For clinicians · Medication guide

TNF inhibitors

anti-TNF, adalimumab, etanercept, infliximab, certolizumab, golimumab

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Bottom linebDMARD class blocking TNF, used for inadequate response to csDMARDs across RA, PsA, and axSpA, effective across musculoskeletal and skin domains. Positioning to be sourced.

Dosing and administration[3]

Given subcutaneously, or intravenously for infliximab and the IV golimumab formulation. The doses below are the standard approved rheumatoid arthritis doses; several are commonly combined with methotrexate. Screen for latent tuberculosis and viral hepatitis before starting.

AgentRouteDose and frequency
Adalimumab (Humira and biosimilars)Subcutaneous40 mg every 2 weeks (some indications allow weekly dosing if not on methotrexate).
Etanercept (Enbrel and biosimilars)Subcutaneous50 mg once weekly, or 25 mg twice weekly.
Certolizumab pegol (Cimzia)Subcutaneous400 mg at weeks 0, 2, and 4 (loading), then 200 mg every 2 weeks or 400 mg every 4 weeks.
Golimumab (Simponi)Subcutaneous (IV form available)50 mg once monthly subcutaneously; the intravenous form is 2 mg/kg at weeks 0 and 4, then every 8 weeks.
Infliximab (Remicade and biosimilars)Intravenous infusion3 mg/kg at weeks 0, 2, and 6, then every 8 weeks, usually with methotrexate; may be escalated in dose or frequency.

Onset. Onset over about 2 to 12 weeks.

Doses shown are the standard approved rheumatoid arthritis doses from the respective Health Canada product monographs; regimens differ for other indications such as psoriatic arthritis and axial spondyloarthritis.

Monitoring

Contraindications

Key interactions

Clinical notes

Common side effects

Injection-site or infusion reactions; increased infection risk. Not sourced on this draft.

Tests and monitoring

Before starting, screen for latent tuberculosis (a tuberculin skin test or an interferon-gamma release assay, with IGRA preferred after prior BCG vaccination; induration of 5 mm or more is a positive skin test) and for hepatitis B where risk factors are present, and obtain baseline complete blood count, liver transaminases, and serum creatinine. Give indicated killed or inactivated vaccines, including pneumococcal and influenza, before starting where possible; live vaccines are not recommended during treatment. ACR does not set a fixed on-treatment laboratory interval for this class and lists biologic laboratory monitoring as an evidence gap, so ongoing monitoring follows the product monograph. Recommendations derived for rheumatoid arthritis.[1, 2]

Important cautions

Caution with a history of serious or recurrent infection, demyelinating disease, and certain heart failure; live-vaccine and peri-operative timing apply. To confirm from primary sources.

+Reproductive health. Pregnancy, breastfeeding, and paternal guidance for this agent is maintained on the same record and is verified separately.

References

  1. Saag KG, Teng GG, Patkar NM, et al. American College of Rheumatology 2008 recommendations for the use of nonbiologic and biologic disease-modifying antirheumatic drugs in rheumatoid arthritis. Arthritis Rheum. 2008;59(6):762-784. doi:10.1002/art.23721 https://doi.org/10.1002/art.23721
  2. Singh JA, Saag KG, Bridges SL Jr, et al. 2015 American College of Rheumatology Guideline for the Treatment of Rheumatoid Arthritis. Arthritis Care Res. 2016;68(1):1-25. doi:10.1002/acr.22783 (published simultaneously in Arthritis & Rheumatology) https://doi.org/10.1002/acr.22783
  3. Standard approved rheumatoid arthritis doses from the respective Health Canada product monographs: adalimumab (Humira), etanercept (Enbrel), certolizumab pegol (Cimzia), golimumab (Simponi), and infliximab (Remicade and biosimilars). https://health-products.canada.ca/dpd-bdpp/