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Rare childhood cancers—an increasing entity requiring the need for global consensus and collaboration

Rare childhood cancers have not benefited to the same extent from the gains that have been made for their frequently occurring counterparts. In recent years, this gap has been recognized and a number of vehicles now exist to improve outcome, including rare tumor groups, disease-specific registries,...

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Detalles Bibliográficos
Autores principales: Kotecha, Rishi S, Kees, Ursula R, Cole, Catherine H, Gottardo, Nicholas G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4472204/
https://www.ncbi.nlm.nih.gov/pubmed/25664881
http://dx.doi.org/10.1002/cam4.426
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author Kotecha, Rishi S
Kees, Ursula R
Cole, Catherine H
Gottardo, Nicholas G
author_facet Kotecha, Rishi S
Kees, Ursula R
Cole, Catherine H
Gottardo, Nicholas G
author_sort Kotecha, Rishi S
collection PubMed
description Rare childhood cancers have not benefited to the same extent from the gains that have been made for their frequently occurring counterparts. In recent years, this gap has been recognized and a number of vehicles now exist to improve outcome, including rare tumor groups, disease-specific registries, and clinics. The multitude of approaches has allowed significant progress, however, this framework is limited by patient number and is not inclusive for every type of rare childhood cancer. These shortcomings can be overcome by a single global unified approach to the study of rare childhood tumors.
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spelling pubmed-44722042015-06-23 Rare childhood cancers—an increasing entity requiring the need for global consensus and collaboration Kotecha, Rishi S Kees, Ursula R Cole, Catherine H Gottardo, Nicholas G Cancer Med Cancer Research Rare childhood cancers have not benefited to the same extent from the gains that have been made for their frequently occurring counterparts. In recent years, this gap has been recognized and a number of vehicles now exist to improve outcome, including rare tumor groups, disease-specific registries, and clinics. The multitude of approaches has allowed significant progress, however, this framework is limited by patient number and is not inclusive for every type of rare childhood cancer. These shortcomings can be overcome by a single global unified approach to the study of rare childhood tumors. BlackWell Publishing Ltd 2015-06 2015-02-09 /pmc/articles/PMC4472204/ /pubmed/25664881 http://dx.doi.org/10.1002/cam4.426 Text en © 2015 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Cancer Research
Kotecha, Rishi S
Kees, Ursula R
Cole, Catherine H
Gottardo, Nicholas G
Rare childhood cancers—an increasing entity requiring the need for global consensus and collaboration
title Rare childhood cancers—an increasing entity requiring the need for global consensus and collaboration
title_full Rare childhood cancers—an increasing entity requiring the need for global consensus and collaboration
title_fullStr Rare childhood cancers—an increasing entity requiring the need for global consensus and collaboration
title_full_unstemmed Rare childhood cancers—an increasing entity requiring the need for global consensus and collaboration
title_short Rare childhood cancers—an increasing entity requiring the need for global consensus and collaboration
title_sort rare childhood cancers—an increasing entity requiring the need for global consensus and collaboration
topic Cancer Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4472204/
https://www.ncbi.nlm.nih.gov/pubmed/25664881
http://dx.doi.org/10.1002/cam4.426
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