S'abonner

Maintenance of skin clearance with ixekizumab treatment of psoriasis: Three-year results from the UNCOVER-3 study - 15/10/18

Doi : 10.1016/j.jaad.2018.05.032 
Craig Leonardi, MD a, , Catherine Maari, MD b, c, Sandra Philipp, MD d, Orin Goldblum, MD e, Lu Zhang, MS e, Nicole Burkhardt, PhD e, Susan Ball, PhD e, Lotus Mallbris, MD, PhD e, Pablo Gonzalez, MD f, Pablo Fernández-Peñas, MD, PhD g, Luis Puig, MD, PhD h
a Central Dermatology, St. Louis, Missouri 
b Innovaderm Research Inc, Montreal, Quebec, Canada 
c Medical University of Graz, Graz, Austria 
d Charité Universitätsmedizin Berlin, Berlin, Germany 
e Eli Lilly and Company, Indianapolis, Indiana 
f Buenos Aires Skin SA, Buenos Aires, Argentina 
g Department of Dermatology, Westmead Hospital Dermatology Service, The University of Sydney, Westmead, Australia 
h Hospital de la Santa Creu i Sant Pau, Barcelona, Spain 

Reprint requests: Craig Leonardi, MD, Central Dermatology, 1034 South Brentwood Blvd, Suite 600, St. Louis, MO 63117.Central Dermatology1034 South Brentwood BlvdSuite 600St. LouisMO63117

Abstract

Background

Psoriasis is a chronic disease that may require long-term treatment. Ixekizumab (IXE), which is a high-affinity monoclonal antibody that selectively targets interleukin 17A, is an approved therapy for patients with moderate-to-severe plaque psoriasis.

Objective

To evaluate the efficacy and safety of IXE through 156 weeks from the UNCOVER-3 study in patients who were treated with the recommended dose regimen (160 mg of IXE at week 0, 80 mg every 2 weeks up to week 12, and 80 mg every 4 weeks thereafter).

Methods

Patients randomized to IXE every 2 weeks, IXE every 4 weeks, etanercept twice weekly, or placebo were switched to IXE every 4 weeks during the long-term extension period. Efficacy data were summarized by using the as-observed, multiple imputation, and modified nonresponder imputation methods.

Results

At week 156, 80.5% of patients had achieved at least a 75% improvement from baseline in their Psoriasis Area Severity Index (PASI) score, 66.0% had achived at least a 90% improvement from baseline in their PASI score, and 45.1% had achieved a 100% improvement from baseline in their PASI score with use of the modified nonresponder imputation method, and 97.2% and 86.2% of patients had achived at least a 75% improvement from baseline in their PASI score with use of the as-observed and multiple imputation methods, respectively. Similar response rates were observed in patients with baseline scalp, nail, or palmoplantar involvement. No new safety signals were identified through year 3.

Limitations

No placebo or active comparison after week 12.

Conclusion

IXE sustained high responses with clearance of skin and nail lesions, with no new safety concerns through 3 years.

Le texte complet de cet article est disponible en PDF.

Key words : efficacy, interleukin 17, ixekizumab, long-term, psoriasis, safety, UNCOVER-3

Abbreviations used : AE, IXE, LTE, MI, mNRI, PASI, sPGA, TEAE


Plan


 Funding sources: Supported by Eli Lilly and Company.
 Disclosure: Dr Leonardi is in the speakers bureaus of AbbVie, Celgene, Eli Lilly, and Novartis; he is a consultant or in the advisory board of Abbvie, Amgen, Boehringer Ingelheim, Eli Lilly, Janssen, Dermira, Pfizer, Ortho Dermatologics, Sandoz, and UCB; and he is a principal investigator for Actavis, Amgen, Boehringer Ingelheim, Celgene, Cellceutix, Coherus, Corrona, Dermira, Eli Lilly, Gelnmark, Janssen, Loe Pharma, Novartis, Novella, Pfizer, and Sandoz. Dr Maari has been an advisory board member, investigator, and/or speaker for AbbVie, Amgen, Celgene, Eli Lilly and Company, Galderma, Pfizer, Leo Pharma, Merck, Novartis, Janssen, and Tribute. Dr Philipp has received honoraria for speaker services from AbbVie, Almirall, Amgen, Biogen, BMS GmbH, Celgene, Janssen Cilag, MSD, mundipharma, Novartis, and UCB Pharma; for advisory board services from AbbVie, Biogen, Eli Lilly, Janssen Cilag, Leo Pharma, Pfizer, MSD, and Novartis; and for investigator services from AbbVie, Almirall, Amgen, Biogen, Boehringer-Ingelheim, Celgene, Dermira, Eli Lilly, GSK, Janssen Cilag, Leo Pharma, Pfizer, Maruho, MSD, Novartis, UCB Pharma, and VBL Therapeutics. Dr Gonzalez has received honoraria as speaker and/or consultant and/or investigator from AbbVie, Celgene, Eli Lilly and Company, Janssen, and Novartis. Dr Fernández-Peñas has been an advisory board member, investigator, and/or speaker for Sanofi, Merck, Sun Pharma, Novartis, Merck-Serono, Roche, Leo, Abbvie, Lilly, Celgene, UCB, Janssen, Kyowa Hakko Kirin, Arena, Galderma, Amgen, and MSD. Dr Puig has been an advisory board member, investigator, and/or speaker for Abbvie, Almirall, Amgen, Baxalta, Biogen, Boehringer Ingelheim, Celgene, Gebro, Janssen, Leo-Pharma, Lilly, Merck-Serono, MSD, Novartis, Pfizer, Regeneron, Roche, Sanofi, Sandoz, and UCB. Dr Goldblum, Ms Zhang, Dr Burkhardt, Dr Ball, and Dr Mallbris own stock in and are employees of Eli Lilly and Company.


© 2018  Publié par Elsevier Masson SAS.
Ajouter à ma bibliothèque Retirer de ma bibliothèque Imprimer
Export

    Export citations

  • Fichier

  • Contenu

Vol 79 - N° 5

P. 824 - novembre 2018 Retour au numéro
Article précédent Article précédent
  • Granuloma annulare's triangular association with malignancy
  • Warren R. Heymann
| Article suivant Article suivant
  • Association between Breslow thickness and dermoscopic findings in acral melanoma
  • Je-Ho Mun, Gwanghyun Jo, Claudia C. Darmawan, Jin Park, Jung Min Bae, HyunJu Jin, Woo-Il Kim, Hoon-Soo Kim, Hyun-Chang Ko, Byung-Soo Kim, Moon-Bum Kim

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.