Document Server@UHasselt >
Research >
Research publications >

Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/4102

Title: Infliximab inhibits progression of radiographic damage in patients with active psoriatic arthritis through one year of treatment - Results from the induction and maintenance psoriatic arthritis clinical trial 2
Authors: VAN DER HEIJDE, Desiree
Kavanaugh, A.
Gladman, D. D.
Antoni, C.
Krueger, G. G.
Guzzo, C.
Zhou, B.
Dooley, L. T.
de Vlam, K.
Birbara, C.
Halter, D.
Beutler, A.
Issue Date: 2007
Publisher: WILEY-LISS
Citation: ARTHRITIS AND RHEUMATISM, 56(8). p. 2698-2707
Abstract: Objective. To evaluate the effect of infliximab on progression of structural damage over I year in patients with active psoriatic arthritis (PsA) enrolled in the Induction and Maintenance Psoriatic Arthritis Clinical Trial 2. Methods. In this double-blind, placebo-controlled study, 200 patients with active PsA were randomly assigned (1:1 ratio) to receive infusions of infliximab (5 mg/kg) or placebo at weeks 0, 2, and 6, and every 8 weeks thereafter through week 54. At week 24, patients initially assigned to receive placebo crossed over to receive infliximab (5 mg/kg). Based on predefined criteria, patients randomized to receive placebo could enter early escape by receiving infliximab (5 mg/kg) starting at week 16, and patients randomized to receive infliximab could have the dose increased to 10 mg/kg starting at week 38. Patients were analyzed according to the treatment they were randomized to receive. Radiographs of hands and feet were obtained at baseline and at weeks 24 and 54. Two readers blinded to treatment assignment and radiograph sequence independently evaluated erosions and joint space narrowing using the Sharp/VAN DER HEIJDE scoring method modified for PsA. Results. At week 24, patients randomized to receive infliximab 5 mg/kg had significantly less radiographic progression compared with patients randomized to receive placebo, with mean +/- SD changes from baseline in the total Sharp/VAN DER HEIJDE score of -0.70 +/- 2.53 and 0.82 +/- 2.62, respectively (P < 0.001). At week 54, mean SD changes from baseline in the total Sharp/VAN DER HEIJDE score were -0.94 +/- 3.40 in patients randomized to receive infliximab and 0.53 2.60 in those receiving placebo/infliximab (P = 0.001). Conclusion. Infliximab significantly inhibits radiographic progression in patients with PsA as early as 6 months after starting treatment, and the beneficial effect continues through I year of infliximab therapy.
Notes: Leiden Univ, Med Ctr, Leiden, Netherlands. Univ Calif San Diego, San Diego, CA 92103 USA. Univ Toronto, Toronto, ON, Canada. Schering Plough Corp, Kenilworth, NJ 07033 USA. Univ Utah, Hlth Sci Ctr, Salt Lake City, UT USA. Centocor Inc, Malvern, PA 19355 USA. Katholieke Univ Leuven Hosp, Louvain, Belgium. Univ Hasselt, Diepenbeek, Belgium. Univ Hosp, Maastricht, Netherlands. Univ Massachusetts, Sch Med, Worcester, MA 01605 USA. Houston Clin Res, Houston, TX USA.VAN DER HEIJDE, D, Korte Raarberg 46, NL-6231 KR Meersen, Netherlands.d.vanderheijde@kpnplanet.nl
URI: http://hdl.handle.net/1942/4102
Link to publication: http://doi.wiley.com/10.1002/art.22805
ISI #: 000248629900025
ISSN: 0004-3591
Category: A1
Type: Journal Contribution
Validation: ecoom, 2008
Appears in Collections: Research publications

Files in This Item:

There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.