State Key Laboratory of Oral Diseases, National Clinical Research Center for Oral Diseases, Department of Oral Medicine, West China Hospital of Stomatology, Sichuan University, Chengdu, China.
Department of Oral Mucosa, Shanghai Stomatological Hospital, Fudan University, Shanghai, China.
J Oral Pathol Med. 2021 Feb;50(2):251-259. doi: 10.1111/jop.13142. Epub 2020 Dec 23.
Tacrolimus has been used to treat various inflammatory skin diseases, but its safety for topical application on the oral mucosa is unknown. Exfoliative cheilitis (EC) is a chronic inflammatory disorder of the lips characterised by repeated scaling; it is difficult to manage. The aim of this study was to assess the efficacy and safety of tacrolimus 0.03% ointment as a topical treatment in patients with EC.
In this randomised controlled clinical trial, 40 patients with EC were randomly assigned to receive either tacrolimus 0.03% ointment (experimental group, n = 20) or triamcinolone acetonide 0.1% cream (control group, n = 20) treatment for a 3-week period. Medication was administered in 3, 2 and 1 daily doses during the first, second and third weeks, respectively. The patients with complete healing were followed up for 3 months. The clinical outcomes were measured, including the scores regarding signs (scale, dryness, rhagades and swelling) and symptoms (rough, dry, pain, pruritus and burning sensation) at every visit. Blood concentrations of tacrolimus were assessed.
After the 3-week treatment, healing rates of scale in the experimental and control groups were 65% and 10%, respectively (P = .018). Improvement in all signs and two symptoms (rough, pruritus) was much greater in the experimental group (P < .05). The 3-month recurrence rate was higher in the control group (P = .029). Tacrolimus blood concentrations were in the safe range (< 5 ng/mL).
Topical tacrolimus 0.03% ointment has good short-term efficacy and safety for treating EC.
他克莫司已被用于治疗各种炎症性皮肤病,但局部应用于口腔黏膜的安全性尚不清楚。剥脱性唇炎(EC)是一种以唇部反复脱屑为特征的慢性炎症性疾病,难以治疗。本研究旨在评估他克莫司 0.03%软膏作为 EC 患者局部治疗的疗效和安全性。
在这项随机对照临床试验中,40 名 EC 患者被随机分为他克莫司 0.03%软膏(实验组,n=20)或曲安奈德 0.1%乳膏(对照组,n=20)治疗组,治疗期为 3 周。在第 1、2 和第 3 周,分别每天给予 3、2 和 1 次剂量的药物。完全治愈的患者随访 3 个月。测量临床结果,包括每次就诊时的体征(鳞屑、干燥、皲裂和肿胀)和症状(粗糙、干燥、疼痛、瘙痒和烧灼感)评分。评估他克莫司的血药浓度。
治疗 3 周后,实验组和对照组的鳞屑愈合率分别为 65%和 10%(P=0.018)。实验组所有体征和两个症状(粗糙、瘙痒)均有较大改善(P<0.05)。对照组的 3 个月复发率较高(P=0.029)。他克莫司的血药浓度在安全范围内(<5ng/mL)。
他克莫司 0.03%软膏治疗 EC 具有良好的短期疗效和安全性。