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鲁索利替尼乳膏治疗特应性皮炎患者瘙痒迅速缓解。

Rapid pruritus reduction with ruxolitinib cream treatment in patients with atopic dermatitis.

机构信息

Oregon Medical Research Center, Portland, Oregon, USA.

Icahn School of Medicine at Mount Sinai, New York, New York, USA.

出版信息

J Eur Acad Dermatol Venereol. 2023 Jan;37(1):137-146. doi: 10.1111/jdv.18571. Epub 2022 Sep 21.

Abstract

BACKGROUND

Ruxolitinib cream is a topical formulation of ruxolitinib, a Janus kinase (JAK) 1/JAK2 inhibitor.

OBJECTIVES

To report timing and magnitude of effect of ruxolitinib cream on itch in patients with atopic dermatitis (AD), a highly pruritic inflammatory skin disease.

METHODS

Two phase 3 trials (TRuE-AD1 [NCT03745638]/TRuE-AD2 [NCT03745651]) enrolled patients aged ≥12 years with AD for ≥2 years, Investigator's Global Assessment score of 2 or 3, and 3%-20% affected body surface area. Patients (total N = 1249; median age, 32 years) were randomised (2:2:1) to twice daily 0.75% ruxolitinib cream, 1.5% ruxolitinib cream or vehicle cream for 8 weeks of double-blinded treatment. Worst itch was measured using the numerical rating scale (NRS).

RESULTS

Significantly more patients who applied ruxolitinib cream (either strength) achieved a ≥2-point itch reduction (NRS2) within approximately 12 h versus vehicle (0.75%/1.5% ruxolitinib cream, 16.3%/13.1%; vehicle, 6.9%; both P < 0.05), with further improvements through Week 8 (58.3%/65.1% vs 29.4%; both P < 0.0001). A ≥4-point itch reduction (NRS4) was achieved by significantly more patients who applied 0.75%/1.5% ruxolitinib cream versus vehicle by Day 2 (8.9%/11.2% vs 2.1%; P < 0.005); higher rates were observed at Week 8 (41.5%/51.5% vs 15.8%; P < 0.0001). Median time for the 0.75%/1.5% ruxolitinib cream groups to achieve NRS4 from baseline was 15.0/13.0 days; this endpoint was not reached by the vehicle group.

CONCLUSIONS

Ruxolitinib cream demonstrated rapid improvement in itch in patients with mild to moderate AD that was sustained for 8 weeks. Significantly more patients applying ruxolitinib cream achieved itch NRS2 within approximately 12 h and itch NRS4 by Day 2 versus vehicle.

摘要

背景

鲁索替尼乳膏是鲁索替尼的一种局部制剂,鲁索替尼是一种 Janus 激酶(JAK)1/JAK2 抑制剂。

目的

报告在特应性皮炎(AD)患者中,鲁索替尼乳膏对瘙痒的作用时间和强度,AD 是一种高度瘙痒的炎症性皮肤病。

方法

两项 3 期临床试验(TRuE-AD1[NCT03745638]/TRuE-AD2[NCT03745651])招募了年龄≥12 岁、AD 病史≥2 年、研究者整体评估(IGA)评分为 2 或 3 分且体表面积受累 3%-20%的患者。患者(共 1249 例;中位年龄 32 岁)被随机(2:2:1)分为每日两次 0.75%鲁索替尼乳膏、1.5%鲁索替尼乳膏或赋形剂乳膏组,进行 8 周的双盲治疗。使用数字评分量表(NRS)测量最严重瘙痒。

结果

与赋形剂相比,应用鲁索替尼乳膏(任一种浓度)的患者在大约 12 小时内达到瘙痒 NRS2 至少改善 2 分的比例显著更高(0.75%/1.5%鲁索替尼乳膏组为 16.3%/13.1%,赋形剂组为 6.9%;均 P<0.05),并且在第 8 周时进一步改善(58.3%/65.1%vs29.4%;均 P<0.0001)。应用 0.75%/1.5%鲁索替尼乳膏的患者在第 2 天达到瘙痒 NRS4(至少改善 4 分)的比例显著更高(8.9%/11.2%vs2.1%;P<0.005);在第 8 周时,该比例更高(41.5%/51.5%vs15.8%;P<0.0001)。0.75%/1.5%鲁索替尼乳膏组达到瘙痒 NRS4 的中位时间为 15.0/13.0 天,而赋形剂组未达到该终点。

结论

鲁索替尼乳膏治疗轻中度 AD 患者的瘙痒,疗效迅速,持续 8 周。与赋形剂相比,应用鲁索替尼乳膏的患者在大约 12 小时内达到瘙痒 NRS2 的比例显著更高,在第 2 天达到瘙痒 NRS4 的比例更高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0040/10087253/ef0e624da0f5/JDV-37-137-g006.jpg

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