Gut 2006;55:505-509
INFLAMMATORY BOWEL DISEASE
Infliximab for the treatment of pyoderma gangrenosum: a randomised, double blind, placebo controlled trial
1 Bristol Royal Infirmary, Bristol, UK
2 St Marks Hospital, Harrow, UK
3 The Dermatology Centre, Hope Hospital, The University of Manchester, Manchester, UK
Correspondence to:
Dr C S Probert
Bristol Royal Infirmary, Bristol BS2 8HW, UK; c.s.j.probert{at}bristol.ac.uk
Background: Pyoderma gangrenosum (PG) is a chronic ulcerating skin condition that often occurs in association with inflammatory bowel disease. There have been a number of reports of PG responding to infliximab, a monoclonal antibody against tumour necrosis factor
.
Aim: In the first randomised placebo controlled trial of any drug for the treatment of PG, we have studied the role of infliximab in this disorder.
Subjects: Patients 18 years of age or older with a clinical diagnosis of PG were invited to take part.
Methods: Patients were randomised to receive an infusion of infliximab at 5 mg/kg or placebo at week 0. Patients were then assessed at week 2 and non-responders were offered open labelled infliximab. The primary end point was clinical improvement at week 2, with secondary end points being remission and improvement at week 6.
Results: Thirty patients were entered into the study. After randomisation, 13 patients received infliximab and 17 patients received placebo. At week 2, significantly more patients in the infliximab group had improved (46% (6/13)) compared with the placebo group (6% (1/17); p = 0.025). Overall, 29 patients received infliximab with 69% (20/29) demonstrating a beneficial clinical response. Remission rate at week 6 was 21% (6/29). There was no response in 31% (9/29) of patients.
Conclusions: This study has demonstrated that infliximab at a dose of 5 mg/kg is superior to placebo in the treatment of PG. Open label treatment with infliximab also produced promising results. Infliximab treatment should be considered in patients with PG.
Abbreviations: PG, pyoderma gangrenosum; IBD, inflammatory bowel disease; TNF-
, tumour necrosis factor
; DLQI, dermatology life quality index
Keywords: pyoderma gangrenosum; infliximab; inflammatory bowel disease
Relevant Article
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
Gut 2006 55: 437.
This article has been cited by other articles:
-
Eaton, P. A., Callen, J. P.
(2009). Mycophenolate Mofetil as Therapy for Pyoderma Gangrenosum. Arch Dermatol
145: 781-785
[Abstract] [Full Text] -
Edwards, M. H., Leak, A. M.
(2009). Pericardial effusions on anti-TNF therapy for rheumatoid arthritis--a drug side effect or uncontrolled systemic disease?. Rheumatology (Oxford)
48: 316-317
[Full Text] -
Furst, D E, Breedveld, F C, Kalden, J R, Smolen, J S, Burmester, G R, Sieper, J, Emery, P, Keystone, E C, Schiff, M H, Mease, P, van Riel, P L C M, Fleischmann, R, Weisman, M H, Weinblatt, M E
(2007). Updated consensus statement on biological agents for the treatment of rheumatic diseases, 2007. Ann Rheum Dis
66: iii2-iii22
[Full Text] -
Brooklyn, T., Dunnill, G., Probert, C.
(2006). Diagnosis and treatment of pyoderma gangrenosum. BMJ
333: 181-184
[Full Text] -
(2006). Infliximab Is Effective for Pyoderma Gangrenosum with or without Inflammatory Bowel Disease. Journal Watch Dermatology
2006: 5-5
[Full Text]
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.
