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Targeting the PD-1 pathway in pediatric solid tumors and brain tumors

While remarkable advances have been made in the treatment of pediatric leukemia over the past decades, new therapies are needed for children with advanced solid tumors and high-grade brain tumors who fail standard chemotherapy regimens. Immunotherapy with immune checkpoint inhibitors acting through...

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Detalles Bibliográficos
Autores principales: Wagner, Lars M, Adams, Val R
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396947/
https://www.ncbi.nlm.nih.gov/pubmed/28442918
http://dx.doi.org/10.2147/OTT.S124008
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author Wagner, Lars M
Adams, Val R
author_facet Wagner, Lars M
Adams, Val R
author_sort Wagner, Lars M
collection PubMed
description While remarkable advances have been made in the treatment of pediatric leukemia over the past decades, new therapies are needed for children with advanced solid tumors and high-grade brain tumors who fail standard chemotherapy regimens. Immunotherapy with immune checkpoint inhibitors acting through the programmed cell death-1 (PD-1) pathway has shown efficacy in some chemotherapy-resistant adult cancers, generating interest that these agents may also be helpful to treat certain refractory pediatric malignancies. In this manuscript we review current strategies for targeting the PD-1 pathway, highlighting putative biomarkers and the rationale for investigation of these drugs to treat common pediatric tumors such as sarcoma, neuroblastoma, and high-grade glioma. We summarize the completed and ongoing clinical trial data available, and suggest potential applications for further study.
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spelling pubmed-53969472017-04-25 Targeting the PD-1 pathway in pediatric solid tumors and brain tumors Wagner, Lars M Adams, Val R Onco Targets Ther Review While remarkable advances have been made in the treatment of pediatric leukemia over the past decades, new therapies are needed for children with advanced solid tumors and high-grade brain tumors who fail standard chemotherapy regimens. Immunotherapy with immune checkpoint inhibitors acting through the programmed cell death-1 (PD-1) pathway has shown efficacy in some chemotherapy-resistant adult cancers, generating interest that these agents may also be helpful to treat certain refractory pediatric malignancies. In this manuscript we review current strategies for targeting the PD-1 pathway, highlighting putative biomarkers and the rationale for investigation of these drugs to treat common pediatric tumors such as sarcoma, neuroblastoma, and high-grade glioma. We summarize the completed and ongoing clinical trial data available, and suggest potential applications for further study. Dove Medical Press 2017-04-12 /pmc/articles/PMC5396947/ /pubmed/28442918 http://dx.doi.org/10.2147/OTT.S124008 Text en © 2017 Wagner and Adams. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Wagner, Lars M
Adams, Val R
Targeting the PD-1 pathway in pediatric solid tumors and brain tumors
title Targeting the PD-1 pathway in pediatric solid tumors and brain tumors
title_full Targeting the PD-1 pathway in pediatric solid tumors and brain tumors
title_fullStr Targeting the PD-1 pathway in pediatric solid tumors and brain tumors
title_full_unstemmed Targeting the PD-1 pathway in pediatric solid tumors and brain tumors
title_short Targeting the PD-1 pathway in pediatric solid tumors and brain tumors
title_sort targeting the pd-1 pathway in pediatric solid tumors and brain tumors
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396947/
https://www.ncbi.nlm.nih.gov/pubmed/28442918
http://dx.doi.org/10.2147/OTT.S124008
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