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A head-to-head comparison of ixekizumab vs. guselkumab in patients with moderate-to-severe plaque psoriasis: 24-week efficacy and safety results from a randomized, double-blinded trial.
Blauvelt, A; Leonardi, C; Elewski, B; Crowley, J J; Guenther, L C; Gooderham, M; Langley, R G; Vender, R; Pinter, A; Griffiths, C E M; Tada, Y; Elmaraghy, H; Lima, R G; Gallo, G; Renda, L; Burge, R; Park, S Y; Zhu, B; Papp, K.
Afiliación
  • Blauvelt A; Oregon Medical Research Center, Portland, OR, USA.
  • Leonardi C; Central Dermatology, St Louis, MO, USA.
  • Elewski B; Deparment of Dermatology, University of Alabama, Birmingham, AL, USA.
  • Crowley JJ; Bakersfield Dermatology and Skin Cancer Medical Group, Bakersfield, CA, USA.
  • Guenther LC; Guenther Research Inc, London, ON, Canada.
  • Gooderham M; SKiN Centre for Dermatology, Peterborough, ON, Canada.
  • Langley RG; Dalhousie University, Halifax, NS, Canada.
  • Vender R; Dermatrials Research Inc, Hamilton, ON, Canada.
  • Pinter A; Clinic for Dermatology, Venereology and Allergology, University Hospital Frankfurt, Frankfurt am Main, Germany.
  • Griffiths CEM; Dermatology Centre, Salford Royal Hospital, NIHR Manchester Biomedical Research Centre, University of Manchester, Manchester, UK.
  • Tada Y; Department of Dermatology, Teikyo University School of Medicine, Tokyo, Japan.
  • Elmaraghy H; Eli Lilly and Company, Indianapolis, IN, USA.
  • Lima RG; Eli Lilly and Company, Indianapolis, IN, USA.
  • Gallo G; Eli Lilly and Company, Indianapolis, IN, USA.
  • Renda L; Eli Lilly and Company, Indianapolis, IN, USA.
  • Burge R; Eli Lilly and Company, Indianapolis, IN, USA.
  • Park SY; Eli Lilly and Company, Indianapolis, IN, USA.
  • Zhu B; Eli Lilly and Company, Indianapolis, IN, USA.
  • Papp K; Probity Medical Research, Inc., Waterloo, ON, Canada.
Br J Dermatol ; 184(6): 1047-1058, 2021 06.
Article en En | MEDLINE | ID: mdl-32880909
ABSTRACT

BACKGROUND:

Significantly more patients with moderate-to-severe plaque psoriasis treated with the interleukin (IL)-17A inhibitor ixekizumab vs. the IL-23p19 inhibitor guselkumab in the IXORA-R head-to-head trial achieved 100% improvement in Psoriasis Area and Severity Index (PASI 100) at week 12.

OBJECTIVES:

To compare skin and nail clearance and patient-reported outcomes for ixekizumab vs. guselkumab, up to week 24.

METHODS:

IXORA-R enrolled adults with moderate-to-severe plaque psoriasis, defined as static Physician's Global Assessment ≥ 3, PASI ≥ 12 and involved body surface area ≥ 10%. Statistical comparisons were performed using the Cochran-Mantel-Haenszel test stratified by pooled site. Time-to-first-event comparisons were performed using Kaplan-Meier analysis, and P-values were generated using adjusted log-rank tests stratified by treatment group. Cumulative days at clinical and patient-reported responses were compared by ancova. The trial was registered with ClinicalTrials.gov (NCT03573323).

RESULTS:

Of the 1027 patients randomly assigned, 90% completed the trial (465 of 520 ixekizumab and 459 of 507 guselkumab). As early as week 2 and through week 16, more patients on ixekizumab achieved PASI 100 (P < 0·01). At week 24, ixekizumab was noninferior to guselkumab (50% vs. 52%, difference -2·3%), with no statistically significant difference in PASI 100 (P = 0·41). More patients receiving ixekizumab showed completely clear nails at week 24 (52% vs. 31%, P = 0·007). The median time to first PASI 50/75/90 and PASI 100 were 2 and 7·5 weeks shorter, respectively, for patients on ixekizumab vs. guselkumab (P < 0·001). Patients on ixekizumab also had a greater cumulative benefit, with more days at PASI 90 and 100, with Dermatology Life Quality Index of 0 or 1, and itch free (P < 0·05). The frequency of serious adverse events was 3% for each group, with no new safety signals.

CONCLUSIONS:

Ixekizumab was noninferior to guselkumab in complete skin clearance and superior in clearing nails at week 24. Ixekizumab cleared skin more rapidly in patients with moderate-to-severe plaque psoriasis, with a greater cumulative benefit, than guselkumab. Overall, the safety findings were consistent with the known safety profile for ixekizumab.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Psoriasis Tipo de estudio: Clinical_trials Límite: Adult / Humans Idioma: En Revista: Br J Dermatol Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Psoriasis Tipo de estudio: Clinical_trials Límite: Adult / Humans Idioma: En Revista: Br J Dermatol Año: 2021 Tipo del documento: Article País de afiliación: Estados Unidos