Eur Respir J 2006, doi:10.1183/09031936.06.00032605
Long term clinical effects of IFN-
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| Abstract |
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Idiopathic Pulmonary Fibrosis (IPF/UIP) is a deadly disease with no effective treatment. The purpose of this randomized, prospective, multicenter study was to characterize the clinical effects of IFN-
-1b administered subcutaneously thrice weekly versus colchicine for two years. This study had not prespecified endpoints.
Fifty consecutive IPF patients were randomized. Patients with mild-moderate IPF were eligible for the study if they had histologically proven IPF or, in the absence of surgical biopsy, fulfilment of the ERS/ATS criteria.
In the intent-to-treat population, 5 of 32 (15.6%) IFN-
-1b patients and 7 of 18 (38,8%) colchicine patients died (p=0.028) after a median period of follow-up of 25 months Patients treated with IFN-
-1b had a better outcome after two years of therapy (p=0.01), and less symptoms as assessed by the St George Questionnaire after 12 months of therapy (p=0.01). Also, IFN-
-1b group had a higher FVC% predicted (p=0.04) after 24 months of treatment. No significant differences were detected at rest PO2, TLC % predicted, TLCO % predicted, and HRCT scoring between the two treatment groups.
Our data suggest that long term treatment with IFN-
-1b may improve survival and outcome in patients with mild to moderate IPF. Further studies are needed to verify these results.
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