4.7 Article

Serious infection risk after 1 year between patients with rheumatoid arthritis treated with rituximab or with a second TNFi after initial TNFi failure: results from The British Society for Rheumatology Biologics Register for Rheumatoid Arthritis

期刊

RHEUMATOLOGY
卷 57, 期 9, 页码 1533-1540

出版社

OXFORD UNIV PRESS
DOI: 10.1093/rheumatology/kex304

关键词

Rituximab; TNF inhibitors; safety of biologics; second line biologic treatment; observational cohort; serious infections

资金

  1. Abbott Laboratories
  2. Pfizer
  3. Roche
  4. UCB Pharma
  5. Arthritis Research UK Centre for Epidemiology [20380]
  6. Instituto de Salud Carlos III (Spain)
  7. Articulum Fellowship

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Objectives. Both TNF inhibitors (TNFi) and rituximab (RTX), a B-cell depleting biologic, can disrupt the immune system in RA. RTX is licensed in Europe for use following TNFi failure. However, safety data on serious infections (SIs) are scarce for RTX in daily practice. This analysis aims to compare the risk of SIs in the first year after a switch to either TNFi or RTX in patients who have failed a first TNFi. Methods. This study included patients with RA registered with the British Society for Rheumatology Biologics Register (BSRBR-RA) who switched to either a second TNFi or RTX after failing a first TNFi. Patients were followed until first SI, treatment discontinuation, last recorded follow-up or the end of the first year after the switch, whichever came first. SI was defined as requiring hospitalization, intravenous antibiotics or resulting in death. The risk of first SI was compared between TNFi and RTX using Cox proportional hazard models adjusted using propensity scores using inverse probability of treatment weighting. Results. This analysis included 3419 TNFi and 1396 RTX patients contributing 2765 and 1224 personyears (pyrs), respectively. SI occurred in 164 (4.8%) TNFi and 81 (5.8%) RTX patients giving a crude rate of 59 and 66 SI/1000 pyrs, respectively. The adjusted hazard ratio for SI was 1.0 (95% CI: 0.7, 1.4). Conclusion. The risk of SIs was comparable over the first year of treatment between TNFi and RTX treatment in patients who had failed a single prior TNFi.

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