Etanercept for the treatment of stage II and III progressive pulmonary sarcoidosis.

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 II 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 BAL 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 II 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.