Neirotti A, Barat V, Coppo P, La Selva R, Manicone R, Cotti R, Sensini M, Mussa A, Gatto M, Farri F, Basso M E, Fagioli F
Pediatric Onco-Hematology, Stem Cell Transplantation and Cellular Therapy Division, Regina Margherita Children's Hospital, Turin, Italy.
Pediatric Dermatology Unit, Regina Margherita Children's Hospital, Turin, Italy.
Front Pediatr. 2024 Jul 17;12:1434493. doi: 10.3389/fped.2024.1434493. eCollection 2024.
Vascular anomalies (VAs) constitute a heterogeneous group of tumors and malformations capable of inducing significant clinical events in specific patients, such as the compression of vital organs, pain, functional impairment, or acquired coagulopathy. Molecular investigations into the underlying mechanisms of VAs have unveiled the frequent involvement of the PI3 K/AKT/mTOR pathway. Sirolimus, a specific mTOR inhibitor, has emerged as a potential therapeutic agent; however, its routine clinical application in complex VAs is currently restricted by a lack of extensive clinical experience.
Between 2015 and 2024, we administered sirolimus to 14 pediatric patients with various types of vascular anomalies in two Italian centers, subjecting them to clinical and instrumental follow-up to investigate its efficacy and the possible occurrence of adverse events.
An overall improvement in or stability of their vascular anomalies was reported by 86% of patients. We also assessed toxicity, noting a low prevalence of life-threatening adverse events: only one case of sepsis was reported in a patient with a severe clinical condition, and four cases of recurrent aphthosis (28%) were reported. The most common side effect was dyslipidemia, with 43% of patients developing hypercholesterolemia (21%) or hypertriglyceridemia (21%), although these patients generally did not reach severe levels.
In line with data in the literature, according to our experience, medical therapy with sirolimus should be considered in pediatric patients affected by vascular anomalies.
血管异常(VAs)是一组异质性的肿瘤和畸形,能够在特定患者中引发重大临床事件,如重要器官受压、疼痛、功能障碍或获得性凝血病。对血管异常潜在机制的分子研究揭示了PI3 K/AKT/mTOR通路经常受累。西罗莫司是一种特异性mTOR抑制剂,已成为一种潜在的治疗药物;然而,目前其在复杂血管异常中的常规临床应用因缺乏广泛的临床经验而受到限制。
2015年至2024年期间,我们在意大利的两个中心对14例患有各种类型血管异常的儿科患者使用了西罗莫司,并对他们进行临床和仪器随访,以研究其疗效和可能出现的不良事件。
86%的患者报告其血管异常总体有所改善或保持稳定。我们还评估了毒性,注意到危及生命的不良事件发生率较低:仅1例患有严重临床疾病的患者报告发生败血症,4例报告复发性口疮(28%)。最常见的副作用是血脂异常,43%的患者出现高胆固醇血症(21%)或高甘油三酯血症(21%),不过这些患者的血脂水平一般未达到严重程度。
根据文献数据以及我们的经验,对于患有血管异常的儿科患者,应考虑使用西罗莫司进行药物治疗。