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Efficacy of B cell depletion in patients with rheumatoid arthritis refractory to anti-tumour necrosis factor α agents: an open-label observational study
  1. L Brulhart1,
  2. A Ciurea2,
  3. A Finckh1,
  4. A Notter2,
  5. J M Waldburger1,
  6. D Kyburz2,
  7. C Gabay1
  1. 1Division of Rheumatology, University Hospital of Geneva, Geneva, Switzerland
  2. 2Rheumaklinik, University Hospital of Zurich, Zurich, Switzerland
  1. Correspondence to:
    C Gabay
    Division of Rheumatology, University Hospital of Geneva, 26 Avenue Beau-Séjour, 1211 Geneva 14, Switzerland; cem.gabay{at}

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About 30% of patients with rheumatoid arthritis fail to achieve a marked clinical response to tumour necrosis factor (TNF)α inhibitors.1 Rituximab, a chimeric monoclonal antibody, selectively depletes human CD20-positive B cells.2 In patients with rheumatoid arthritis with incomplete response to methotrexate (MTX), response with the addition of rituximab was superior to that with MTX alone.3 We carried out an observational study to assess the efficacy and safety of selective B cell depletion in the management of patients with rheumatoid arthritis refractory to TNFα inhibitors.

Ten patients fulfilling the 1987 American College of Rheumatology diagnostic criteria for rheumatoid arthritis4 and refractory to at least one anti-TNF agent for ⩾3 months were prospectively enrolled. Table 1 presents their clinical characteristics at baseline. All of them had active disease (median Disease Activity Score (DAS28) 5.28, interquartile range (IQR): 4.6–6.3).5

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Table 1

 Baseline clinical and laboratory characteristics …

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  • Published Online First 15 March 2006

  • Competing interests: None declared.

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