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Sustained Improvements in Clinical and Patient-Reported Outcomes and Quality of Life Through 5 Years Among Ixekizumab-Treated Patients with Complete Clearance of Scalp Psoriasis by Week 60.
Egeberg, Alexander; Hawkes, Jason E; Somani, Najwa; Burge, Russel; See, Kyoungah; Gallo, Gaia; McKean-Matthews, Missy; Gooderham, Melinda; Han, George; Armstrong, April.
Afiliação
  • Egeberg A; Department of Dermatology, Bispebjerg Hospital, Copenhagen, Denmark. alexander.egeberg@gmail.com.
  • Hawkes JE; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark. alexander.egeberg@gmail.com.
  • Somani N; Integrative Skin Science and Research, Pacific Skin Institute University, Sacramento, CA, USA.
  • Burge R; Eli Lilly and Company, Indianapolis, IN, USA.
  • See K; Eli Lilly and Company, Indianapolis, IN, USA.
  • Gallo G; Department of Pharmaceutical Sciences, University of Cincinnati, Cincinnati, OH, USA.
  • McKean-Matthews M; Eli Lilly and Company, Indianapolis, IN, USA.
  • Gooderham M; Eli Lilly and Company, Indianapolis, IN, USA.
  • Han G; Syneos Health, Raleigh, NC, USA.
  • Armstrong A; SKiN Centre for Dermatology, Peterborough, ON, Canada.
Dermatol Ther (Heidelb) ; 14(4): 1007-1018, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38647975
ABSTRACT

INTRODUCTION:

Ixekizumab, a high-affinity monoclonal antibody that selectively targets interleukin-17A, is approved for the treatment of moderate-to-severe plaque psoriasis. Since scalp psoriasis can be burdensome and challenging to treat with non-systemic therapies, this post hoc analysis focused on scalp psoriasis in patients with moderate-to-severe plaque psoriasis and baseline scalp involvement. The analysis considered a holistic concept of clearance through 5 years of ixekizumab treatment.

METHODS:

Ixekizumab-treated patients with baseline scalp involvement were pooled from three multicenter, randomized, double-blind, placebo-controlled, phase 3 trials (integrated UNCOVER-1/2 and UNCOVER-3). Analyses were performed on a subpopulation of patients who achieved complete resolution of scalp psoriasis at Week 60 (i.e., Week 60 Psoriasis Scalp Severity Index [PSSI-0] responders) and on the overall patient population (i.e., Week 60 PSSI-0 responders and non-responders), which was used as a reference. Clinical outcomes (PSSI), patient-reported outcomes (Itch Numeric Rating Scale [NRS] score, Skin Pain Visual Analogue Scale [VAS]), quality of life (Dermatology Life Quality Index [DLQI]), and concurrent outcomes were assessed from baseline through 5 years. Descriptive statistics of observed data were reported.

RESULTS:

After 60 weeks of ixekizumab treatment, 88.4% (UNCOVER-1/2) and 75.9% (UNCOVER-3) of patients with baseline scalp involvement achieved complete clearance (PSSI-0) of scalp psoriasis. Substantial improvements in the clinical outcomes (PSSI), patient-reported outcomes (Itch NRS, Skin Pain VAS), and quality of life (DLQI) were achieved by Week 60 and sustained through Week 264 in the Week 60 PSSI-0 responders and in the overall patient population. Additionally, a significant proportion of Week 60 PSSI-0 responders achieved concurrent complete scalp and skin clearance and quality of life improvement through 5 years.

CONCLUSIONS:

Continued treatment with ixekizumab provided long-term sustained scalp clearance over 5 years to patients with moderate-to-severe plaque psoriasis and baseline scalp involvement, and holistic improvements occurred across clinical outcomes, patient-reported outcomes, and quality of life. CLINICAL TRIAL NUMBERS NCT01474512 (UNCOVER-1), NCT01597245 (UNCOVER-2), and NCT01646177 (UNCOVER-3).
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article