Literature DB >> 32044101

Effectiveness of sirolimus in the treatment of complex lymphatic malformations: Single center report of 56 cases.

Ruicheng Tian1, Yu Liang1, Weituo Zhang2, Jing Wang1, Yuhua Shan1, Hongxiang Gao1, Chenjie Xie1, Jingjing Li1, Min Xu3, Song Gu4.   

Abstract

BACKGROUND: Lymphatic malformations are common congenital vascular lesions. Neither surgical resection nor other surgical treatments have been found to be effective for invasive cases. Recent research has suggested that sirolimus is effective in treating complex lymphatic malformations (LMs). We aimed to evaluate the effectiveness and safety of oral sirolimus for children living with LMs in our hospital.
METHODS: Fifty-six cases of complex LMs treated with sirolimus were collected from Shanghai Children's Medical Centre between June 2016 and March 2019. All cases were confirmed either by pathology (44) or enhanced MRI (12). Following informed consent, sirolimus 0.8 mg/m2 bid was administered orally to participants and maintained at a trough concentration of 10-15 ng/ml. Children's ages at diagnosis were neonate to 16 years (mean 44.3 months). All children were followed up for 5 to 30 months, with a mean of 16.8 months.
RESULTS: During the follow-up period, blood, liver and kidney function as well as disseminated intravascular coagulation was regularly reviewed in all 56 children. Enhanced MRI was regularly performed to evaluate therapeutic effects. Total effective rate (complete response or partial response) of LMs was 89.3% (50/56). No serious adverse reactions were found.
CONCLUSION: This study suggests that sirolimus is effective and tolerable for decreasing lesions in children with complex LMs, leading to fewer and more tolerable side effects. There is no need to pursue an excision rate to reduce unnecessary operative complications since adjuvant sirolimus therapy modifies the complex LMs clinical appearance and alleviates their symptoms. TYPE OF STUDY: Clinical research. LEVEL OF EVIDENCE: Level IV.
Copyright © 2020 The Authors. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Generalized lymphatic anomaly; Lymphatic malformations; PIK3CA; Sirolimus; mTOR inhibitor

Mesh:

Substances:

Year:  2020        PMID: 32044101     DOI: 10.1016/j.jpedsurg.2019.12.021

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  4 in total

1.  Evaluation of Sirolimus Dosing in Neonates and Infants With Lymphatic Disorders: A Case Series.

Authors:  Jordan Serio; Sarah Gattoline; Hailey Collier; Anna Bustin
Journal:  J Pediatr Pharmacol Ther       Date:  2022-07-06

2.  Case Report: Reversible Hyperglycemia Following Rapamycin Treatment for Atypical Choroid Plexus Papilloma in an Infant.

Authors:  Jiale Liu; Minjie Luo; Siyuan Lv; Shaohua Tao; Zhu Wu; Lihua Yu; Danna Lin; Lulu Huang; Li Wu; Xu Liao; Juan Zi; Xiaorong Lai; Yuting Yuan; Wangming Zhang; Lihua Yang
Journal:  Front Endocrinol (Lausanne)       Date:  2022-07-05       Impact factor: 6.055

Review 3.  Neonatal vascular anomalies manifesting as soft-tissue masses.

Authors:  Nadeen Abu Ata; Adrienne M Hammill; Arnold C Merrow
Journal:  Pediatr Radiol       Date:  2021-08-10

Review 4.  Vascular endothelial cell specification in health and disease.

Authors:  Corina Marziano; Gael Genet; Karen K Hirschi
Journal:  Angiogenesis       Date:  2021-04-12       Impact factor: 9.596

  4 in total

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