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Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study

BACKGROUND: Tuberous sclerosis complex (TSC) is a multisystem disease with prominent neurologic manifestations such as epilepsy, cognitive impairment and autism spectrum disorder. mTOR inhibitors have successfully been used to treat TSC-related manifestations in older children and adults. However, d...

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Autores principales: Saffari, Afshin, Brösse, Ines, Wiemer-Kruel, Adelheid, Wilken, Bernd, Kreuzaler, Paula, Hahn, Andreas, Bernhard, Matthias K., van Tilburg, Cornelis M., Hoffmann, Georg F., Gorenflo, Matthias, Hethey, Sven, Kaiser, Olaf, Kölker, Stefan, Wagner, Robert, Witt, Olaf, Merkenschlager, Andreas, Möckel, Andreas, Roser, Timo, Schlump, Jan-Ulrich, Serfling, Antje, Spiegler, Juliane, Milde, Till, Ziegler, Andreas, Syrbe, Steffen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6500021/
https://www.ncbi.nlm.nih.gov/pubmed/31053163
http://dx.doi.org/10.1186/s13023-019-1077-6
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author Saffari, Afshin
Brösse, Ines
Wiemer-Kruel, Adelheid
Wilken, Bernd
Kreuzaler, Paula
Hahn, Andreas
Bernhard, Matthias K.
van Tilburg, Cornelis M.
Hoffmann, Georg F.
Gorenflo, Matthias
Hethey, Sven
Kaiser, Olaf
Kölker, Stefan
Wagner, Robert
Witt, Olaf
Merkenschlager, Andreas
Möckel, Andreas
Roser, Timo
Schlump, Jan-Ulrich
Serfling, Antje
Spiegler, Juliane
Milde, Till
Ziegler, Andreas
Syrbe, Steffen
author_facet Saffari, Afshin
Brösse, Ines
Wiemer-Kruel, Adelheid
Wilken, Bernd
Kreuzaler, Paula
Hahn, Andreas
Bernhard, Matthias K.
van Tilburg, Cornelis M.
Hoffmann, Georg F.
Gorenflo, Matthias
Hethey, Sven
Kaiser, Olaf
Kölker, Stefan
Wagner, Robert
Witt, Olaf
Merkenschlager, Andreas
Möckel, Andreas
Roser, Timo
Schlump, Jan-Ulrich
Serfling, Antje
Spiegler, Juliane
Milde, Till
Ziegler, Andreas
Syrbe, Steffen
author_sort Saffari, Afshin
collection PubMed
description BACKGROUND: Tuberous sclerosis complex (TSC) is a multisystem disease with prominent neurologic manifestations such as epilepsy, cognitive impairment and autism spectrum disorder. mTOR inhibitors have successfully been used to treat TSC-related manifestations in older children and adults. However, data on their safety and efficacy in infants and young children are scarce. The objective of this study is to assess the utility and safety of mTOR inhibitor treatment in TSC patients under the age of 2 years. RESULTS: A total of 17 children (median age at study inclusion 2.4 years, range 0–6; 12 males, 5 females) with TSC who received early mTOR inhibitor therapy were studied. mTOR inhibitor treatment was started at a median age of 5 months (range 0–19 months). Reasons for initiation of treatment were cardiac rhabdomyomas (6 cases), subependymal giant cell astrocytomas (SEGA, 5 cases), combination of cardiac rhabdomyomas and SEGA (1 case), refractory epilepsy (4 cases) and disabling congenital focal lymphedema (1 case). In all cases everolimus was used. Everolimus therapy was overall well tolerated. Adverse events were classified according to the Common Terminology Criteria of Adverse Events (CTCAE, Version 5.0). Grade 1–2 adverse events occurred in 12 patients and included mild transient stomatitis (2 cases), worsening of infantile acne (1 case), increases of serum cholesterol and triglycerides (4 cases), changes in serum phosphate levels (2 cases), increase of cholinesterase (2 cases), transient neutropenia (2 cases), transient anemia (1 case), transient lymphopenia (1 case) and recurrent infections (7 cases). No grade 3–4 adverse events were reported. Treatment is currently continued in 13/17 patients. Benefits were reported in 14/17 patients and included decrease of cardiac rhabdomyoma size and improvement of arrhythmia, decrease of SEGA size, reduction of seizure frequency and regression of congenital focal lymphedema. Despite everolimus therapy, two patients treated for intractable epilepsy are still experiencing seizures and another one treated for SEGA showed no volume reduction. CONCLUSION: This retrospective multicenter study demonstrates that mTOR inhibitor treatment with everolimus is safe in TSC patients under the age of 2 years and shows beneficial effects on cardiac manifestations, SEGA size and early epilepsy.
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spelling pubmed-65000212019-05-09 Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study Saffari, Afshin Brösse, Ines Wiemer-Kruel, Adelheid Wilken, Bernd Kreuzaler, Paula Hahn, Andreas Bernhard, Matthias K. van Tilburg, Cornelis M. Hoffmann, Georg F. Gorenflo, Matthias Hethey, Sven Kaiser, Olaf Kölker, Stefan Wagner, Robert Witt, Olaf Merkenschlager, Andreas Möckel, Andreas Roser, Timo Schlump, Jan-Ulrich Serfling, Antje Spiegler, Juliane Milde, Till Ziegler, Andreas Syrbe, Steffen Orphanet J Rare Dis Research BACKGROUND: Tuberous sclerosis complex (TSC) is a multisystem disease with prominent neurologic manifestations such as epilepsy, cognitive impairment and autism spectrum disorder. mTOR inhibitors have successfully been used to treat TSC-related manifestations in older children and adults. However, data on their safety and efficacy in infants and young children are scarce. The objective of this study is to assess the utility and safety of mTOR inhibitor treatment in TSC patients under the age of 2 years. RESULTS: A total of 17 children (median age at study inclusion 2.4 years, range 0–6; 12 males, 5 females) with TSC who received early mTOR inhibitor therapy were studied. mTOR inhibitor treatment was started at a median age of 5 months (range 0–19 months). Reasons for initiation of treatment were cardiac rhabdomyomas (6 cases), subependymal giant cell astrocytomas (SEGA, 5 cases), combination of cardiac rhabdomyomas and SEGA (1 case), refractory epilepsy (4 cases) and disabling congenital focal lymphedema (1 case). In all cases everolimus was used. Everolimus therapy was overall well tolerated. Adverse events were classified according to the Common Terminology Criteria of Adverse Events (CTCAE, Version 5.0). Grade 1–2 adverse events occurred in 12 patients and included mild transient stomatitis (2 cases), worsening of infantile acne (1 case), increases of serum cholesterol and triglycerides (4 cases), changes in serum phosphate levels (2 cases), increase of cholinesterase (2 cases), transient neutropenia (2 cases), transient anemia (1 case), transient lymphopenia (1 case) and recurrent infections (7 cases). No grade 3–4 adverse events were reported. Treatment is currently continued in 13/17 patients. Benefits were reported in 14/17 patients and included decrease of cardiac rhabdomyoma size and improvement of arrhythmia, decrease of SEGA size, reduction of seizure frequency and regression of congenital focal lymphedema. Despite everolimus therapy, two patients treated for intractable epilepsy are still experiencing seizures and another one treated for SEGA showed no volume reduction. CONCLUSION: This retrospective multicenter study demonstrates that mTOR inhibitor treatment with everolimus is safe in TSC patients under the age of 2 years and shows beneficial effects on cardiac manifestations, SEGA size and early epilepsy. BioMed Central 2019-05-03 /pmc/articles/PMC6500021/ /pubmed/31053163 http://dx.doi.org/10.1186/s13023-019-1077-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Saffari, Afshin
Brösse, Ines
Wiemer-Kruel, Adelheid
Wilken, Bernd
Kreuzaler, Paula
Hahn, Andreas
Bernhard, Matthias K.
van Tilburg, Cornelis M.
Hoffmann, Georg F.
Gorenflo, Matthias
Hethey, Sven
Kaiser, Olaf
Kölker, Stefan
Wagner, Robert
Witt, Olaf
Merkenschlager, Andreas
Möckel, Andreas
Roser, Timo
Schlump, Jan-Ulrich
Serfling, Antje
Spiegler, Juliane
Milde, Till
Ziegler, Andreas
Syrbe, Steffen
Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study
title Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study
title_full Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study
title_fullStr Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study
title_full_unstemmed Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study
title_short Safety and efficacy of mTOR inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study
title_sort safety and efficacy of mtor inhibitor treatment in patients with tuberous sclerosis complex under 2 years of age – a multicenter retrospective study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6500021/
https://www.ncbi.nlm.nih.gov/pubmed/31053163
http://dx.doi.org/10.1186/s13023-019-1077-6
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