4.3 Article

A randomized study comparing the combination of nbUVB and etanercept to etanercept monotherapy in patients with psoriasis who do not exhibit an excellent response after 12 weeks of etanercept

Journal

JOURNAL OF DERMATOLOGICAL TREATMENT
Volume 23, Issue 4, Pages 261-267

Publisher

INFORMA HEALTHCARE
DOI: 10.3109/09546634.2011.607795

Keywords

etanercept; ultraviolet B; psoriasis; tumor necrosis factor antagonist; phototherapy

Categories

Funding

  1. Amgen Canada, Inc.
  2. Wyeth, A Pfizer Company
  3. Abbott Laboratories
  4. LeoPharma
  5. Merck
  6. Pfizer
  7. Abbott
  8. Amgen
  9. Astellas
  10. Boehringer-Ingelheim
  11. Celgene
  12. Centocor
  13. Isotechnika
  14. Janssen-Ortho
  15. Merck-Serono
  16. Novartis

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Background: There is a lack of data on the combination of phototherapy with etanercept in patients who have not shown an excellent response to etanercept monotherapy. Objectives: To study the combination of narrow-band ultraviolet B (nbUVB) phototherapy with etanercept in patients not demonstrating an improvement of 90% in their Psoriasis Area Severity Index (PASI-90) after 12 weeks of etanercept. Patients and methods: Psoriatic patients not reaching PASI-90 after 12 weeks of etanercept therapy were randomized (1: 1) to receive either etanercept (50 mg once a week) monotherapy or in combination with nbUVB three times weekly for periods of 4 weeks. Results: Seventy-five patients were randomized. Only 21.6% of patients achieved adherence of 80% or more for nbUVB treatments. At week 24, PASI-90 was reached by 16.2% of patients in the etanercept plus nbUVB group when compared with 15.8% of patients in the etanercept monotherapy group (p = 1.000). In patients with high adherence to nbUVB, the PASI-90 at week 16 was 42.9% for etanercept with nbUVB when compared with 3.4% for etanercept monotherapy (p = 0.018). Both treatments were well tolerated. Conclusion: Addition of nbUVB after 12 weeks of etanercept did not significantly improve the clinical response except for a subset of patients with high adherence to nbUVB. Clinical Trials Registration number: NCT00640393.

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