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Creating a comprehensive research strategy for cutaneous neurofibromas

OBJECTIVE: Outside of procedural-based methods, there are currently no established medical treatments for cutaneous neurofibroma (cNF), which afflict up to 99% of patients with NF1. Further, adult patients often report cNF are the greatest burden of living with NF1. The Neurofibromatosis Therapeutic...

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Autores principales: Blakeley, Jaishri O., Wolkenstein, Pierre, Widemann, Brigitte C., Lee, James, Le, Lu Q., Jackson, Rhonda, Stathis, Marigo, Verma, Sharad K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9703337/
https://www.ncbi.nlm.nih.gov/pubmed/29987129
http://dx.doi.org/10.1212/WNL.0000000000005789
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author Blakeley, Jaishri O.
Wolkenstein, Pierre
Widemann, Brigitte C.
Lee, James
Le, Lu Q.
Jackson, Rhonda
Stathis, Marigo
Verma, Sharad K.
author_facet Blakeley, Jaishri O.
Wolkenstein, Pierre
Widemann, Brigitte C.
Lee, James
Le, Lu Q.
Jackson, Rhonda
Stathis, Marigo
Verma, Sharad K.
author_sort Blakeley, Jaishri O.
collection PubMed
description OBJECTIVE: Outside of procedural-based methods, there are currently no established medical treatments for cutaneous neurofibroma (cNF), which afflict up to 99% of patients with NF1. Further, adult patients often report cNF are the greatest burden of living with NF1. The Neurofibromatosis Therapeutic Acceleration Program (NTAP) launched a think tank to address core questions to facilitate development of effective therapeutics for cNF in people with NF1. METHODS: Experts (with and without explicit experience with NF1 or cNF) from multiple scientific and medical disciplines, representing the ranks of academia, industry, and government agencies, were invited to become a member of a team addressing a specific subset of questions pertinent to cNF. Teams met monthly to review published and unpublished materials, and created summaries about the material known and unknown that may influence therapeutic development for cNF. Teams prioritized questions and organized supporting data, which was presented to the entire body of experts by each team at a research summit. RESULTS: Four themes were identified as being relevant to creating a comprehensive research strategy for cNF: (1) establishing definitions of cNF, (2) determining the biology of cNF with respect to tumor initiation, progression, and maintenance, (3) outlining the factors that guide therapies development, and (4) defining core considerations for clinical trials design and optimization for cNF. CONCLUSION: Considerations and key questions for each of the thematic areas were identified and provided basis for a request for applications launched by NTAP focused on cNF and are described in the accompanying articles of this supplement.
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spelling pubmed-97033372022-11-28 Creating a comprehensive research strategy for cutaneous neurofibromas Blakeley, Jaishri O. Wolkenstein, Pierre Widemann, Brigitte C. Lee, James Le, Lu Q. Jackson, Rhonda Stathis, Marigo Verma, Sharad K. Neurology Article OBJECTIVE: Outside of procedural-based methods, there are currently no established medical treatments for cutaneous neurofibroma (cNF), which afflict up to 99% of patients with NF1. Further, adult patients often report cNF are the greatest burden of living with NF1. The Neurofibromatosis Therapeutic Acceleration Program (NTAP) launched a think tank to address core questions to facilitate development of effective therapeutics for cNF in people with NF1. METHODS: Experts (with and without explicit experience with NF1 or cNF) from multiple scientific and medical disciplines, representing the ranks of academia, industry, and government agencies, were invited to become a member of a team addressing a specific subset of questions pertinent to cNF. Teams met monthly to review published and unpublished materials, and created summaries about the material known and unknown that may influence therapeutic development for cNF. Teams prioritized questions and organized supporting data, which was presented to the entire body of experts by each team at a research summit. RESULTS: Four themes were identified as being relevant to creating a comprehensive research strategy for cNF: (1) establishing definitions of cNF, (2) determining the biology of cNF with respect to tumor initiation, progression, and maintenance, (3) outlining the factors that guide therapies development, and (4) defining core considerations for clinical trials design and optimization for cNF. CONCLUSION: Considerations and key questions for each of the thematic areas were identified and provided basis for a request for applications launched by NTAP focused on cNF and are described in the accompanying articles of this supplement. Lippincott Williams & Wilkins 2018-07-10 /pmc/articles/PMC9703337/ /pubmed/29987129 http://dx.doi.org/10.1212/WNL.0000000000005789 Text en © 2018 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Blakeley, Jaishri O.
Wolkenstein, Pierre
Widemann, Brigitte C.
Lee, James
Le, Lu Q.
Jackson, Rhonda
Stathis, Marigo
Verma, Sharad K.
Creating a comprehensive research strategy for cutaneous neurofibromas
title Creating a comprehensive research strategy for cutaneous neurofibromas
title_full Creating a comprehensive research strategy for cutaneous neurofibromas
title_fullStr Creating a comprehensive research strategy for cutaneous neurofibromas
title_full_unstemmed Creating a comprehensive research strategy for cutaneous neurofibromas
title_short Creating a comprehensive research strategy for cutaneous neurofibromas
title_sort creating a comprehensive research strategy for cutaneous neurofibromas
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9703337/
https://www.ncbi.nlm.nih.gov/pubmed/29987129
http://dx.doi.org/10.1212/WNL.0000000000005789
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