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An update on GM-CSF and its potential role in melanoma management

GM-CSF drives the differentiation of granulocytes and monocyte/macrophages from hematopoietic stem cell progenitors. It is required for differentiating monocytes into dendritic cells (DC). Although approved for recovery of granulocytes/monocytes in patients receiving chemotherapy, G-CSF is preferred...

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Detalles Bibliográficos
Autor principal: O Dillman, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Future Medicine Ltd 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7475793/
https://www.ncbi.nlm.nih.gov/pubmed/32922731
http://dx.doi.org/10.2217/mmt-2020-0011
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author O Dillman, Robert
author_facet O Dillman, Robert
author_sort O Dillman, Robert
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description GM-CSF drives the differentiation of granulocytes and monocyte/macrophages from hematopoietic stem cell progenitors. It is required for differentiating monocytes into dendritic cells (DC). Although approved for recovery of granulocytes/monocytes in patients receiving chemotherapy, G-CSF is preferred. Enthusiasm for GM-CSF monotherapy as a melanoma treatment was dampened by two large randomized trials. Although GM-CSF has been injected into tumors for many years, the efficacy of this has not been tested. There is a strong rationale for GM-CSF as a vaccine adjuvant, but it appears of benefit only for strategies that directly involve DCs, such as intratumor talimogene laherparepvec and vaccines in which DCs are loaded with antigen ex vivo and injected admixed with GM-CSF.
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spelling pubmed-74757932020-09-11 An update on GM-CSF and its potential role in melanoma management O Dillman, Robert Melanoma Manag Review GM-CSF drives the differentiation of granulocytes and monocyte/macrophages from hematopoietic stem cell progenitors. It is required for differentiating monocytes into dendritic cells (DC). Although approved for recovery of granulocytes/monocytes in patients receiving chemotherapy, G-CSF is preferred. Enthusiasm for GM-CSF monotherapy as a melanoma treatment was dampened by two large randomized trials. Although GM-CSF has been injected into tumors for many years, the efficacy of this has not been tested. There is a strong rationale for GM-CSF as a vaccine adjuvant, but it appears of benefit only for strategies that directly involve DCs, such as intratumor talimogene laherparepvec and vaccines in which DCs are loaded with antigen ex vivo and injected admixed with GM-CSF. Future Medicine Ltd 2020-07-29 /pmc/articles/PMC7475793/ /pubmed/32922731 http://dx.doi.org/10.2217/mmt-2020-0011 Text en © 2020 Robert O. Dillman This work is licensed under the Attribution-NonCommercial-NoDerivatives 4.0 Unported License (http://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Review
O Dillman, Robert
An update on GM-CSF and its potential role in melanoma management
title An update on GM-CSF and its potential role in melanoma management
title_full An update on GM-CSF and its potential role in melanoma management
title_fullStr An update on GM-CSF and its potential role in melanoma management
title_full_unstemmed An update on GM-CSF and its potential role in melanoma management
title_short An update on GM-CSF and its potential role in melanoma management
title_sort update on gm-csf and its potential role in melanoma management
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7475793/
https://www.ncbi.nlm.nih.gov/pubmed/32922731
http://dx.doi.org/10.2217/mmt-2020-0011
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