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Two year maintenance of efficacy and safety of infliximab in the treatment of ankylosing spondylitis
  1. J Braun1,2,
  2. J Brandt2,
  3. J Listing3,
  4. A Zink3,
  5. R Alten4,
  6. G Burmester5,
  7. E Gromnica-Ihle6,
  8. H Kellner7,
  9. M Schneider8,
  10. H Sörensen9,
  11. H Zeidler10,
  12. J Sieper1,3
  1. 1University Medicine Berlin, Campus Benjamin Franklin, Germany
  2. 2Rheumatology Medical Centre Ruhrgebiet, Herne, Germany
  3. 3German Rheumatism Research Centre, Berlin, Germany
  4. 4Schlosspark Clinic, Berlin, Germany
  5. 5Charité Hospital, Humboldt University, Berlin, Germany
  6. 6Berlin-Buch Hospital, Berlin Germany
  7. 7Ludwig-Maximilians-University, Munich, Germany
  8. 8Heinrich-Heine-University, Düsseldorf, Germany
  9. 9Immanuel Hospital, Berlin, Germany
  10. 10Medical University, Hannover, Germany
  1. Correspondence to:
    Professor J Braun
    Rheumazentrum Ruhrgebiet, Landgrafenstr 15, 44652 Herne, Germany;


Objective: To obtain results of the second year extension of an original 3 month randomised, placebo controlled trial (and the 1 year extension study) assessing the use of infliximab, a monoclonal antibody to tumour necrosis factor α, for the treatment of patients with ankylosing spondylitis (AS).

Methods: Of the 54 patients with AS who completed the first year of the study, 52 continued to receive infliximab 5 mg/kg every 6 weeks up to week 102. The primary end point was the proportion of patients achieving at least 50% improvement from baseline in the Bath AS Disease Activity Index (BASDAI) at week 102. Other assessments included patient and physician global assessments, quality of life as assessed by Short Form-36, Bath AS Functional Index, Bath AS Metrology Index, and C reactive protein (CRP).

Results: Improvement in signs and symptoms of AS seen during the first year of the study was sustained during the second year. Forty nine patients (71% of 69 enrolled patients and 49/52 (94%) patients who started year 2) completed the study up to week 102. Thirty (58%) patients achieved at least 50% improvement from baseline in the BASDAI score at week 102. Scores for other efficacy assessments were similar at weeks 54 and 102. Median CRP levels remained low at weeks 54 and 102 (3.9 and 4.3 mg/l, respectively). Side effects during the second year of the study were similar to those of the first year of treatment with infliximab.

Conclusions: Patients with AS treated for 2 years with infliximab 5 mg/kg exhibited a good and durable clinical response.

  • AS, ankylosing spondylitis
  • ASAS, Assessment in Ankylosing Spondylitis
  • BASDAI, Bath Ankylosing Spondylitis Disease Activity Index
  • BASFI, Bath AS Functional Index
  • BASMI, Bath AS Metrology Index
  • CRP, C reactive protein
  • DMARDs, disease modifying antirheumatic drugs
  • ESR, erythrocyte sedimentation rate
  • ITT, intention to treat
  • NSAIDs, non-steroidal anti-inflammatory drugs
  • SF-36, Short Form-36
  • TNFα, tumour necrosis factor α
  • tumour necrosis factor α
  • ankylosing spondylitis
  • infliximab

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  • The first two authors contributed equally to this paper.