Etanercept is a genetically engineered protein that slows or stops
rheumatoid arthritis inflammation and joint damage. It has been studied and
approved for use in treatment of children ages 4 to 17 who
have juvenile rheumatoid arthritis (JRA).
Rheumatoid arthritis inflammation is caused in part by a substance
called tumor necrosis factor (TNF) in the joint area; etanercept deactivates
TNF.1
Etanercept is used to treat moderate to severe rheumatoid arthritis
symptoms and to prevent joint damage, particularly in people who have had side
effects or poor results from methotrexate treatment.
When first approved for use, etanercept treatment was used only
after methotrexate treatment had been unsuccessful. However, recent research
suggests that etanercept works more quickly and more effectively prevents joint
damage than methotrexate. (Long-term studies have yet to confirm whether
etanercept prevents joint damage over a number of years.) As a result, the
U.S. Food and Drug Administration (FDA) has approved
etanercept for treating early stages of the disease.2
It may be a treatment option for a child who has not responded to nonsteroidal
anti-inflammatory drugs (NSAIDs).
Etanercept has shown positive preliminary results as a treatment
for
JRA-related inflammatory eye disease when combined
with methotrexate and corticosteroid eyedrops.3
Improves joint pain and swelling as soon as 2
weeks from the beginning of treatment.
In a recent preliminary
study, etanercept improved symptoms in 80% of children with
polyarticular JRA (polyarthritis). This improvement
was maintained for 2 years after treatment began.4 In
another study of children with severe, long-standing polyarticular JRA who have
not been helped by methotrexate, etanercept provided symptom improvement that
was sustained for at least 2 years (the period of the study).5
Has shown promising results in safely improving
vision in a small sample of children with JRA-related inflammatory eye disease
(uveitis).3
May
not be an effective treatment for a child with
systemic JRA.6
Side effects of etanercept are usually minimal, including:6
Irritation and redness at the injection
site.
Runny nose and cough (upper respiratory
infection).
Headache.
Gastrointestinal symptoms.
Rash.
Etanercept suppresses the
immune system, making it difficult for the body to
fight infection. Therefore, etanercept cannot be given to a person with an
active viral or bacterial infection, nor within 3 months of a live-virus
vaccine. If your child develops a sore throat, cough, fever, or skin or bladder
infection, contact your child's health professional immediately.
Etanercept can reactivate tuberculosis (TB) in people who have been
previously infected with TB. Before starting etanercept treatment, your child
should be screened for tuberculosis.7
Screening is usually done with a tuberculin skin test and possibly a
chest X-ray.
See Drug Reference for a full list of side effects. (Drug Reference
is not available in all systems.)
Bathon JM, et al. (2000). A comparison of etanercept
and methotrexate in patients with early rheumatoid arthritis. New England Journal of Medicine, 343(22):
1586–1593.
Klippel JH (2000). Biologic therapy for rheumatoid
arthritis. New England Journal of Medicine, 343(22):
1640–1641.
Reiff A, et al. (2001). Etanercept therapy in children
with treatment-resistant uveitis. Arthritis and
Rheumatism, 44(6): 1411–1415.
Culy CR, Keating GM (2003). Spotlight on etanercept in
rheumatoid arthritis, psoriatic arthritis, and juvenile rheumatoid arthritis.
Biodrugs, 17(2): 139–145.
Lovell DJ, et al. (2003). Long-term efficacy and
safety of etanercept in children with polyarticular-course juvenile rheumatoid
arthritis. Arthritis and Rheumatism, 48(1):
218–226.
Wargula JC, Lovell DJ (2000). Use of etanercept in
children. Bulletin on the Rheumatic Diseases, 49(12):
1–4.
Pisetsky DS, St Clair EW (2001). Progress in the
treatment of rheumatoid arthritis. JAMA, 286(22):
2787–2790.
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