S'abonner

Achievement of the National Psoriasis Foundation treatment targets with ixekizumab: Pooled analyses from 4 clinical studies - 08/07/21

Doi : 10.1016/j.jaad.2019.09.030 
April Armstrong, MD, MPH a, , David Amato, DO b, William Huster, PhD b, Clement Ojeh, PhD c, Abby S. Van Voorhees, MD d
a Department of Dermatology, Keck School of Medicine of USC, University of Southern California, Los Angeles, California 
b Eli Lilly and Company, Indianapolis, Indiana 
c Lilly USA, Indianapolis, Indiana 
d Department of Dermatology, Eastern Virginia Medical School, Norfolk, Virginia 

Correspondence to: April W. Armstrong, MD, MPH, Office of the Dean, Keck School of Medicine of USC, 1975 Zonal Ave, Los Angeles, CA 90033.Office of the DeanKeck School of Medicine of USC1975 Zonal AveLos AngelesCA90033

Abstract

Background

The National Psoriasis Foundation (NPF) published treatment targets for US patients with plaque psoriasis. However, data are lacking on how well existing therapies help achieve these goals.

Objective

To examine the ability of an interleukin 17 inhibitor, ixekizumab, in achieving these treatment targets.

Methods

Post hoc analysis was performed on pooled data from 4 phase III clinical trials assessing ixekizumab for plaque psoriasis: the UNCOVER-1, -2, and -3 trials and the IXORA-S trial. Treatment response was evaluated using the NPF-defined acceptable response (affected body surface area [BSA] of 3% or less or BSA improvement of 75% or higher at 12 weeks of treatment) and target response (BSA of 1% or less at 12 weeks and every 6 months thereafter).

Results

In the UNCOVER trials (n = 2701), acceptable and target response rates at week 12 were 73.9% and 51.8% with ixekizumab 80 mg every 2 weeks, 35.7% and 14.9% with etanercept 50 mg, and 3.0% and 0.6% with placebo, respectively. In the IXORA-S trial (n = 302), acceptable and target response rates at week 12 were significantly higher with ixekizumab every 2 weeks versus ustekinumab (acceptable response 68.4% vs 38.6%, P < .0001; target response 50.7% vs 24.1%, P < .0001).

Limitations

Data were from controlled studies and may not reflect real-world practice.

Conclusion

The majority of patients treated with ixekizumab in 4 phase III clinical trials achieved NPF, patient-centered treatment targets.

Le texte complet de cet article est disponible en PDF.

Key words : etanercept, interleukin 17, ixekizumab, National Psoriasis Foundation, pooled analysis, psoriasis, treatment goals

Abbreviations used : BSA, NPF, PASI, sPGA


Plan


 Funding sources: Supported by Eli Lilly and Company.
 Presentation: “Achievement of the National Psoriasis Foundation Treatment Targets Among Patients in Ixekizumab Clinical Trials: Analysis of Pooled UNCOVER Results” was presented at the National Psoriasis Foundation 2017 Research Symposium, Chicago, Illinois, August 3-5, 2017.
 Conflicts of interest: Dr Armstrong has served as an investigator and/or advisor to AbbVie, BMS, Celgene, Janssen, Novartis, Eli Lilly and Company, Leo Pharma, Regeneron, Sanofi, and Ortho Dermatologics. Dr Amato is a shareholder and former employee of Eli Lilly and Company. Drs Huster and Ojeh were employees but retired from Eli Lilly and Company. Dr Van Voorhees has received honoraria for consulting and/or participating in the advisory boards for Dermira, Novartis, Allergan, Celgene, AbbVie, DermTech, Pfizer, AstraZeneca, Corrona, and Valeant; she also served as an investigator for Celgene, Lilly, and Corrona.
 IRB approval status: The individual studies were approved by institutional review boards.
Reprints not available from the authors.


© 2021  American Academy of Dermatology, Inc.. Publié par Elsevier Masson SAS. Tous droits réservés.
Ajouter à ma bibliothèque Retirer de ma bibliothèque Imprimer
Export

    Export citations

  • Fichier

  • Contenu

Vol 85 - N° 2

P. 330-336 - août 2021 Retour au numéro
Article précédent Article précédent
  • Comparative safety of systemic immunomodulatory medications in adults with atopic dermatitis
  • Maria C. Schneeweiss, Lourdes Perez-Chada, Joseph F. Merola
| Article suivant Article suivant
  • Predictors of hepatitis B and C virus reactivation in patients with psoriasis treated with biologic agents: a 9-year multicenter cohort study
  • Hsien-Yi Chiu, Ying-Ming Chiu, Nien-Feng Chang Liao, Ching-Chi Chi, Tsen-Fang Tsai, Chang-Yu Hsieh, Tsu-Yi Hsieh, Kuo-Lung Lai, Tsu-Man Chiu, Nan-Lin Wu, Rosaline Chung-yee Hui, Chaw-Ning Lee, Ting-Shun Wang, Po-Hua Chen, Chao-Chun Yang, Yu-Huei Huang

Bienvenue sur EM-consulte, la référence des professionnels de santé.
L’accès au texte intégral de cet article nécessite un abonnement.

Déjà abonné à cette revue ?

Mon compte


Plateformes Elsevier Masson

Déclaration CNIL

EM-CONSULTE.COM est déclaré à la CNIL, déclaration n° 1286925.

En application de la loi nº78-17 du 6 janvier 1978 relative à l'informatique, aux fichiers et aux libertés, vous disposez des droits d'opposition (art.26 de la loi), d'accès (art.34 à 38 de la loi), et de rectification (art.36 de la loi) des données vous concernant. Ainsi, vous pouvez exiger que soient rectifiées, complétées, clarifiées, mises à jour ou effacées les informations vous concernant qui sont inexactes, incomplètes, équivoques, périmées ou dont la collecte ou l'utilisation ou la conservation est interdite.
Les informations personnelles concernant les visiteurs de notre site, y compris leur identité, sont confidentielles.
Le responsable du site s'engage sur l'honneur à respecter les conditions légales de confidentialité applicables en France et à ne pas divulguer ces informations à des tiers.


Tout le contenu de ce site: Copyright © 2024 Elsevier, ses concédants de licence et ses contributeurs. Tout les droits sont réservés, y compris ceux relatifs à l'exploration de textes et de données, a la formation en IA et aux technologies similaires. Pour tout contenu en libre accès, les conditions de licence Creative Commons s'appliquent.