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A molecular and preclinical comparison of the PD-1–targeted T-cell checkpoint inhibitors nivolumab and pembrolizumab

T-cell checkpoint inhibition has a profound impact on cancer care and the programmed cell death protein 1 (PD-1)–targeted antibodies nivolumab and pembrolizumab have been two of the lead molecules of this therapeutic revolution. Their clinical comparability is a highly relevant topic of discussion,...

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Detalles Bibliográficos
Autores principales: Fessas, Petros, Lee, Hassal, Ikemizu, Shinji, Janowitz, Tobias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: W.B. Saunders 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612055/
https://www.ncbi.nlm.nih.gov/pubmed/28923212
http://dx.doi.org/10.1053/j.seminoncol.2017.06.002
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author Fessas, Petros
Lee, Hassal
Ikemizu, Shinji
Janowitz, Tobias
author_facet Fessas, Petros
Lee, Hassal
Ikemizu, Shinji
Janowitz, Tobias
author_sort Fessas, Petros
collection PubMed
description T-cell checkpoint inhibition has a profound impact on cancer care and the programmed cell death protein 1 (PD-1)–targeted antibodies nivolumab and pembrolizumab have been two of the lead molecules of this therapeutic revolution. Their clinical comparability is a highly relevant topic of discussion, but to a significant degree is a consequence of their molecular properties. Here we provide a molecular, preclinical, and early clinical comparison of the two antibodies, based on the available data and recent literature. We acknowledge the limitations of such comparisons, but suggest that based on the available data, differences in clinical trial outcomes between nivolumab and pembrolizumab are more likely drug-independent than drug-dependent.
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spelling pubmed-56120552017-09-29 A molecular and preclinical comparison of the PD-1–targeted T-cell checkpoint inhibitors nivolumab and pembrolizumab Fessas, Petros Lee, Hassal Ikemizu, Shinji Janowitz, Tobias Semin Oncol Article T-cell checkpoint inhibition has a profound impact on cancer care and the programmed cell death protein 1 (PD-1)–targeted antibodies nivolumab and pembrolizumab have been two of the lead molecules of this therapeutic revolution. Their clinical comparability is a highly relevant topic of discussion, but to a significant degree is a consequence of their molecular properties. Here we provide a molecular, preclinical, and early clinical comparison of the two antibodies, based on the available data and recent literature. We acknowledge the limitations of such comparisons, but suggest that based on the available data, differences in clinical trial outcomes between nivolumab and pembrolizumab are more likely drug-independent than drug-dependent. W.B. Saunders 2017-04 /pmc/articles/PMC5612055/ /pubmed/28923212 http://dx.doi.org/10.1053/j.seminoncol.2017.06.002 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Fessas, Petros
Lee, Hassal
Ikemizu, Shinji
Janowitz, Tobias
A molecular and preclinical comparison of the PD-1–targeted T-cell checkpoint inhibitors nivolumab and pembrolizumab
title A molecular and preclinical comparison of the PD-1–targeted T-cell checkpoint inhibitors nivolumab and pembrolizumab
title_full A molecular and preclinical comparison of the PD-1–targeted T-cell checkpoint inhibitors nivolumab and pembrolizumab
title_fullStr A molecular and preclinical comparison of the PD-1–targeted T-cell checkpoint inhibitors nivolumab and pembrolizumab
title_full_unstemmed A molecular and preclinical comparison of the PD-1–targeted T-cell checkpoint inhibitors nivolumab and pembrolizumab
title_short A molecular and preclinical comparison of the PD-1–targeted T-cell checkpoint inhibitors nivolumab and pembrolizumab
title_sort molecular and preclinical comparison of the pd-1–targeted t-cell checkpoint inhibitors nivolumab and pembrolizumab
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612055/
https://www.ncbi.nlm.nih.gov/pubmed/28923212
http://dx.doi.org/10.1053/j.seminoncol.2017.06.002
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