Chinese Journal of Dermatology ›› 2025, Vol. 58 ›› Issue (9): 856-859.doi: 10.35541/cjd.20240500

• Clinical experience • Previous Articles     Next Articles

Efficacy of baricitinib combined with ruxolitinib cream in the treatment of six patients with progressive nonsegmental vitiligo: a clinical observation

Zhu Tingting1,2, Li Weiran2, Pan Zhaobing3, Liu Hao4, Tang Xianfa2, Zhu Caihong2, Huang Hequn2, Duan Dawei2, Zhang Ruochen5, Chen Xiaojian5, Wang Yang2, Xue Qian2, Zhang Jurui1,Yang Lijing1,Zhang Xuejun1,2, Huang He1,2, Zhang Bo1,2   

  1. 1Dermatology Center, Boao Super Hospital, Qionghai 571437, Hainan, China; 2Department of Dermatology and Venereology, the First Affiliated Hospital, Institute of Dermatology, Anhui Medical University, Hefei 230022, China; 3Hainan Provincial Dermatology Hospital, Haikou 570100, China; 4Department of Dermatology, the Second Affiliated Hospital of Hainan Medical University, Haikou 570311, China; 5Department of Dermatology, the Fourth Affiliated Hospital of Soochow University, Suzhou 215000, Jiangsu, China
  • Received:2024-09-19 Revised:2025-06-18 Online:2025-09-15 Published:2025-09-01
  • Contact: Zhang Bo E-mail:alvinbo@163.com
  • Supported by:
    Open Fund Project of Key Laboratory of Dermatology, Ministry of Education(AYFYS2024-5)

Abstract: 【Abstract】 Objective To evaluate the efficacy and safety of baricitinib combined with ruxolitinib cream in the treatment of progressive nonsegmental vitiligo. Methods Clinical data were retrospectively collected from patients with progressive nonsegmental vitiligo in Boao Super Hospital. All the patients were treated with oral baricitinib daily (2 mg/day for patients weighing ≤ 50 kg; 4 mg/day for those > 50 kg) in combination with topical application of ruxolitinib cream twice daily for 24 consecutive weeks. Disease severity was assessed using the facial vitiligo area scoring index (F-VASI) and total body VASI (T-VASI) at baseline, week 12, and week 24. Adverse reactions were monitored throughout the treatment course. Results Six patients with progressive nonsegmental vitiligo were collected, including 3 males and 3 females, aged 26 - 42 years, with the disease duration ranging from 0.5 to 25 years. At week 12, 3 patients achieved a 50% ~ < 75% improvement in facial vitiligo lesions (F-VASI 50), 1 patient achieved F-VASI 75 (75% ~ < 90% improvement), and 1 patient achieved T-VASI 50; at week 24, 4 patients achieved F-VASI 50, 1 patient achieved F-VASI 75, 1 patient achieved F-VASI 90 (≥ 90% improvement), and 3 patients achieved T-VASI 50. During the treatment, upper respiratory infection occurred in 1 patient, acne in 1 patient, pruritus in 2 patients, elevation of total cholesterol levels in 2 patients, and increase of high-density lipoprotein levels in 2 patients. No severe adverse events were observed during the treatment. Conclusion The combination therapy with baricitinib and ruxolitinib cream may have potential efficacy and safety in the treatment of progressive nonsegmental vitiligo.

Key words: Vitiligo, Janus kinase inhibitors, Baricitinib, Ruxolitinib, Treatment outcome, Efficacy, Safety