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The hubris and humility of cancer pharmacology in the post immuno‐oncology era

Cancer is a dreaded word, which has stimulated monumental efforts to discover and deliver effective cancer treatments for more than half a century. During the past two decades, our understanding of the molecular pathogenesis of cancer has increased remarkably. This has fostered an explosion in the n...

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Autor principal: Lazo, John S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783649/
https://www.ncbi.nlm.nih.gov/pubmed/31624635
http://dx.doi.org/10.1002/prp2.527
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author Lazo, John S.
author_facet Lazo, John S.
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description Cancer is a dreaded word, which has stimulated monumental efforts to discover and deliver effective cancer treatments for more than half a century. During the past two decades, our understanding of the molecular pathogenesis of cancer has increased remarkably. This has fostered an explosion in the number of experimental agents and clinical trials coupled with a dramatic rise in the regulatory approval of therapies for human cancers. Unfortunately, our preclinical models perform poorly as predictive platforms for the ultimate success of clinical candidates, reflecting the complexity of cancer. Moreover the common combination of cancer drugs prescribes the need for a better understanding of the fundamental pharmacology of each agent. Here I briefly outline some of the fundamental changes that have and have not occurred in cancer pharmacology during the past two decades and prognosticate on possible future directions.
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spelling pubmed-67836492019-10-17 The hubris and humility of cancer pharmacology in the post immuno‐oncology era Lazo, John S. Pharmacol Res Perspect Invited Reviews Cancer is a dreaded word, which has stimulated monumental efforts to discover and deliver effective cancer treatments for more than half a century. During the past two decades, our understanding of the molecular pathogenesis of cancer has increased remarkably. This has fostered an explosion in the number of experimental agents and clinical trials coupled with a dramatic rise in the regulatory approval of therapies for human cancers. Unfortunately, our preclinical models perform poorly as predictive platforms for the ultimate success of clinical candidates, reflecting the complexity of cancer. Moreover the common combination of cancer drugs prescribes the need for a better understanding of the fundamental pharmacology of each agent. Here I briefly outline some of the fundamental changes that have and have not occurred in cancer pharmacology during the past two decades and prognosticate on possible future directions. John Wiley and Sons Inc. 2019-10-08 /pmc/articles/PMC6783649/ /pubmed/31624635 http://dx.doi.org/10.1002/prp2.527 Text en © 2019 The Author. Pharmacology Research & Perspectives published by John Wiley & Sons Ltd, British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Invited Reviews
Lazo, John S.
The hubris and humility of cancer pharmacology in the post immuno‐oncology era
title The hubris and humility of cancer pharmacology in the post immuno‐oncology era
title_full The hubris and humility of cancer pharmacology in the post immuno‐oncology era
title_fullStr The hubris and humility of cancer pharmacology in the post immuno‐oncology era
title_full_unstemmed The hubris and humility of cancer pharmacology in the post immuno‐oncology era
title_short The hubris and humility of cancer pharmacology in the post immuno‐oncology era
title_sort hubris and humility of cancer pharmacology in the post immuno‐oncology era
topic Invited Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783649/
https://www.ncbi.nlm.nih.gov/pubmed/31624635
http://dx.doi.org/10.1002/prp2.527
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