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Infliximab improves signs and symptoms of psoriatic arthritis: results of the IMPACT 2 trial
  1. C Antoni1,
  2. G G Krueger2,
  3. K de Vlam3,
  4. C Birbara4,
  5. A Beutler5,
  6. C Guzzo5,
  7. B Zhou5,
  8. L T Dooley5,
  9. A Kavanaugh6,
  10. for the IMPACT 2 investigators
  1. 1Friedrich Alexander University of Erlangen-Nürnberg, Erlangen, Germany
  2. 2University of Utah Health Sciences Center, Salt Lake City, UT, USA
  3. 3University Hospital Leuven, Leuven, Belgium
  4. 4University of Massachusetts School of Medicine, Worcester, MA, USA
  5. 5Centocor, Inc, Malvern, PA, USA
  6. 6Division of Rheumatology, Allergy, and Immunology, University of California San Diego, La Jolla, CA, USA
  1. Correspondence to:
    Dr A Kavanaugh
    Center for Innovative Therapy, Division of Rheumatology, Allergy and Immunology, University of California at San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0943, USA; akavanaughucsd.edu

Abstract

Objectives: To evaluate further in a phase III, double blind trial the efficacy of infliximab in patients with active psoriatic arthritis (PsA), as observed in the smaller IMPACT trial.

Methods: 200 patients with active PsA unresponsive to previous treatment were randomised to infusions of infliximab 5 mg/kg or placebo at weeks 0, 2, 6, 14, and 22. Patients with inadequate response entered early escape at week 16. The primary measure of clinical response was ACR20. Other measures included Psoriatic Arthritis Response Criteria (PsARC), Psoriasis Area and Severity Index (PASI), and dactylitis and enthesopathy assessments.

Results: At week 14, 58% of patients receiving infliximab and 11% of those receiving placebo achieved an ACR20 response and 77% of infliximab patients and 27% of placebo patients achieved PsARC (both p<0.001). Among the 85% of patients with at least 3% body surface area psoriasis involvement at baseline, 53/83 (64%) patients receiving infliximab had at least 75% improvement in PASI compared with 2/87 (2%) patients receiving placebo at week 14 (p<0.001). These therapeutic effects were maintained through the last evaluation (week 24). Fewer infliximab patients than placebo patients had dactylitis at week 14 (18% v 30%; p = 0.025) and week 24 (12% v 34%; p<0.001). Fewer infliximab patients (22%) than placebo patients (34%) had active enthesopathy at week 14 (p = 0.016); corresponding figures at week 24 were 20% and 37% (p = 0.002). Infliximab was generally well tolerated, with a similar incidence of adverse events in each group.

Conclusions: Infliximab 5 mg/kg through 24 weeks significantly improved active PsA, including dactylitis and enthesopathy, and associated psoriasis.

  • ACR, American College of Rheumatology
  • AEs, adverse events
  • ALT, alanine aminotransferase
  • ANA, antinuclear antibody
  • AST, aspartate aminotransferase
  • BSA, body surface area
  • CRP, C reactive protein
  • DMARDs, disease modifying antirheumatic drugs
  • dsDNA, double stranded DNA
  • HAQ, Health Assessment Questionnaire
  • MTX, methotrexate
  • NSAIDs, non-steroidal anti-inflammatory drugs
  • PASI, Psoriasis Area and Severity Index
  • PsA, psoriatic arthritis
  • PsARC, Psoriatic Arthritis Response Criteria
  • RA, rheumatoid arthritis
  • SF-36, Short Form-36
  • TNFα, tumour necrosis factor α, VAS, visual analogue scale
  • psoriatic arthritis
  • tumour necrosis factor α
  • infliximab
  • dactylitis
  • enthesopathy
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Supplementary materials

  • Files in this Data Supplement:

    • view PDF - Infliximab migliora segni e sintomi dell�artrite psoriasica: risultati dello studio IMPACT 2.

Footnotes

  • Published Online First 27 January 2005

  • Investigators for the Infliximab Multinational Psoriatic Arthritis Controlled Trial (IMPACT) 2 study include:USA: Dr C Birbara, Worcester, Massachusetts; Dr EP Boling, Upland, California; Dr C Codding, Oklahoma City, Oklahoma; Dr JJ Fiechtner, Lansing, Michigan; Dr RM Fleischmann, Dallas, Texas; Dr SI Goodman, Delray Beach, Florida; Dr AB Gottlieb, New Brunswick, New Jersey; Dr DG Halter, Houston, Texas; Dr JL Harshbarger, Wilmington, North Carolina; Dr K Hobbs, Denver, Colorado; Dr A Kavanaugh, La Jolla, California; Dr SM Lourie, Greenbelt, Maryland; Dr P Mease, Seattle, Washington; Dr A Menter, Dallas, Texas; Dr DM Pariser, Norfolk, Virginia; Dr WJ Shergy, Huntsville, Alabama; Dr EL Siegel, Wheaton, Maryland; Dr ME Wenger, Lancaster, Pennsylvania; Dr DJ Wallace, Los Angeles, California.Canada: Dr R Bissonnette, Montreal, Quebec; Dr J Carter Thorne, New Market, Ontario; Dr D Gladman, Toronto, Ontario; Dr E Keystone, Toronto, Ontario; Dr W Gulliver, St John’s, New Foundland; Dr K Papp, Waterloo, Ontario; Dr Y Poulin, Quebec, Quebec; Dr L Rosoph, North Bay, Ontario.Germany: Dr C Antoni, Erlangen; Dr GR Burmester, Berlin; Dr C Fiehn, Heidelberg; Dr J Sieper, Berlin; Dr J Wollenhaupt, Hamburg.Belgium: Dr P Geusens, Diepenbeek; Dr R Westhovens, Leuven.United Kingdom: Dr P Emery, Leeds; Dr B Kirkham, London.

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