Low-Dose Baricitinib Plus Narrow-Band Ultraviolet B for the Treatment of Progressive Non-Segmental Vitiligo: A Prospective, Controlled, Open-Label Study.

IF 3.9 3区 医学 Q2 CELL BIOLOGY Pigment Cell & Melanoma Research Pub Date : 2024-10-23 DOI:10.1111/pcmr.13209
Zhonghui Hu, Lu Lu, Jindi Feng, Hongbin Song, Shiyu Zhang, Lu Yang, Yuehua Liu, Tao Wang
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Abstract

Vitiligo is a chronic autoimmune disease, and current treatments for vitiligo have limited efficacy. Janus kinase (JAK) inhibitors could offer new therapeutic options. To evaluate the efficacy and safety of baricitinib, an oral JAK1/2 inhibitor, combined with narrow-band ultraviolet B (NB-UVB) in vitiligo treatment. This prospective, controlled, open-label study included adults with progressive non-segmental vitiligo (NSV). Patients were assigned to combination therapy with baricitinib 2 mg daily and NB-UVB three times a week or NB-UVB alone three times a week (control). The primary endpoint was the proportion of patients achieving 50% or greater improvement from baseline in the total Vitiligo Area Scoring Index (T-VASI50) at week 16. Of the 33 patients (mean age, 34.1 years; 27.3% women) who completed the study, 12 of 17 (70.6%) patients in the combination group and 2 of 16 (12.5%) in the control group had a T-VASI50 response at week 16 (relative risk [RR] = 5.6; 95% CI = 1.5-21.4; p = 0.001). Adverse events were minor, including erythema, mild blister after phototherapy and acne. Combination therapy with low-dose baricitinib and NB-UVB was effective and well tolerated in adults with progressive NSV.

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低剂量巴利替尼加窄带紫外线 B 治疗进展期非节段性白癜风:一项前瞻性、对照、开放标签研究。
白癜风是一种慢性自身免疫性疾病,目前治疗白癜风的方法疗效有限。Janus激酶(JAK)抑制剂可提供新的治疗选择。目的是评估口服JAK1/2抑制剂巴利昔尼(baricitinib)联合窄带紫外线B(NB-UVB)治疗白癜风的疗效和安全性。这项前瞻性、对照、开放标签研究纳入了进展期非节段性白癜风(NSV)成人患者。患者被分配接受巴利昔尼(baricitinib)每天2毫克、NB-UVB每周三次的联合治疗,或仅接受NB-UVB每周三次的治疗(对照组)。主要终点是在第16周时,白癜风总面积评分指数(T-VASI50)比基线提高50%或以上的患者比例。在完成研究的 33 名患者(平均年龄 34.1 岁;27.3% 为女性)中,联合用药组 17 名患者中有 12 名(70.6%)在第 16 周时对 T-VASI50 有反应,对照组 16 名患者中有 2 名(12.5%)(相对风险 [RR] = 5.6;95% CI = 1.5-21.4;P = 0.001)。不良反应较轻,包括红斑、光疗后轻度水疱和痤疮。小剂量巴利昔尼和NB-UVB联合疗法对进展期NSV成人患者有效且耐受性良好。
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来源期刊
Pigment Cell & Melanoma Research
Pigment Cell & Melanoma Research 医学-皮肤病学
CiteScore
8.90
自引率
2.30%
发文量
54
审稿时长
6-12 weeks
期刊介绍: Pigment Cell & Melanoma Researchpublishes manuscripts on all aspects of pigment cells including development, cell and molecular biology, genetics, diseases of pigment cells including melanoma. Papers that provide insights into the causes and progression of melanoma including the process of metastasis and invasion, proliferation, senescence, apoptosis or gene regulation are especially welcome, as are papers that use the melanocyte system to answer questions of general biological relevance. Papers that are purely descriptive or make only minor advances to our knowledge of pigment cells or melanoma in particular are not suitable for this journal. Keywords Pigment Cell & Melanoma Research, cell biology, melatonin, biochemistry, chemistry, comparative biology, dermatology, developmental biology, genetics, hormones, intracellular signalling, melanoma, molecular biology, ocular and extracutaneous melanin, pharmacology, photobiology, physics, pigmentary disorders
期刊最新文献
The Lipid Droplet Protein DHRS3 Is a Regulator of Melanoma Cell State. UVA Irradiation Promotes Melanoma Cell Proliferation Mediated by OPN3 Independently of ROS Production. Issue Information Bay 11-7082, an NF-κB Inhibitor, Prevents Post-Inflammatory Hyperpigmentation Through Inhibition of Inflammation and Melanogenesis. Low-Dose Baricitinib Plus Narrow-Band Ultraviolet B for the Treatment of Progressive Non-Segmental Vitiligo: A Prospective, Controlled, Open-Label Study.
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