Eur J Pediatr Surg 2017; 27(01): 086-090
DOI: 10.1055/s-0036-1593383
Original Article
Georg Thieme Verlag KG Stuttgart · New York

Sirolimus in the Treatment of Vascular Anomalies

Paloma Triana
1   Department of Pediatric Surgery, Hospital Universitario La Paz, Madrid, Spain
,
Mariela Dore
1   Department of Pediatric Surgery, Hospital Universitario La Paz, Madrid, Spain
,
Vanesa Nuñez Cerezo
1   Department of Pediatric Surgery, Hospital Universitario La Paz, Madrid, Spain
,
Manuel Cervantes
1   Department of Pediatric Surgery, Hospital Universitario La Paz, Madrid, Spain
,
Alejandra Vilanova Sánchez
1   Department of Pediatric Surgery, Hospital Universitario La Paz, Madrid, Spain
,
Miriam Miguel Ferrero
2   Department of Plastic Pediatric Surgery, Hospital La Paz, Madrid, Spain
,
Mercedes Díaz González
2   Department of Plastic Pediatric Surgery, Hospital La Paz, Madrid, Spain
,
Juan Carlos Lopez-Gutierrez
2   Department of Plastic Pediatric Surgery, Hospital La Paz, Madrid, Spain
› Author Affiliations
Further Information

Publication History

15 May 2016

15 August 2016

Publication Date:
10 October 2016 (online)

Abstract

Aim of the Study mTOR inhibitors are showing promising results in the management of vascular anomalies. Although current controlled trials remain to be completed, many individual experiences are being published. We present our series of children with complex vascular anomalies treated with sirolimus.

Patients and Methods A retrospective review of 41 patients treated with sirolimus between January 2011 and December 2015 was performed: 15% (n = 6) had vascular tumors (4 kaposiform hemangioendotheliomas, 1 PTEN) and 85% (n = 35) had malformations (13 generalized lymphatic anomalies/Gorham–Stout diseases [GSD], 1 kaposiform lymphangiomatosis [KLA], 11 large lymphatic malformations (LMs) in critical areas, 2 lymphedemas, 4 venous malformations, and 4 aggressive arteriovenous malformations [AVM]). Several variables were collected: type of vascular anomaly, duration of treatment, dosage, response, and secondary effects.

Results There was a female predominance (1.4:1). All patients received sirolimus, at initial dosage of 0.8 mg/m2/12 hour. Overall successful response rate was 80.4% of cases, presenting improvement in radiologic imaging and reduction of symptoms, at a median time of 10 weeks. Patients showing no response included four AVMs, one GSD, one LM, one KLA, and one unknown tumor. Sirolimus was well tolerated, even in neonates, with insignificant side effects. No patients had complete resolution and no patients worsened on therapy. Thirty patients remain under treatment at the present moment.

Conclusion Sirolimus has become a new therapeutic option for patients with vascular anomalies that do not respond to other treatments. Unfortunately, important questions as what is the most appropriate dosage and for how long should the patient be treated remain unanswered. An international registry followed by customized controlled trials is mandatory to clarify the future of this therapy.

 
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