Rapid Improvements in Itch with Tapinarof Cream 1% Once Daily in Two Phase 3 Trials in Adults with Mild to Severe Plaque Psoriasis

被引:4
作者
Kircik, Leon [1 ]
Zirwas, Matthew [2 ]
Kwatra, Shawn G. [3 ]
Lewitt, G. Michael [4 ]
Glover, Holly [5 ]
Chao, Tomas [6 ]
Brown, Philip M. [7 ]
Rubenstein, David S. [7 ]
Tallman, Anna M. [7 ]
机构
[1] Icahn Sch Med Mt Sinai, 5 E 98th St,5th Fl, New York, NY 10029 USA
[2] DOCS Dermatol, 2359 Main St, Bexley, OH 43209 USA
[3] Johns Hopkins Univ, Sch Med, Baltimore, MD USA
[4] Illinois Dermatol Inst, Chicago, IL USA
[5] Metroplex Dermatol, Arlington, TX USA
[6] Atlanta North Dermatol, Woodstock, GA USA
[7] Dermavant Sci Inc, 3300 Paramount Pkwy,Suite 150, Morrisville, NC 27560 USA
关键词
Itch; Pruritus; Phase 3 PSOARING trials; Plaque psoriasis; Tapinarof cream 1% QD; Topical therapy; Aryl hydrocarbon receptor agonist; PRURITUS; PATIENT;
D O I
10.1007/s13555-023-01068-x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Introduction: Patients with psoriasis report pruritus as their most bothersome symptom. Tapinarof cream 1% once daily demonstrated significant efficacy versus vehicle and was well tolerated in adults with mild to severe plaque psoriasis in two 12-week trials: PSOARING 1 (NCT03956355) and PSOARING 2 (NCT03983980). Here, we present patient-reported pruritus outcomes from these trials.Methods: Outcomes included a Peak Pruritus Numerical Rating Scale (PP-NRS) score of 0 or 1 (itch-free state); Dermatology Life Quality Index (DLQI) itch item scores; and Psoriasis Symptom Diary (PSD) itch item scores.Results: Analyses included 683 tapinarof- and 342 vehicle-treated patients. At baseline, mean pruritus scores were similar across trials with only 7-11% of patients reporting an itch-free state. At week 12, the proportion of tapinarof-treated patients achieving an itch-free state was 50% in both trials compared with 32% (P = 0.0007) and 27% (P < 0.0001) in the vehicle groups. Improvements were apparent at the earliest assessments with continued improvement over the course of the trials. There were rapid and statistically significant improvements in the proportion of patients with a >= 4-point improvement in PP-NRS for tapinarof-treated patients versus vehicle from week 2 with 68% vs 46% (P = 0.0004) and 60% vs 31% (P = 0.0001) at week 12 achieving a response in each trial. Significantly greater reductions in itch with tapinarof versus vehicle were also demonstrated at week 12 for DLQI itch item 1 (P = 0.0026 and P < 0.0001), PSD item 1 (both P < 0.0001), and PSD item 2 (both P < 0.0001).Conclusion: Tapinarof was highly efficacious in reducing pruritus across multiple patient-reported outcome measures, with rapid, statistically significant, and clinically meaningful improvements. The high proportion of patients achieving the treatment target of an itch-free state at week 12 (50%) is a noteworthy clinical outcome for a non-steroidal topical cream in the treatment of mild to severe plaque psoriasis.
引用
收藏
页码:201 / 211
页数:11
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