Efficacy of Apremilast in Patients with Psoriasis with Limited Skin Involvement, Including High-Impact Site Involvement: A Pooled Analysis of Six Trials - Report - MDSpire
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Effectiveness of Apremilast in Individuals with Psoriasis Exhibiting Minimal Skin Involvement and High-Impact Area Affected: A Combined Analysis of Six Clinical Trials
Clinical Report: Effectiveness of Apremilast in Psoriasis with Minimal Involvement
Overview
This pooled analysis of six clinical trials demonstrates that apremilast significantly improves skin clearance and quality of life in patients with plaque psoriasis exhibiting minimal skin involvement (3-10% BSA), particularly in high-impact anatomical sites.
Background
Plaque psoriasis can severely affect quality of life, even with limited skin involvement. High-impact sites, such as the scalp and genital area, are particularly burdensome, yet systemic treatment options for these patients are limited. The 2020 International Psoriasis Council guidelines recommend systemic therapy for those with high-impact site involvement.
Data Highlights
Week
Outcome
Percentage
16
BSA ≤ 1%
Not specified
16
BSA ≤ 3%
Not specified
16
BSA-75
Not specified
16
PASI < 3
Not specified
16
sPGA 0/1
Not specified
Key Findings
Apremilast improved skin clearance in patients with 3-10% BSA involvement.
Quality of life enhancements were noted at both weeks 16 and 32.
Benefits were sustained through week 32 for patients with high-impact site involvement.
Clinical trials included ADVANCE, DISCREET, STYLE, EMBRACE, UNVEIL, and PROMINENT.
Clinical Implications
Clinicians should consider apremilast for patients with limited plaque psoriasis, especially those affected in high-impact areas.
Conclusion
The findings support the use of apremilast as an effective treatment for patients with plaque psoriasis and limited skin involvement, particularly in high-impact areas.
by Bruce Strober, Mark Lebwohl, Peter van de Kerkhof, Linda Stein Gold, Joseph F. Merola, Yukari Okubo, Paolo Gisondi, Zhenwei Zhou, Siddharth Chaudhari, Cynthia Deignan, Ulrich Mrowietz
The expanded indication is supported by pharmacokinetic, safety, tolerability, exploratory efficacy, and long-term safety data from studies in children aged 2 to 5 years.