[Artículo traducido] Efectividad y seguridad de sirólimus liposomal para el tratamiento de los angiofibromas faciales en la esclerosis tuberosa

IF 1.3 Q4 PHARMACOLOGY & PHARMACY FARMACIA HOSPITALARIA Pub Date : 2025-03-01 DOI:10.1016/j.farma.2024.08.005
Clara Cortell-Fuster , María Amparo Martínez-Gómez , Ana Cristina Cercós-Lleti , Mónica Climente-Martí , Tania Díaz-Corpas , Almudena Mateu-Puchades , Ángeles Revert-Fernández
{"title":"[Artículo traducido] Efectividad y seguridad de sirólimus liposomal para el tratamiento de los angiofibromas faciales en la esclerosis tuberosa","authors":"Clara Cortell-Fuster ,&nbsp;María Amparo Martínez-Gómez ,&nbsp;Ana Cristina Cercós-Lleti ,&nbsp;Mónica Climente-Martí ,&nbsp;Tania Díaz-Corpas ,&nbsp;Almudena Mateu-Puchades ,&nbsp;Ángeles Revert-Fernández","doi":"10.1016/j.farma.2024.08.005","DOIUrl":null,"url":null,"abstract":"<div><h3>Objective</h3><div>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.</div><div>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.</div></div><div><h3>Method</h3><div>This was an observational, prospective, and multicenter study. Effectiveness was evaluated mainly through Facial Angiofibroma 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.</div></div><div><h3>Results</h3><div>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 &lt; 0.05) 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], <em>p</em> = 0.0063). Five patients also improved their quality of life after treatment. Regarding safety profile of rapamycin, the most common adverse reaction was mild pruritus and two patients reported erythema, who discontinued treatment prematurely. All hematological tests were normal, and blood rapamycin levels were undetectable.</div></div><div><h3>Conclusions</h3><div>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.</div></div>","PeriodicalId":45860,"journal":{"name":"FARMACIA HOSPITALARIA","volume":"49 2","pages":"Pages T79-T85"},"PeriodicalIF":1.3000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"FARMACIA HOSPITALARIA","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1130634324001405","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Objective

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 Angiofibroma 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 < 0.05) 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 = 0.0063). Five patients also improved their quality of life after treatment. Regarding safety profile of rapamycin, the most common adverse reaction was mild pruritus and two 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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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:雷帕霉素是治疗罕见结节性硬化症并发面部血管纤维瘤的首选药物。我们的药学部门开发了一种新的、更先进的、更复杂的配方:雷帕霉素0.4%脂质体配方,具有更好的感官特性和更有利的活性成分释放谱。本研究的目的是评估脂质体外用雷帕霉素治疗面部损伤这种罕见疾病的有效性和安全性。方法:这是一项观察性、前瞻性、多中心研究。主要通过面部血管纤维瘤严重程度指数(FASI)、研究者整体评估(IGA)评分和皮肤病生活质量指数(DLQI)问卷对疗效进行评价。为了评估雷帕霉素的安全性,报告了不良反应,并在治疗期间进行了血液检查和血液雷帕霉素水平。结果:纳入11例患者,其中8/11(73%)患者在治疗24 周后,根据FASI和IGA评分获得成功治疗。结论:经galenic改善和临床评价,雷帕霉素脂质体制剂对该治疗指征是有效和安全的。这个新配方被包括在我们医院药房服务的一个地方公式,现在可为皮肤科医生的处方。在治疗选择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理学选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
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.
期刊最新文献
[Translated article] Is patient safety still a strategic priority? Is patient safety still a strategic priority? [Translated article] Multidrug-resistant extra-pulmonary tuberculosis in a hemodialysis patient treated with bedaquiline and tedizolid. A case report and a literature review. Adequacy of three-compartment parenteral nutrition bags to current European guidelines for adults: a simulation study. Making research accessible, breaking down barriers: the new frontier of clinical trials.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1