TABLE 1

Baseline characteristics and lung function at initiation of nintedanib

Patients126
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
 Male59 (47)
 Female67 (53)
ILD diagnosis
 fHP44 (34.9)
 CTD-ILD44 (34.9)
 Unclassifiable IIP9 (7.1)
 Fibrotic NSIP8 (6.3)
 Fibrotic OP4 (3.2)
 PPFE3 (2.4)
 Asbestosis3 (2.4)
 Smoking-related ILD3 (2.4)
 Familial PF1 (0.8)
 Fibrotic sarcoid1 (0.8)
 DIP1 (0.8)
 HIV-associated ILD1 (0.8)
 Other4 (3.2)
Smoking status
 Current smoker2 (1.6)
 Ex-smoker46 (36.5)
 Never-smoker63 (50)
 No data15 (11.9)
Hospital
 Guy's and St Thomas' NHS Foundation trust10 (7.9)
 Manchester University NHS Foundation Trust13 (10.3)
 North Bristol NHS Trust3 (2.4)
 Oxford University Hospital16 (12.7)
 Royal Papworth Hospital15 (11.9)
 Royal Brompton Hospital61 (48.4)
 Royal Devon and Exeter Hospital4 (3.2)
 University Hospital Birmingham4 (3.2)
MRC dyspnoea score
 14 (3)
 218 (14)
 326 (21)
 427 (21)
 516 (13)
 No data35 (28)
Home oxygen (ambulatory/LTOT)
 Yes79 (62.7)
 No45 (35.7)
 Unknown2 (1.6)
Fibrotic pattern on CT
 UIP30 (24)
 Non-UIP95 (75)
 No data1 (0.8)
Indication for starting nintedanib
 Progressive symptoms111 (88)
 Lung function decline100 (79)
 CT progression85 (67)
Concurrent immunosuppression
 Yes113 (90)
 No13 (10)
 Prednisolone86 (68)
 Mycophenolate mofetil70 (56)
 Azathioprine6 (5)
 Hydroxychloroquine13 (10)
 Leflunomide3 (2)
 Rituximab9 (7)
 Tacrolimus1 (0.8)
 Methotrexate3 (2)
Change in immunosuppression following nintedanib initiation
 Unchanged76 (60)
 Increased29 (23)
 Decreased13 (10)
 Other8 (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.