 (7)
 Tacrolimus 1 (0.8)
 Methotrexate 3 (2)
Change in immunosuppression following nintedanib initiation
 Unchanged 76 (60)
 Increased 29 (23)
 Decreased 13 (10)
 Other 8 (6)

Data are presented as n, mean±sd or n (%). FVC: forced vital capacity; DLCO: diffusing capacity of the lung for carbon monoxide; KCO: transfer coefficient of the lung for carbon monoxide; ILD: interstitial lung disease; fHP: fibrotic hypersensitivity pneumonitis; CTD-ILD: connective tissue disease-associated ILD; IIP: idiopathic interstitial pneumonia; NSIP: nonspecific interstitial pneumonia; OP: organising pneumonia; PPFE: pleuroparenchymal fibroelastosis; PF: pulmonary fibrosis; DIP: desquamative interstitial pneumonia; NHS: National Health Service; MRC: Medical Research Council; LTOT: long-term oxygen therapy; CT: computed tomography; UIP: usual interstitial pneumonia.