Oregon Medical Research Center, Portland, Oregon, USA.
Icahn School of Medicine at Mount Sinai, New York, New York, USA.
J Eur Acad Dermatol Venereol. 2023 Jan;37(1):137-146. doi: 10.1111/jdv.18571. Epub 2022 Sep 21.
Ruxolitinib cream is a topical formulation of ruxolitinib, a Janus kinase (JAK) 1/JAK2 inhibitor.
To report timing and magnitude of effect of ruxolitinib cream on itch in patients with atopic dermatitis (AD), a highly pruritic inflammatory skin disease.
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).
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.
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.
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。
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。
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。
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。
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。