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Experience with the mTOR Inhibitor Everolimus in Pediatric Liver Graft Recipients
Introduction: Immunosuppression after pediatric liver transplantation remains a major challenge. MTOR inhibitors provide a promising therapeutic approach in combination with reduced CNI after transplantation. However, there are still few data regarding their use in children. Patients: We analyzed 37...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9955171/ https://www.ncbi.nlm.nih.gov/pubmed/36832496 http://dx.doi.org/10.3390/children10020367 |
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author | Wehming, Mathis Krebs-Schmitt, Dorothée Briem-Richter, Andrea Hegen, Bianca Brinkert, Florian Fischer, Lutz Grabhorn, Enke |
author_facet | Wehming, Mathis Krebs-Schmitt, Dorothée Briem-Richter, Andrea Hegen, Bianca Brinkert, Florian Fischer, Lutz Grabhorn, Enke |
author_sort | Wehming, Mathis |
collection | PubMed |
description | Introduction: Immunosuppression after pediatric liver transplantation remains a major challenge. MTOR inhibitors provide a promising therapeutic approach in combination with reduced CNI after transplantation. However, there are still few data regarding their use in children. Patients: We analyzed 37 patients with a median age of 10 years, who received Everolimus for one or more of the following indications: I = chronic graft dysfunction (n = 22); II = progressive renal impairment (n = 5); III = non-tolerable side effects with previous immunosuppressive medication (n = 6); and IV = malignancies (n = 10). The median follow-up time was 36 months. Results: Patient survival was 97%, and graft survival 84%, respectively. Stabilization of graft function was observed in 59% in subgroup 1, with 18.2% ultimately requiring retransplantation. No patient in subgroup IV developed recurrence of his primary tumor or PTLD by the endpoint of the study. Side effects were observed in 67.5% of the study patients, with infections being the most frequent (n = 20; 54.1%). There were no relevant effects on growth and development. Conclusion: Everolimus seems to be a treatment option in selected pediatric liver graft recipients for whom other regimens are not suitable. Overall, the efficacy was good and the side effect profile appeared to be acceptable. |
format | Online Article Text |
id | pubmed-9955171 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-99551712023-02-25 Experience with the mTOR Inhibitor Everolimus in Pediatric Liver Graft Recipients Wehming, Mathis Krebs-Schmitt, Dorothée Briem-Richter, Andrea Hegen, Bianca Brinkert, Florian Fischer, Lutz Grabhorn, Enke Children (Basel) Article Introduction: Immunosuppression after pediatric liver transplantation remains a major challenge. MTOR inhibitors provide a promising therapeutic approach in combination with reduced CNI after transplantation. However, there are still few data regarding their use in children. Patients: We analyzed 37 patients with a median age of 10 years, who received Everolimus for one or more of the following indications: I = chronic graft dysfunction (n = 22); II = progressive renal impairment (n = 5); III = non-tolerable side effects with previous immunosuppressive medication (n = 6); and IV = malignancies (n = 10). The median follow-up time was 36 months. Results: Patient survival was 97%, and graft survival 84%, respectively. Stabilization of graft function was observed in 59% in subgroup 1, with 18.2% ultimately requiring retransplantation. No patient in subgroup IV developed recurrence of his primary tumor or PTLD by the endpoint of the study. Side effects were observed in 67.5% of the study patients, with infections being the most frequent (n = 20; 54.1%). There were no relevant effects on growth and development. Conclusion: Everolimus seems to be a treatment option in selected pediatric liver graft recipients for whom other regimens are not suitable. Overall, the efficacy was good and the side effect profile appeared to be acceptable. MDPI 2023-02-13 /pmc/articles/PMC9955171/ /pubmed/36832496 http://dx.doi.org/10.3390/children10020367 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Wehming, Mathis Krebs-Schmitt, Dorothée Briem-Richter, Andrea Hegen, Bianca Brinkert, Florian Fischer, Lutz Grabhorn, Enke Experience with the mTOR Inhibitor Everolimus in Pediatric Liver Graft Recipients |
title | Experience with the mTOR Inhibitor Everolimus in Pediatric Liver Graft Recipients |
title_full | Experience with the mTOR Inhibitor Everolimus in Pediatric Liver Graft Recipients |
title_fullStr | Experience with the mTOR Inhibitor Everolimus in Pediatric Liver Graft Recipients |
title_full_unstemmed | Experience with the mTOR Inhibitor Everolimus in Pediatric Liver Graft Recipients |
title_short | Experience with the mTOR Inhibitor Everolimus in Pediatric Liver Graft Recipients |
title_sort | experience with the mtor inhibitor everolimus in pediatric liver graft recipients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9955171/ https://www.ncbi.nlm.nih.gov/pubmed/36832496 http://dx.doi.org/10.3390/children10020367 |
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