Literature DB >> 34434292

The use of rapamycin to treat vascular tumours and malformations: A single-centre experience.

Soumitra Tole1, Michelle Fantauzzi2, Diana Cottingham3, Joao G Amaral4, Philip R John4, Irene Lara-Corrales5, Elena Pope5, Manuel D Carcao1,6.   

Abstract

OBJECTIVES: To assess the safety and efficacy of rapamycin in treating children with vascular tumours and malformations. STUDY
DESIGN: We performed a retrospective review at a large tertiary care paediatric centre to assess the efficacy and safety of using rapamycin to treat vascular tumours and malformations. Response to therapy was defined by patient-reported symptom improvement, radiological reduction in size of lesions, and/or improvement of laboratory parameters.
RESULTS: Forty-two patients (7 with vascular tumours and 35 with vascular malformations) have been treated with rapamycin. Despite 33 of 42 patients being diagnosed in the first year of life, the median age of initiating rapamycin was 11 years. Of the 38 children treated for a minimum of 4 months, 29 (76%) exhibited a clinical response. Twenty-one patients had follow-up imaging studies and of these, 16 (76%) had radiographic decrease in lesion size. Median time to demonstration of response was 49 days. All five children with vascular tumours and all three children with vascular malformations under the age of 4 years showed a clinical response. Response rate was lower for children ≥ 4 years of age (0/2, 0% for vascular tumours; 21/28, 75% for vascular malformations). No patient experienced an infection directly related to rapamycin or discontinued rapamycin due to toxicity.
CONCLUSIONS: Rapamycin is safe and efficacious in most children with select vascular tumours and malformations. Young children appear to respond better, suggesting that early initiation of rapamycin should be considered.
© The Author(s) 2019. Published by Oxford University Press on behalf of the Canadian Paediatric Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Entities:  

Keywords:  Rapamycin; Sirolimus; Vascular malformation; Vascular tumour

Year:  2019        PMID: 34434292      PMCID: PMC8381855          DOI: 10.1093/pch/pxz090

Source DB:  PubMed          Journal:  Paediatr Child Health        ISSN: 1205-7088            Impact factor:   2.253


  18 in total

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Review 2.  mTOR signaling at a glance.

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3.  Vascular dysmorphogenesis caused by an activating mutation in the receptor tyrosine kinase TIE2.

Authors:  M Vikkula; L M Boon; K L Carraway; J T Calvert; A J Diamonti; B Goumnerov; K A Pasyk; D A Marchuk; M L Warman; L C Cantley; J B Mulliken; B R Olsen
Journal:  Cell       Date:  1996-12-27       Impact factor: 41.582

Review 4.  Medical management of vascular anomalies.

Authors:  Cameron C Trenor
Journal:  Semin Cutan Med Surg       Date:  2016-09

5.  Successful Treatment of a Complex Vascular Malformation With Sirolimus and Surgical Resection.

Authors:  Dov C Goldenberg; Marcelo Carvas; Denise Adams; Marcelo Giannotti; Rolf Gemperli
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6.  Sirolimus as treatment for 19 patients with refractory cervicofacial lymphatic malformation.

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Journal:  Laryngoscope       Date:  2017-08-07       Impact factor: 3.325

7.  Sirolimus in the Treatment of Vascular Anomalies.

Authors:  Paloma Triana; Mariela Dore; Vanesa Nuñez Cerezo; Manuel Cervantes; Alejandra Vilanova Sánchez; Miriam Miguel Ferrero; Mercedes Díaz González; Juan Carlos Lopez-Gutierrez
Journal:  Eur J Pediatr Surg       Date:  2016-10-10       Impact factor: 2.191

Review 8.  All roads lead to mTOR: integrating inflammation and tumor angiogenesis.

Authors:  Dung-Fang Lee; Mien-Chie Hung
Journal:  Cell Cycle       Date:  2007-09-20       Impact factor: 4.534

9.  Sirolimus for the treatment of children with various complicated vascular anomalies.

Authors:  Herwig Lackner; Anna Karastaneva; Wolfgang Schwinger; Martin Benesch; Petra Sovinz; Markus Seidel; Daniela Sperl; Sofia Lanz; Emir Haxhija; Friedrich Reiterer; Erich Sorantin; Christian E Urban
Journal:  Eur J Pediatr       Date:  2015-06-04       Impact factor: 3.183

10.  Sirolimus is efficacious in treatment for extensive and/or complex slow-flow vascular malformations: a monocentric prospective phase II study.

Authors:  Jennifer Hammer; Emmanuel Seront; Steven Duez; Sophie Dupont; An Van Damme; Sandra Schmitz; Claire Hoyoux; Caroline Chopinet; Philippe Clapuyt; Frank Hammer; Miikka Vikkula; Laurence M Boon
Journal:  Orphanet J Rare Dis       Date:  2018-10-29       Impact factor: 4.123

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