Literature DB >> 22356632

Effective and sustainable biologic treatment of psoriasis: what can we learn from new clinical data?

R G Langley1.   

Abstract

The introduction of the biologic agents, adalimumab, etanercept, infliximab and ustekinumab, has provided more options for the short- and long-term treatment of patients with psoriasis. Physicians are now able to achieve and maintain effective disease control in more patients using biologic therapies. Newly published clinical data support the introduction of novel optimization strategies to further improve outcomes in patients with psoriasis. Recent randomized controlled clinical trials have provided data on the efficacy of conventional therapies, including systemic agents, and biologics at specific time points. Switching from methotrexate to a tumour necrosis factor (TNF)-α antagonist after 16 weeks can improve response rates, as demonstrated in a study of patients with moderate-to-severe psoriasis, while the benefit of long-term methotrexate use remains unclear. In a separate study, psoriasis area and severity index (PASI) ≥ 75 response rates were maintained over time (>3 years for adalimumab), suggesting that long-term biologic therapy is an effective and sustainable treatment option for psoriasis. For each individual patient, the benefit of a particular treatment needs to be balanced with the risks. The lack of head-to-head trials of antipsoriatic therapies, particularly biologic therapies, does not help with making individualized treatment decisions. However, a benefit-risk assessment of TNF-α antagonists calculated from an integrated analysis of published literature in moderate-to-severe psoriasis can be used to aid clinical practice. The number needed to treat, number needed to harm and number of patient years of observation to detect an adverse event have been determined for adalimumab, etanercept and infliximab. The benefit-risk profiles generated demonstrated that, during the initial year of treatment, likelihood of success with TNF-α antagonists was several orders of magnitude greater than the likelihood of serious toxicity.
© 2012 The Author. Journal of the European Academy of Dermatology and Venereology © 2012 European Academy of Dermatology and Venereology.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22356632     DOI: 10.1111/j.1468-3083.2011.04412.x

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN: 0926-9959            Impact factor:   6.166


  3 in total

1.  Clinical improvement in psoriasis with specific targeting of interleukin-23.

Authors:  Tamara Kopp; Elisabeth Riedl; Christine Bangert; Edward P Bowman; Elli Greisenegger; Ann Horowitz; Harald Kittler; Wendy M Blumenschein; Terrill K McClanahan; Thomas Marbury; Claus Zachariae; Danlin Xu; Xiaoli Shirley Hou; Anish Mehta; Anthe S Zandvliet; Diana Montgomery; Frank van Aarle; Sauzanne Khalilieh
Journal:  Nature       Date:  2015-03-09       Impact factor: 49.962

2.  Annual biologic treatment cost for new and existing patients with moderate to severe plaque psoriasis in Greece.

Authors:  Vassilis Fragoulakis; Efklidis Raptis; Elli Vitsou; Nikolaos Maniadakis
Journal:  Clinicoecon Outcomes Res       Date:  2015-01-08

Review 3.  An evolution in switching therapy for psoriasis patients who fail to meet treatment goals.

Authors:  Francisco Kerdel; Martin Zaiac
Journal:  Dermatol Ther       Date:  2015-08-10       Impact factor: 2.851

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.