Volume 60, Issue 4 , Pages 565-573, April 2009
A prospective clinical trial of open-label etanercept for the treatment of hidradenitis suppurativa
Background
Medical therapies for hidradenitis suppurativa (HS) are often ineffective. Tumor necrosis factor-α inhibitors may be a potential treatment for patients with moderate to severe HS.
Objectives
We sought to evaluate the safety and efficacy of etanercept for patients with severe HS.
Methods
We conducted a phase II clinical trial of etanercept (50 mg/wk subcutaneously) in patients with moderate to severe HS. Efficacy was measured using a Physician Global Assessment and several secondary physician- and patient-reported outcome measures. Responders were classified as those achieving at least a 50% reduction on the Physician Global Assessment score at week 12 compared with baseline.
Results
Only 3 of the 15 patients who entered the study were classified as responders (response rate of 20%; 95% confidence interval: 4.3-48.1) based on the intention-to-treat analysis. Dermatology Life Quality Index scores improved slightly from a median of 19 to 15 (P = .02). Comparison of baseline with week-12 Physician Global Assessment scores, and secondary outcome measures of lesion counts and patient pain scores, failed to show statistically significant improvement. Etanercept was generally well tolerated; however, two patients discontinued the study as a result of skin infections at the site of hidradenitis lesions requiring oral antibiotics.
Limitations
Lack of a control group and a small number of participants are limitations.
Conclusions
Our study demonstrated minimal evidence of clinically significant efficacy of etanercept (50 mg/wk subcutaneously) in the treatment of hidradenitis. Future studies using higher doses of etanercept are indicated; however, patients need to be carefully monitored for infection and other adverse events. Randomized, controlled trials will be necessary to demonstrate the risk-to-benefit ratio of tumor necrosis factor-α inhibitors in the treatment of hidradenitis.
Key words: clinical trial, efficacy, etanercept, hidradenitis suppurativa, quality of life, safety, tumor necrosis factor inhibitor
Abbreviations used: AT, as treated, BMI, body mass index, DLQI, Dermatology Life Quality Index, HS, hidradenitis suppurativa, ITT, intention to treat, PGA, Physician Global Assessment, SC, subcutaneously, TNF, tumor necrosis factor
Supported by an unrestricted grant from Amgen and grant K23AR051125 from the National Institute of Arthritis, Musculoskeletal, and Skin Diseases (Dr Gelfand).
Disclosure: Dr Gelfand has received grant support from Amgen and Centocor, and is a consultant to Amgen, Abbott, Centocor, Genentech, and Astellas. Drs Lee, Treat, Sciacca-Kirby, Chachkin, Leyden, and Vittorio, Ms Dommasch, Ms Williams, and Mr Shin have no conflicts of interest to declare.
PII: S0190-9622(08)02470-5
doi:10.1016/j.jaad.2008.11.898
© 2008 American Academy of Dermatology, Inc. Published by Elsevier Inc All rights reserved.
Volume 60, Issue 4 , Pages 565-573, April 2009

