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. 2000 Nov;59(Suppl 1):i46–i49. doi: 10.1136/ard.59.suppl_1.i46

Etanercept (Enbrel): update on therapeutic use

G Spencer-Green
PMCID: PMC1766625  PMID: 11053088

Abstract

Tumour necrosis factor (TNF) is an important inflammatory disease mediator in a wide spectrum of articular diseases, including adult and juvenile rheumatoid arthritis (RA, JRA). Etanercept (Enbrel), approved in the United States and in Europe for use in patients with RA and JRA, is an effective inhibitor of TNF that has been shown to provide rapid and sustained improvement in both of these diseases. Long term studies continue to show that etanercept controls signs and symptoms of RA and JRA with no change in rate or type of adverse event over time. To demonstrate that etanercept is effective as first line treatment for patients with early active RA who have not been previously treated with methotrexate, and to examine the effect of etanercept on radiographic progression, a double blind, placebo controlled study was recently conducted, comparing etanercept with methotrexate (median dose 20 mg per week). Both etanercept 25 mg twice weekly and rapidly escalated methotrexate were effective in reducing the signs and symptoms of RA, and etanercept was significantly better than methotrexate in slowing the rate of radiographic erosions. In patients with severe psoriatic arthritis (PsA), a double blind, placebo controlled study demonstrated that etanercept was also effective in reducing disease activity in PsA. Etanercept has been well tolerated in all of these clinical trials and offers an important new treatment option to patients with inflammatory articular diseases.



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Figure 1  .

Figure 1  

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The change from baseline over time in the Disease Activity Score (DAS). Improvement in the etanercept 25 mg group was more rapid than the methotrexate group.

Figure 2  .

Figure 2  

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The area under the curve (AUC) of the change from baseline in the Disease Activity Score (DAS). Improvement in the etanercept 25 mg group was significantly better than the methotrexate group over both the six and 12 month time periods (p = 0.002 and p = 0.031, respectively).

Figure 3  .

Figure 3  

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Box plot showing change from baseline in erosion score at one year for patients receiving etanercept 25 mg and methotrexate. The median change for each was 0. The difference between the etanercept 25 mg and the methotrexate groups was statistically significant (p = 0.002).

Figure 4  .

Figure 4  

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Box plot showing change from baseline in Total Sharp Score at one year for patients receiving etanercept and methotrexate. The median change for each was 0. The difference between the etanercept 25 mg and the methotrexate groups did not meet statistical significance (p = 0.110).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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