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Clinical utility of nivolumab in the treatment of advanced melanoma

Melanomas are highly immunogenic tumors that evade the immune system by exploiting innate checkpoint pathways, rendering effector T-cells anergic. The immunotherapeutic approach of checkpoint inhibition can restore and invigorate endogenous antitumor T-cell responses and has become an important trea...

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Detalles Bibliográficos
Autores principales: Asmar, Ramsey, Yang, Jessica, Carvajal, Richard D
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778791/
https://www.ncbi.nlm.nih.gov/pubmed/27013881
http://dx.doi.org/10.2147/TCRM.S78039
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author Asmar, Ramsey
Yang, Jessica
Carvajal, Richard D
author_facet Asmar, Ramsey
Yang, Jessica
Carvajal, Richard D
author_sort Asmar, Ramsey
collection PubMed
description Melanomas are highly immunogenic tumors that evade the immune system by exploiting innate checkpoint pathways, rendering effector T-cells anergic. The immunotherapeutic approach of checkpoint inhibition can restore and invigorate endogenous antitumor T-cell responses and has become an important treatment option for patients with advanced melanoma. The CTLA-4 inhibitor ipilimumab and the PD-1 inhibitors nivolumab and pembrolizumab have been shown to induce durable responses and improve overall survival in metastatic, refractory melanoma. Optimization and validation of pretreatment biomarkers to predict response to these agents is a crucial area of ongoing research. Combination immunotherapy has recently demonstrated superior response rates compared to monotherapy; further investigation is needed to refine combinatorial strategies.
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spelling pubmed-47787912016-03-24 Clinical utility of nivolumab in the treatment of advanced melanoma Asmar, Ramsey Yang, Jessica Carvajal, Richard D Ther Clin Risk Manag Review Melanomas are highly immunogenic tumors that evade the immune system by exploiting innate checkpoint pathways, rendering effector T-cells anergic. The immunotherapeutic approach of checkpoint inhibition can restore and invigorate endogenous antitumor T-cell responses and has become an important treatment option for patients with advanced melanoma. The CTLA-4 inhibitor ipilimumab and the PD-1 inhibitors nivolumab and pembrolizumab have been shown to induce durable responses and improve overall survival in metastatic, refractory melanoma. Optimization and validation of pretreatment biomarkers to predict response to these agents is a crucial area of ongoing research. Combination immunotherapy has recently demonstrated superior response rates compared to monotherapy; further investigation is needed to refine combinatorial strategies. Dove Medical Press 2016-02-26 /pmc/articles/PMC4778791/ /pubmed/27013881 http://dx.doi.org/10.2147/TCRM.S78039 Text en © 2016 Asmar et al. 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
Asmar, Ramsey
Yang, Jessica
Carvajal, Richard D
Clinical utility of nivolumab in the treatment of advanced melanoma
title Clinical utility of nivolumab in the treatment of advanced melanoma
title_full Clinical utility of nivolumab in the treatment of advanced melanoma
title_fullStr Clinical utility of nivolumab in the treatment of advanced melanoma
title_full_unstemmed Clinical utility of nivolumab in the treatment of advanced melanoma
title_short Clinical utility of nivolumab in the treatment of advanced melanoma
title_sort clinical utility of nivolumab in the treatment of advanced melanoma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4778791/
https://www.ncbi.nlm.nih.gov/pubmed/27013881
http://dx.doi.org/10.2147/TCRM.S78039
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