Boero Veronica, Caia Carlotta, Cetera Giulia E, Pesce Elisa, Uccello Serena, Villa Stefania, Montemurro Tiziana, Mykhailova Larysa, Merli Camilla E M, Monti Ermelinda, Filippi Flavia, Vercellini Paolo, Prati Daniele
Gynecology Unit, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Academic Center for Research on Adenomyosis and Endometriosis, Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Milan, Italy.
Blood Transfus. 2025 Jul-Aug;23(4):348-356. doi: 10.2450/BloodTransfus.875. Epub 2024 Dec 17.
Although topical corticosteroids (TCS) represent first-line treatment for vulvar lichen sclerosus (VLS) and as such should be prescribed to all women at time of diagnosis, approximately 30% of patients do not experience complete symptom resolution following such treatment. TCS may not effectively improve vulvar trophism and elasticity, both of which are crucial for sexual function. Owing to its regenerative and healing properties, cord blood platelet-rich plasma (CB-PRP) may represent an efficacious supplementary therapy, to be administered following first line treatment with TCS. The primary aim of this study was to assess safety and tolerability of CB-PRP in women with VLS.
This is a pilot study which precedes a randomized controlled trial of CB-PRP vs placebo in women with VLS. Ten consecutive patients with VLS, who had previously undergone standard TCS-treatment, received three vulvar CB-PRP injections monthly. Follow-up was conducted three months after the last injection using vulvoscopy and validated questionnaires to evaluate safety and tolerability, as well as patient satisfaction, symptom improvement, sexual function, psychological well-being, quality of life, frequency of TCS application as a maintenance treatment, vulvar trophism and architectural modifications.
No adverse clinical effects were observed. Five patients (50%) were either satisfied or very satisfied with the procedure, four (40%) were uncertain about their satisfaction with the treatment. One patient (10%) dropped out for personal reasons and was classified as unsatisfied according to an intention-to-treat analysis. At follow-up median numeric rating scale scores were significantly reduced for vulvar burning compared to baseline (p<0.05) there was a trend toward improvement in itching, dyspareunia, and dysuria. A significant improvement in sexual arousal and satisfaction was observed in all treated women (p<0.05).
CB-PRP may be a promising treatment for VLS. It appears to be safe and improve symptoms and sexual function.
尽管外用糖皮质激素(TCS)是外阴硬化性苔藓(VLS)的一线治疗方法,因此应在诊断时就给所有女性患者开此药,但约30%的患者在接受此类治疗后症状并未完全缓解。TCS可能无法有效改善外阴营养状况和弹性,而这两者对性功能都至关重要。由于脐带血富含血小板血浆(CB-PRP)具有再生和愈合特性,它可能是一种有效的辅助治疗方法,可在TCS一线治疗后使用。本研究的主要目的是评估CB-PRP在VLS女性患者中的安全性和耐受性。
这是一项先导研究,先于一项针对VLS女性患者的CB-PRP与安慰剂对比的随机对照试验。连续10例曾接受标准TCS治疗的VLS患者每月接受三次外阴CB-PRP注射。在最后一次注射三个月后进行随访,通过外阴镜检查和经过验证的问卷来评估安全性和耐受性,以及患者满意度、症状改善情况、性功能、心理健康、生活质量、作为维持治疗的TCS应用频率、外阴营养状况和结构改变。
未观察到不良临床效应。5例患者(50%)对该治疗过程感到满意或非常满意,4例(40%)对治疗满意度不确定。1例患者(10%)因个人原因退出,根据意向性分析被归类为不满意。随访时,与基线相比,外阴灼痛的数字评分量表中位数得分显著降低(p<0.05),瘙痒、性交困难和排尿困难有改善趋势。所有接受治疗的女性在性唤起和满意度方面均有显著改善(p<0.05)。
CB-PRP可能是一种有前景的VLS治疗方法。它似乎安全且能改善症状和性功能。