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Long-term, durable, absolute Psoriasis Area and Severity Index and health-related quality of life improvements with risankizumab treatment: a post hoc integrated analysis of patients with moderate-to-severe plaque psoriasis.
Gooderham, M; Pinter, A; Ferris, L K; Warren, R B; Zhan, T; Zeng, J; Soliman, A M; Kaufmann, C; Kaplan, B; Photowala, H; Strober, B.
Affiliation
  • Gooderham M; SKiN Centre for Dermatology, Probity Medical Research and Queen's University, Peterborough, ON, Canada.
  • Pinter A; Department of Dermatology, University Hospital Frankfurt am Main, Frankfurt am Main, Germany.
  • Ferris LK; Department of Dermatology, University of Pittsburgh, Pittsburgh, PA, USA.
  • Warren RB; The Dermatology Centre, Salford Royal NHS Foundation Trust, Manchester NIHR Biomedical Research Centre, University of Manchester, Manchester, UK.
  • Zhan T; AbbVie, Inc., North Chicago, IL, USA.
  • Zeng J; AbbVie, Inc., North Chicago, IL, USA.
  • Soliman AM; AbbVie, Inc., North Chicago, IL, USA.
  • Kaufmann C; AbbVie, Inc., North Chicago, IL, USA.
  • Kaplan B; AbbVie, Inc., North Chicago, IL, USA.
  • Photowala H; AbbVie, Inc., North Chicago, IL, USA.
  • Strober B; Yale University, New Haven, CT and Central Connecticut Dermatology Research, Cromwell, CT, USA.
J Eur Acad Dermatol Venereol ; 36(6): 855-865, 2022 Jun.
Article in En | MEDLINE | ID: mdl-35174556
ABSTRACT

BACKGROUND:

Risankizumab has demonstrated durable, high rates of efficacy in patients with moderate-to-severe plaque psoriasis as assessed by the achievement of relative Psoriasis Area and Severity Index (PASI) improvement and Dermatology Life Quality Index (DLQI) 0/1.

OBJECTIVES:

The aim of this post hoc analysis is to assess the achievement of absolute PASI thresholds and related improvements in health-related quality of life (HRQoL) in patients with moderate-to-severe plaque psoriasis treated with (i) risankizumab compared with ustekinumab, and (ii) long-term (>52 weeks to 172 weeks) risankizumab.

METHODS:

Data from patients randomised to 150 mg risankizumab or 45 or 90 mg ustekinumab in replicate randomised controlled trials UltIMMa-1 and UltIMMa-2 were analysed for the achievement of absolute PASI thresholds PASI ≤ 3, PASI ≤ 1, and PASI = 0, time to achieve these thresholds, and combined PASI and DLQI endpoints. Data from pat ients initially randomised to risankizumab who continued on risankizumab in the open-label extension study LIMMitless were analysed for the achievement of absolute PASI levels, mean DLQI scores, and DLQI 0/1.

RESULTS:

Significantly greater proportions of patients treated with risankizumab compared with ustekinumab achieved PASI ≤ 3, PASI ≤ 1, and PASI = 0, as well as combined endpoints for absolute PASI and DLQI [(PASI ≤ 3 and DLQI ≤ 5) or (PASI ≤ 1 and DLQI 0/1)]. The median time to first achieve PASI ≤ 3, PASI ≤ 1, and PASI = 0 was significantly lower for risankizumab-treated patients compared with ustekinumab-treated patients. Among patients treated with long-term risankizumab, more than 90% achieved PASI ≤ 3 though week 172 and more than 80% achieved DLQI 0/1. Low absolute PASI scores corresponded with low mean absolute DLQI scores through week 172 of continuous risankizumab treatment.

CONCLUSIONS:

Risankizumab treatment demonstrated high rates of rapid and durable efficacy as measured by absolute PASI thresholds and improvements in patient HRQoL.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psoriasis / Ustekinumab Type of study: Clinical_trials Aspects: Patient_preference Limits: Humans Language: En Journal: J Eur Acad Dermatol Venereol Journal subject: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Year: 2022 Document type: Article Affiliation country: Canadá

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Psoriasis / Ustekinumab Type of study: Clinical_trials Aspects: Patient_preference Limits: Humans Language: En Journal: J Eur Acad Dermatol Venereol Journal subject: DERMATOLOGIA / DOENCAS SEXUALMENTE TRANSMISSIVEIS Year: 2022 Document type: Article Affiliation country: Canadá
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