期刊
CHEST
卷 124, 期 1, 页码 177-185出版社
ELSEVIER
DOI: 10.1378/chest.124.1.177
关键词
BAL; etanercept; sarcoidosis; tumor necrosis factor-alpha
Background: Tumor necrosis factor (TNF)-alpha is produced by macrophages and other cells, and is believed to participate in granulomatous inflammation. Targeted antagonism of TNF-alpha has been proposed as a novel treatment strategy for sarcoidosis. Etanercept is a dimeric fusion protein that binds specifically to TNF-alpha, rendering it biologically inactive. Objective: To assess whether etanercept has potential efficacy in the treatment of progressive pulmonary sarcoidosis. Design: Prospective, open-label, phase-2 treatment trial. Setting: Mayo Clinic, Rochester, MN. Patients: Stage 11 or III progressive pulmonary sarcoidosis. Intervention: Etanercept, 25 mg subcutaneously twice weekly. Measurements: Pulmonary function, chest radiographs, dyspnea, and TNF-alpha levels in serum and BAIL fluid. Results: The study was terminated after the enrollment of 17 patients due to an early-stop clause of the pretrial study design related to excessive treatment failures. Neither absolute levels of TNF-alpha nor TNF-alpha activity in the serum, BAL fluid, or alveolar macrophages were able to predict which patients would respond to etanercept. Conclusions: In patients with progressive stage 11 or III pulmonary sarcoidosis, etanercept was frequently associated with early or late treatment failure. These data would not support the design of a large multicenter randomized trial comparing etanercept with conventional corticosteroid therapy.
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