Azathioprine and Prednisone in the Treatment of Idiopathic Pulmonary Fibrosis

Overview

Idiopathic pulmonary fibrosis (IPF) is a diffuse lung disease, associated with the histological appearance of usual interstitial pneumonia (UIP), with an inexorably deteriorating clinical course. Prognosis is poor, reported median survival is less than 3 years. The prevalence is estimated as being 3 to 10 per 100.000 in different Western populations. To date, no pharmacological therapy has been proven to alter or reverse the pathogenic process of IPF. Most treatments trials have been observational case series of small patient populations and very few have been randomized, prospective and placebo-controlled. Two recent Cochrane reviews investigated the role of corticosteroids and other immunomodulatory agents and concluded that there is no evidence for their use in IPF. Most current therapies are targeted to suppress the inflammatory component of the disease, based on the theory that it would be chronic alveolar inflammation which leads to parenchymal remodeling and fibrosis. Recently, a hypothesis that has gained acceptance suggests that fibrosis may result directly from alveolar injury, promoting an abnormal fibrogenic repair mediated by fibroblasts and myofibroblasts. One of the cytotoxic agents most widely used and better tolerated in the management of IPF is azathioprine. Based upon limited data available and from a single small high quality randomized controlled trial (RCT), this drug appears to confer, given in conjunction with prednisone, a marginal long term survival advantage. Since this combination therapy is associated serious adverse effect, we planned to design a trial of low dose corticosteroid and azathioprine versus placebo in management of IPF, evaluating progression-free survival. Our study hypothesis is: Combined therapy with azathioprine and corticosteroids improves progression-free survival in patients with the diagnosis of IPF.

We will evaluate all adult patients consecutively referred from March 2005 to the Instituto Nacional del Tórax (Thorax National Institute), Santiago, Chile for diagnostic evaluation of Pulmonary Fibrosis. The routine evaluation will include, when indicated, the following steps: * History: * Age * Genre * Duration of symptoms before first consultation * Smoking status * Search for collagen vascular disease * Family history of pulmonary fibrosis * Occupational exposures * Drug ot toxic exposures * Physical examination: search of crackles and finger clubbing. * Laboratory data: * Complete blood bell count * BUN * Creatinine * Liver enzymes * Antinuclear antigens * Erythrocyte sedimentation rate * Rheumatoid factor * HIV * Antineutrophil cytoplasmic antibody (in appropiate clinical setting) * Antiglomerular basement antibody (in appropiate clinical setting) * Modified Medical Research Council Dyspnea Scale (MMRC) (10) * Chronic Respiratory Questionnaire (CRQ) (11) * Pulmonary function tests: * Spirometry * Plethismographic lung volumes * DLco * Composite physiologic index (12) * Exercise testing: * Six-Minute Walk Test (6MWT) * Resting and 6 minute SpO2 * Presence or absence of desaturation to 88% or lower at the end of the six minute walk (13) * Walked distance * Pre and post modified Borg dyspnea scores * Timed walk test (14) * Arterial blood gas analysis in rest and exercise, calculating the difference between alveolar and arterial oxygen tension (P(A-a)O2) at rest and after exercise. * Radiologic studies: * Chest radiography * HRCT: * Definite or probable idiopathic pulmonary fibrosis (15): * Definitive criteria: presence of lung volume reduction, reticular abnormalities, traction bronchiectasis, or both, with a basal and peripheral predominance; the presence of honeycombing with a basal and peripheral predominance; and the absence of atypical features of usual interstitial pneumonia - micronodules, peribronchovascular nodules, consolidation, isolated (nonhoneycombing) cysts, ground-glass attenuation (or if present, less extensive than the reticular opacity), and mediastinal adenopathies (or if present, too limited to be visible on a chest radiography). * Probable criteria: presence of a bilateral, predominantly basal and subpleural reticular pattern with subpleural cysts (honeycombing), traction bronchiectasis, or both in the absence of atypical features of UIP. * Scoring of the extent of lung fibrosis (16). * Bronchoscopy: * Bronchoalveolar lavage: cellular analysis and CD4/CD8 ratio. * Transbronchial biopsy. * Surgical lung biopsy: * Number * Site/Side * Type of surgery: open vs thoracoscopic * Histologic features (3) Those patients with IPF diagnosed on the basis of clinical and radiographic criteria alone according to the ATS/ERS consensus committee (3), and/or with a biopsy proven histological pattern of UIP, will be selected to the randomization process, after they have signed the written informed consent.