TABLE 1.
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.