Courtney Ashling, Adamson Sarah Rose, Veysey Emma
Vulvar Disorders and Dermatology Unit, The Royal Women's Hospital, Parkville, Victoria, Australia.
J Low Genit Tract Dis. 2025 Apr 1;29(2):190-194. doi: 10.1097/LGT.0000000000000862. Epub 2024 Dec 9.
This case series aims to evaluate the demographic features, disease characteristics, and treatment outcomes of 8 patients receiving subcutaneous (SC) adalimumab for severe, refractory vulval lichen sclerosus (VLS) and/or vulval lichen planus (VLP). Both conditions are chronic inflammatory dermatoses that significantly impair quality of life, and although first-line treatment typically involves potent to ultrapotent topical corticosteroids, managing severe cases is challenging due to a lack of FDA-approved systemic therapies. Adalimumab, a TNF-α inhibitor, may offer a promising alternative by targeting the inflammatory cytokine implicated in the pathogenesis of both conditions.
Eight patients received SC adalimumab for VLS and/or VLP at a tertiary referral vulvar disorders clinic from September 2020 to June 2024. Among the 8 patients, 4 had VLS/VLP clinical overlap, 2 had VLP, and 2 had VLS. Evaluation included patient-reported outcome measures (PROMs) namely the vulval life quality index (VLQI) and numerical rating scales for itch and pain, and objective clinical severity was assessed by a vulvar dermatologist based on cutaneous signs and architectural features.
Adalimumab was well tolerated by 6 of 8 patients who received treatment for at least 9 months. Varying degrees of clinical improvement were observed in cutaneous signs and PROMs, including significant reductions in vulval life quality index scores for 6 patients. Architectural changes remained stable throughout treatment for all patients.
This case series indicates that SC adalimumab may be a treatment option for patients with severe, refractory VLS and VLP, as demonstrated by significant improvements in PROMs. The observed clinical benefits suggest that adalimumab targets key inflammatory pathways in these conditions. Controlled trials are necessary to further validate these findings and define adalimumab's role in managing severe refractory VLS and VLP. Future research should also investigate long-term efficacy and safety, as well as potential predictors of treatment response, to optimize care for this challenging patient population.
本病例系列旨在评估8例接受皮下注射阿达木单抗治疗重度难治性外阴硬化性苔藓(VLS)和/或外阴扁平苔藓(VLP)患者的人口统计学特征、疾病特征及治疗结果。这两种疾病均为慢性炎症性皮肤病,会显著影响生活质量,虽然一线治疗通常包括强效至超强效外用糖皮质激素,但由于缺乏FDA批准的全身治疗方法,管理重症病例具有挑战性。阿达木单抗是一种肿瘤坏死因子-α(TNF-α)抑制剂,通过靶向这两种疾病发病机制中涉及的炎性细胞因子,可能提供一种有前景的替代治疗方法。
2020年9月至2024年6月,8例患者在一家三级转诊外阴疾病诊所接受皮下注射阿达木单抗治疗VLS和/或VLP。8例患者中,4例有VLS/VLP临床重叠,2例有VLP,2例有VLS。评估包括患者报告的结局指标(PROMs),即外阴生活质量指数(VLQI)以及瘙痒和疼痛的数字评分量表,外阴皮肤科医生根据皮肤体征和结构特征评估客观临床严重程度。
8例接受治疗至少9个月的患者中有6例对阿达木单抗耐受性良好。在皮肤体征和PROMs方面观察到不同程度的临床改善,包括6例患者的外阴生活质量指数评分显著降低。所有患者在整个治疗过程中结构变化保持稳定。
本病例系列表明,皮下注射阿达木单抗可能是重度难治性VLS和VLP患者的一种治疗选择,PROMs的显著改善证明了这一点。观察到的临床益处表明阿达木单抗靶向这些疾病的关键炎症途径。需要进行对照试验以进一步验证这些发现,并确定阿达木单抗在管理重度难治性VLS和VLP中的作用。未来的研究还应调查长期疗效和安全性,以及治疗反应的潜在预测因素,以优化对这一具有挑战性患者群体的护理。