Comparative effectiveness of first-line tumour necrosis factor inhibitor versus non-tumour necrosis factor inhibitor biologics and targeted synthetic agents in patients with rheumatoid arthritis: results from a large US registry study.
retrospective_cohort · Level III
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- Record sourced from PubMed, PMID 32719038.
- Also identified by DOI 10.1136/annrheumdis-2020-217209 and PMC identifier 7788059.
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Abstract
This study evaluated the comparative effectiveness of a tumour necrosis factor inhibitor (TNFi) versus a non-TNFi (biological disease-modifying antirheumatic drugs (bDMARDs) and targeted synthetic DMARDs (tsDMARDs)) as the first-line treatment following conventional synthetic DMARDs, as well as potential modifiers of response, observed in US clinical practice. Data were from a large US healthcare registry (Consortium of Rheumatology Researchers of North America Rheumatoid Arthritis Registry). The analysis included patients (aged ≥18 years) with a documented diagnosis of rheumatoid arthritis (RA), a valid baseline Clinical Disease Activity Index (CDAI) score of >2.8 and no prior bDMARD or tsDMARD use. Outcomes were captured at 1-year postinitiation of a TNFi (adalimumab, etanercept, certolizumab pegol, golimumab or infliximab) or a non-TNFi (abatacept, tocilizumab, rituximab, anakinra or tofacitinib) and included CDAI, 28-Joint Modified Disease Activity Score, patient-reported outcomes (including the Health Assessment Questionnaire Disability Index, EuroQol-5 Dimension score, sleep, anxiety, morning stiffness and fatigue) and rates of anaemia. Groups were propensity score-matched at baseline to account for potential confounding. There were no statistically significant differences observed between the TNFi and non-TNFi treatment groups for outcomes assessed, except the incidence rate ratio for anaemia, which slightly favoured the TNFi group (19.04 per 100 person-years) versus the non-TNFi group (24.01 per 100 person-years, p=0.03). No potential effect modifiers were found to be statistically significant. The findings of no significant differences in outcomes between first-line TNF versus first-line non-TNF groups support RA guidelines, which recommend individualised care based on clinical judgement and consideration of patient preferences.
Medical subject headings
- Abatacept
- Abatacept/therapeutic use
- Adalimumab
- Adalimumab/therapeutic use
- Adult
- Aged
- Antibodies, Monoclonal
- Antibodies, Monoclonal/therapeutic use
- Antibodies, Monoclonal, Humanized
- Antibodies, Monoclonal, Humanized/therapeutic use
- Antirheumatic Agents
- Antirheumatic Agents/therapeutic use
- Arthritis, Rheumatoid
- Arthritis, Rheumatoid/drug therapy
- Biological Products
- Biological Products/therapeutic use
- Certolizumab Pegol
- Certolizumab Pegol/therapeutic use
- Etanercept
- Etanercept/therapeutic use
- Female
- Humans
- Infliximab
- Infliximab/therapeutic use
- Interleukin 1 Receptor Antagonist Protein
- Interleukin 1 Receptor Antagonist Protein/therapeutic use
- Male
- Middle Aged
- Patient Reported Outcome Measures
- Piperidines
- Piperidines/therapeutic use
- Propensity Score
- Pyrimidines
- Pyrimidines/therapeutic use
- Registries
- Rituximab
- Rituximab/therapeutic use
- Treatment Outcome
- Tumor Necrosis Factor Inhibitors
- Tumor Necrosis Factor Inhibitors/therapeutic use