mTOR inhibitors in pediatric liver transplant recipients

被引:9
作者
Dumortier, Jerome [1 ,2 ]
Couchonnal, Eduardo [3 ]
Lacaille, Florence [4 ]
Rivet, Christine [3 ]
Debray, Dominique [4 ,5 ]
Boillot, Olivier [1 ,2 ]
Lachaux, Alain [2 ,3 ]
Ackermann, Oanez [6 ]
Gonzales, Emmanuel [6 ,7 ]
Wildhaber, Barbara E. [8 ]
Jacquemin, Emmanuel [6 ,7 ]
McLin, Valerie [8 ]
机构
[1] Hosp Civils Lyon, Edouard Herriot Hosp, Dept Digest Dis, F-69437 Lyon, France
[2] Univ Lyon, F-69008 Lyon, France
[3] Hosp Civils Lyon, Femme Mere Enfant Hosp, Dept Pediat Hepatogastroenterol & Nutr, F-69677 Lyon, France
[4] Necker Enfants Malad Hosp, AP HP, Natl Reference Ctr Rare Pediat Liver Dis, Pediat Hepatol Unit,Dept Pediat Gastroenterol & H, F-75015 Paris, France
[5] Univ Paris V, F-75006 Paris, France
[6] Bicetre Hosp, AP HP, Pediat Hepatol & Pediat Liver Transplantat Unit, Natl Reference Ctr Rare Pediat Liver Dis,Hepatino, F-94270 Le Kremlin Bicetre, France
[7] Univ Paris Sud 11, F-91400 Paris, France
[8] Univ Hosp Geneva, Swiss Ctr Liver Dis Children, CH-1205 Geneva, Switzerland
关键词
liver transplantation; pediatric; mTOR inhibitor; outcome; IMMUNOSUPPRESSIVE THERAPY; CALCINEURIN-INHIBITORS; EVEROLIMUS; CONVERSION; MULTICENTER; WITHDRAWAL; EFFICACY; SAFETY;
D O I
10.1016/j.clinre.2018.11.010
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: During the past decade, mTOR inhibitors (mTORi), everolimus and sirolimus, have been increasingly used after adult liver transplantation (LT). The aim of the present study was to describe the use of mTORi in pediatric LT recipients. Methods: All pediatric LT recipients who received mTORi before December 2017 from 4 European pediatric LT centers were included and analyzed. Results: The present retrospective study included 30 patients; 21 were male (70%), median age was 9.3 years (range: 1.2-17.1 years) at mTORi introduction. Main indications for mTORi introduction were pre-existing liver malignancy (43.3%), calcineurin inhibitor (CNI) nephrotoxicity (26.7%), or rejection (23.4%). At last follow-up, mTORi CNIs were withdrawn in 10 patients (10/29, 34.5%). The median dose of mTORi was 1.8 mg/day (range: 0.3-5.0) or 0.058 mg/kg/day (range: 0.01-0.26), and the median trough level was 5.1 mu g/L (range: 1.0-15.5). After a median follow-up of 2.8 years (range: 0.2-10.0), 50.0% of the patients presented with at leastone adverse event. The main adverse events included hyperlipidemia, proteinuria, dermatitis, and mucitis. Overall mTORi discontinuation rate was 23.3% (10.0% because of adverse event). Introduction of mTORi had no significant impact on renal function. Conclusion: Our results suggest that mTORi can be used in pediatric LT recipients in different clinical situations, both to reinforce immunosuppressive therapy, and to reduce CNI and relatedtoxicity. (C) 2018 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:403 / 409
页数:7
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