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Published online before print April 12, 2006
Eur Respir J 2006, doi:10.1183/09031936.06.00032605
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ORIGINAL ARTICLE

Long term clinical effects of IFN-{gamma}-1b and colchicine in idiopathic pulmonary fibrosis

K.M. Antoniou 1, A.G. Nicholson 2, M. Dimadi 3, K. Malagari 4, P. Latsi 5, A. Rapti 3, N. Tzanakis 1, R. Trigidou 6, V. Polychronopoulos 7, D. Bouros 8*

1 Dept of Pneumonology, Medical School University of Crete, Heraklion, Greece
2 Dept of Histopathology, Royal Brompton Hospital, London, England
3 Dept of Pneumonology of "Sotiria Chest Hospital" Athens, Greece
4 Dept of Radiology Medical School University of Athens, Athens, Greece
5 Dept of Pneumonology, Medical School University of Athens, Athens, Greece
6 Dept of Histopathology, "Sotiria Chest Hospital" Athens, Greece
7 Dept of Pneumonology "Sismanoglion Hospital", Athens Greece
8 Dept of Pneumonology, Democritus Medical School University of Thrace, Alexandroupolis, Greece

* To whom correspondence should be addressed. E-mail: bouros{at}med.duth.gr.


   Abstract

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-{gamma}-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-{gamma}-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-{gamma}-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-{gamma}-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-{gamma}-1b may improve survival and outcome in patients with mild to moderate IPF. Further studies are needed to verify these results.

Keywords:  Colchicine, idiopathic pulmonary fibrosis, interferon gamma-1b, outcome, survival, treatment




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