Secukinumab demonstrates superiority over narrow‐band ultraviolet B phototherapy in new‐onset moderate to severe plaque psoriasis patients: Week 52 results from the STEPIn study

Author:

Iversen Lars1,Conrad Curdin2ORCID,Eidsmo Liv345,Costanzo Antonio67ORCID,Narbutt Joanna8,Pinter Andreas9ORCID,Kingo Külli10,Rivera Diaz Raquel11ORCID,Kolbinger Frank12,Nanna ManikPrabhu13,Frueh Jennifer Annika13,Jagiello Piotr13

Affiliation:

1. Department of Dermatology and Venereology Aarhus University Hospital Aarhus Denmark

2. Department of Dermatology CHUV University Hospital and University of Lausanne (UNIL) Lausanne Switzerland

3. Department of Medicine Solna Karolinska Institutet Stockholm Sweden

4. Unit of Rheumatology Karolinska University Hospital Stockholm Sweden

5. Leo Foundation Skin Immunology Research Center University of Copenhagen Copenhagen Denmark

6. Department of Biomedical Sciences Humanitas University Milan Italy

7. Dermatology Unit IRCCS Humanitas Research Hospital Rozzano Italy

8. Dermoklinika Medical Centre Lodz Poland

9. Department of Dermatology, Venereology and Allergology Goethe‐Universität Frankfurt am Main Frankfurt Germany

10. Department of Dermatology University of Tartu, Dermatology Clinic, Tartu University Hospital Tartu Estonia

11. Department of Dermatology Hospital Universitario 12 de Octubre Madrid Spain

12. Department of Autoimmunity, Transplantation & Immunology Novartis Institutes for Biomedical Research Basel Switzerland

13. Novartis IMI AG Basel Switzerland

Abstract

AbstractBackgroundBiologic treatments have been studied mainly in patients with a long‐term history of psoriasis and previous treatment failures.ObjectivesThe purpose of this primary analysis of the STEPIn study is to determine whether early intervention with secukinumab in patients with new‐onset moderate to severe plaque psoriasis is superior to standard of care treatment with narrow band ultraviolet B (nb‐UVB) phototherapy.MethodsThe STEPIn study is a randomized, open‐label, multicentre study to investigate early intervention with 52 weeks of secukinumab 300 mg administered subcutaneously versus standard treatment with nb‐UVB phototherapy in patients with new‐onset (≤12 months) moderate to severe plaque psoriasis (NCT03020199). The primary and additional secondary endpoints were ≥90% improvement in Psoriasis Area and Severity Index (PASI 90) at Week 52 and Investigator's Global Assessment (IGA mod 2011) 0/1 response at Week 52, respectively.ResultsIn the secukinumab and nb‐UVB study arms, 77/80 and 76/80 randomized patients received at least one dose of study treatment, respectively. The primary endpoint was achieved: 91.1% (70/77) of patients achieved a PASI 90 response at Week 52 in the secukinumab arm versus 42.3% (32/76) in the nb‐UVB arm (p < 0.0001, odds ratio [OR] estimate [95% confidence intervals, CI] = 16.3 [5.6, 46.9]). The additional secondary endpoint was also achieved: 85.7% of patients achieved an IGA 0/1 response at Week 52 in the secukinumab arm versus 36.8% in the nb‐UVB arm (p < 0.0001). The safety data were consistent with the safety profiles of secukinumab and nb‐UVB with no new or unexpected safety signals.ConclusionsSecukinumab was superior to nb‐UVB in treating patients with new‐onset moderate to severe plaque psoriasis. The high and sustained skin clearance observed indicates that biologic treatment for psoriasis may be more effective if used early in the disease course.

Funder

Novartis Pharma

Publisher

Wiley

Subject

Infectious Diseases,Dermatology

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