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NFB-05. A family-centered neurocutaneous syndrome clinic in the age of targeted therapies

On April 10, 2020, the FDA approved selumetinib for the treatment of pediatric patients 2 years of age and older with neurofibromatosis type 1 who have symptomatic, inoperable plexiform neurofibromas. This, combined with the 2016 EXIST-3 data showing the efficacy of adjunctive everolimus in the trea...

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Autores principales: Marks, Asher, Antaya, Richard, Balsamo, Lyn, Cardinale, Kathleen, Cheron, Rebecca, Frumberg, David, Gentile, Victoria, Habib, Larissa, Puthenpura, Vidya, Zhang, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9165028/
http://dx.doi.org/10.1093/neuonc/noac079.469
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author Marks, Asher
Antaya, Richard
Balsamo, Lyn
Cardinale, Kathleen
Cheron, Rebecca
Frumberg, David
Gentile, Victoria
Habib, Larissa
Puthenpura, Vidya
Zhang, Hui
author_facet Marks, Asher
Antaya, Richard
Balsamo, Lyn
Cardinale, Kathleen
Cheron, Rebecca
Frumberg, David
Gentile, Victoria
Habib, Larissa
Puthenpura, Vidya
Zhang, Hui
author_sort Marks, Asher
collection PubMed
description On April 10, 2020, the FDA approved selumetinib for the treatment of pediatric patients 2 years of age and older with neurofibromatosis type 1 who have symptomatic, inoperable plexiform neurofibromas. This, combined with the 2016 EXIST-3 data showing the efficacy of adjunctive everolimus in the treatment of tuberous sclerosis associated seizures, have resulted in the re-imagining of the treatment of these neurocutaneous syndromes and subsequently, the multidisciplinary clinics in which they are treated. In early 2021, this reshaping resulted in the launch of a unique, family-centered clinic at Yale New Haven Children’s Hospital serving children and young adults up to 30 years of age in the management of NF1, NF2, tuberous sclerosis and schwannomatosis. Here we present the clinical reasoning and benefit of a multidisciplinary, family-centered clinic that manages to combine on-site, real-time access to neuro-oncology, neurology, psychology, dermatology, orthopedics, genetics, and ophthalmology. We will describe how the collaboration of these specialists is essential for providing high-quality, easy-access care to patients and families with the above noted syndromes – particularly with the advent of effective, readily available targeted therapies that carry their own side effects requiring further subspecialty consultation. Furthermore, we will describe previous and ongoing challenges to the creation of such a clinic and offer solutions based on our experience.
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spelling pubmed-91650282022-06-05 NFB-05. A family-centered neurocutaneous syndrome clinic in the age of targeted therapies Marks, Asher Antaya, Richard Balsamo, Lyn Cardinale, Kathleen Cheron, Rebecca Frumberg, David Gentile, Victoria Habib, Larissa Puthenpura, Vidya Zhang, Hui Neuro Oncol Neurofibromatosis and other Predisposition Syndromes On April 10, 2020, the FDA approved selumetinib for the treatment of pediatric patients 2 years of age and older with neurofibromatosis type 1 who have symptomatic, inoperable plexiform neurofibromas. This, combined with the 2016 EXIST-3 data showing the efficacy of adjunctive everolimus in the treatment of tuberous sclerosis associated seizures, have resulted in the re-imagining of the treatment of these neurocutaneous syndromes and subsequently, the multidisciplinary clinics in which they are treated. In early 2021, this reshaping resulted in the launch of a unique, family-centered clinic at Yale New Haven Children’s Hospital serving children and young adults up to 30 years of age in the management of NF1, NF2, tuberous sclerosis and schwannomatosis. Here we present the clinical reasoning and benefit of a multidisciplinary, family-centered clinic that manages to combine on-site, real-time access to neuro-oncology, neurology, psychology, dermatology, orthopedics, genetics, and ophthalmology. We will describe how the collaboration of these specialists is essential for providing high-quality, easy-access care to patients and families with the above noted syndromes – particularly with the advent of effective, readily available targeted therapies that carry their own side effects requiring further subspecialty consultation. Furthermore, we will describe previous and ongoing challenges to the creation of such a clinic and offer solutions based on our experience. Oxford University Press 2022-06-03 /pmc/articles/PMC9165028/ http://dx.doi.org/10.1093/neuonc/noac079.469 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Society for Neuro-Oncology. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Neurofibromatosis and other Predisposition Syndromes
Marks, Asher
Antaya, Richard
Balsamo, Lyn
Cardinale, Kathleen
Cheron, Rebecca
Frumberg, David
Gentile, Victoria
Habib, Larissa
Puthenpura, Vidya
Zhang, Hui
NFB-05. A family-centered neurocutaneous syndrome clinic in the age of targeted therapies
title NFB-05. A family-centered neurocutaneous syndrome clinic in the age of targeted therapies
title_full NFB-05. A family-centered neurocutaneous syndrome clinic in the age of targeted therapies
title_fullStr NFB-05. A family-centered neurocutaneous syndrome clinic in the age of targeted therapies
title_full_unstemmed NFB-05. A family-centered neurocutaneous syndrome clinic in the age of targeted therapies
title_short NFB-05. A family-centered neurocutaneous syndrome clinic in the age of targeted therapies
title_sort nfb-05. a family-centered neurocutaneous syndrome clinic in the age of targeted therapies
topic Neurofibromatosis and other Predisposition Syndromes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9165028/
http://dx.doi.org/10.1093/neuonc/noac079.469
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