Department of Dermatology, Yale School of Medicine, New Haven, Connecticut.
Department of Dermatology, Lahey Hair Loss Center of Excellence, Lahey Hospital and Medical Center, Burlington, Massachusetts.
J Am Acad Dermatol. 2024 Nov;91(5):880-888. doi: 10.1016/j.jaad.2024.06.097. Epub 2024 Jul 23.
Alopecia areata (AA) is a hair loss disorder that can seriously impact quality of life. Janus kinase (JAK) inhibitors, including deuruxolitinib, have previously demonstrated significant hair regrowth in AA.
The Phase 3 THRIVE-AA1 randomized, double-blinded, placebo-controlled trial (NCT04518995) evaluated the safety and efficacy of the oral JAK1/JAK2 inhibitor deuruxolitinib in adult patients with AA.
Patients aged 18-65 years with ≥50% hair loss were randomized to deuruxolitinib 8 mg twice daily, deuruxolitinib 12 mg twice daily, or placebo for 24 weeks. The primary end point was the percentage of patients achieving a Severity of Alopecia Tool score ≤20. A key secondary end point was the percentage of satisfaction of hair patient-reported outcome responders.
Significantly higher proportions of patients taking deuruxolitinib met the primary end point (8 mg 29.6%; 12 mg 41.5% versus placebo 0.8%). Both deuruxolitinib doses achieved significant improvements in all secondary end points versus placebo, including satisfaction of hair patient-reported outcome (8 mg 42.1%; 12 mg 53.0% versus placebo 4.7%). Most treatment-emergent adverse events were mild or moderate, consistent with other oral JAK inhibitors.
Further studies are required to understand longer-term safety, efficacy, and impact of treatment cessation.
Both doses of deuruxolitinib were effective for hair regrowth. Patient satisfaction aligned with hair growth.
斑秃(AA)是一种脱发疾病,可严重影响生活质量。Janus 激酶(JAK)抑制剂,包括度鲁特韦,先前已证明在 AA 中有显著的毛发生长作用。
III 期 THRIVE-AA1 随机、双盲、安慰剂对照试验(NCT04518995)评估了口服 JAK1/JAK2 抑制剂度鲁特韦在成人 AA 患者中的安全性和疗效。
年龄在 18-65 岁之间、脱发≥50%的患者被随机分为度鲁特韦 8mg 每日两次、度鲁特韦 12mg 每日两次或安慰剂治疗 24 周。主要终点是达到严重度脱发评估工具评分≤20的患者比例。主要次要终点是毛发患者报告结局应答者满意度的比例。
服用度鲁特韦的患者比例显著更高,达到主要终点(8mg 29.6%;12mg 41.5%,安慰剂 0.8%)。与安慰剂相比,两种度鲁特韦剂量均在所有次要终点取得显著改善,包括毛发患者报告结局满意度(8mg 42.1%;12mg 53.0%,安慰剂 4.7%)。大多数治疗中出现的不良事件为轻度或中度,与其他口服 JAK 抑制剂一致。
需要进一步研究以了解长期安全性、疗效和治疗停止的影响。
两种剂量的度鲁特韦均对毛发生长有效。患者满意度与毛发生长一致。