Effectiveness and safety of liposomal rapamycin for the treatment of facial angiofibromas in tuberous sclerosis.

IF 1 Q4 PHARMACOLOGY & PHARMACY FARMACIA HOSPITALARIA Pub Date : 2024-06-07 DOI:10.1016/j.farma.2024.04.023
Clara Cortell-Fuster, María Amparo Martínez-Gómez, Ana Cristina Cercós-Lleti, Mónica Climente-Martí, Tania Díaz-Corpas, Almudena Mateu-Puchades, Ángeles Revert-Fernández
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Abstract

Aim: Topical rapamycin is the pharmacological treatment of choice for facial angiofibromas in rare tuberous sclerosis disease. A new, more advanced, and complex formula was developed in our pharmacy service: rapamycin 0.4% liposomal formulation, with better organoleptic characteristics and a more favorable release profile of the active ingredient. The purpose of this study is to evaluate the effectiveness and safety of liposomal topical rapamycin for the treatment of facial injuries in this rare disease.

Method: This was an observational, prospective, and multicenter study. Effectiveness was evaluated mainly through facial angiofibromas severity index (FASI), investigator's global assessment (IGA) scores, and dermatology life quality index (DLQI) questionnaire. To assess the safety profile of rapamycin, adverse reactions were reported, and blood tests and blood rapamycin levels were performed during treatment.

Results: Eleven patients were included, of which 8/11 (73%) patients obtained successful treatment according to FASI and IGA scores after 24 weeks of treatment. Statistical analysis demonstrated a significant improvement (p<.05) in FASI and IGA scores, erythema, and FA size after treatment with rapamycin liposomal formulation (FASI before treatment, median (interquartile range): 6.0 (2.0), FASI after treatment: 3.5 (2.0), p=.0063). Five patients also improved their quality of life after treatment. Regarding safety profile of rapamycin, the most common adverse reaction was mild pruritus and 2 patients reported erythema, who discontinued treatment prematurely. All hematological tests were normal, and blood rapamycin levels were undetectable.

Conclusions: After galenic improvements and clinical evaluations, the rapamycin liposomal formulation proved to be effective and safe for this therapeutic indication. This new formulation was included as a magistral formula in our hospital pharmacy service, now accessible for prescribing by dermatologists. Drug development in hospital pharmacy is often the only pharmacological alternative available to treat the symptoms of rare diseases, when treatment options are limited or inadequate.

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脂质体雷帕霉素治疗结节性硬化症面部血管纤维瘤的有效性和安全性。
目的:外用雷帕霉素是治疗罕见结节性硬化症面部血管纤维瘤的首选药物。我院药剂科开发了一种更先进、更复杂的新配方:雷帕霉素 0.4% 脂质体制剂,具有更好的感官特性和更有利的活性成分释放谱。本研究旨在评估脂质体外用雷帕霉素治疗这种罕见疾病面部损伤的有效性和安全性:这是一项观察性、前瞻性和多中心研究。主要通过面部血管纤维瘤严重程度指数(FASI)、研究者总体评估(IGA)评分和皮肤科生活质量指数(DLQI)问卷评估疗效。为了评估雷帕霉素的安全性,研究人员报告了不良反应,并在治疗期间进行了血液化验和血雷帕霉素水平检测:共纳入11名患者,其中8/11(73%)名患者在治疗24周后根据FASI和IGA评分获得成功治疗。统计分析表明,患者的病情有了明显改善(p结论:经过基因学改进和临床评估,雷帕霉素脂质体制剂被证明对这一治疗适应症有效且安全。我们的医院药房已将这种新制剂列为普通配方,皮肤科医生现在可以开具处方。在治疗方案有限或不足的情况下,医院药房的药物开发往往是治疗罕见疾病症状的唯一药物选择。
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来源期刊
FARMACIA HOSPITALARIA
FARMACIA HOSPITALARIA PHARMACOLOGY & PHARMACY-
CiteScore
1.90
自引率
21.40%
发文量
46
审稿时长
37 days
期刊介绍: Una gran revista para acceder a los mejores artículos originales y revisiones de la farmacoterapia actual. Además, es Órgano de expresión científica de la Sociedad Española de Farmacia Hospitalaria, y está indexada en Index Medicus/Medline, EMBASE/Excerpta Médica, Alert, Internacional Pharmaceutical Abstracts y SCOPUS.
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