Abstract
ABSTRACT
Background
Traditional first‐line topical treatments for plaque psoriasis, particularly corticosteroids and vitamin D analogs, frequently have only limited efficacy for long‐term use, and present difficulties with safety and adherence.
Objectives
In this systematic review and meta‐analysis of randomized controlled trials (RCTs), we assessed the efficacy and safety of topical roflumilast 0.3% in patients with plaque psoriasis.
Methods
We searched the Cochrane CENTRAL, Embase, ClinicalTrials.gov, and PubMed databases from inception to May 2025 to identify relevant randomized clinical trials. Examined outcomes included Investigator's Global Assessment (IGA) or body‐IGA success (defined as clear or almost clear skin with at least a two‐grade improvement from baseline), scalp‐IGA (S‐IGA), intertriginous‐IGA (clear or almost clear status on the intertriginous‐IGA plus an at least 2‐grade improvement from baseline), Psoriasis Area and Severity Index (PASI)‐50, PASI‐75, PASI‐90, and PSSI‐75 (Psoriasis Scalp Severity Index 75%). Worst Itch‐Numeric Rating Scale (WI‐NRS) success, Psoriasis Symptoms Diary (PSD) score at 8 weeks, and adverse events (AEs) were also assessed. Statistical analysis was performed using Review Manager, while heterogeneity was quantified using the Higgins I² index.
Results
Analysis of five RCTs (1835 patients) showed topical roflumilast 0.3% improved IGA/body‐IGA (RR: 4.19; 95% CI: 2.49–7.04;
p
p
= 0.002), and I‐IGA (RR: 3.32; 95% CI: 2.11–5.22;
p
p
p
= 0.004).
Conclusions
These findings demonstrate that topical roflumilast 0.3% outperformed vehicle in efficacy and safety profile, underscoring its therapeutic potential in plaque psoriasis management.
Trial Registration:
PROSPERO ID: CRD420251064686.