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Nephrotoxicity of cancer therapeutic drugs: Focusing on novel agents

Kidney injury caused by anticancer agents is a common problem that can interfere with and affect the dose intensity of anticancer therapy, thus restricting patient survival. Recent advances in targeted and immunotherapeutic agents have transformed the landscape of medical oncology, and these agents...

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Autor principal: Hong, Min Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Nephrology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476309/
https://www.ncbi.nlm.nih.gov/pubmed/34233435
http://dx.doi.org/10.23876/j.krcp.21.037
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author Hong, Min Hee
author_facet Hong, Min Hee
author_sort Hong, Min Hee
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description Kidney injury caused by anticancer agents is a common problem that can interfere with and affect the dose intensity of anticancer therapy, thus restricting patient survival. Recent advances in targeted and immunotherapeutic agents have transformed the landscape of medical oncology, and these agents have been widely employed in clinical practice. While typically associated with favorable toxicity profiles, several novel anticancer drugs present distinctive nephrotoxicities. It remains urgent to closely monitor renal injuries associated with these agents, and medical practitioners should be familiar with general principles for managing nephrotoxicity associated with novel cancer drugs. This review provides an in-depth investigation of the literature and guidelines regarding the prevalence, clinical presentations, mechanisms, and management of nephrotoxicity for each drug.
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spelling pubmed-84763092021-10-07 Nephrotoxicity of cancer therapeutic drugs: Focusing on novel agents Hong, Min Hee Kidney Res Clin Pract Review Article Kidney injury caused by anticancer agents is a common problem that can interfere with and affect the dose intensity of anticancer therapy, thus restricting patient survival. Recent advances in targeted and immunotherapeutic agents have transformed the landscape of medical oncology, and these agents have been widely employed in clinical practice. While typically associated with favorable toxicity profiles, several novel anticancer drugs present distinctive nephrotoxicities. It remains urgent to closely monitor renal injuries associated with these agents, and medical practitioners should be familiar with general principles for managing nephrotoxicity associated with novel cancer drugs. This review provides an in-depth investigation of the literature and guidelines regarding the prevalence, clinical presentations, mechanisms, and management of nephrotoxicity for each drug. The Korean Society of Nephrology 2021-09 2021-06-23 /pmc/articles/PMC8476309/ /pubmed/34233435 http://dx.doi.org/10.23876/j.krcp.21.037 Text en Copyright © 2021 The Korean Society of Nephrology https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial and No Derivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) ) which permits unrestricted non-commercial use, distribution of the material without any modifications, and reproduction in any medium, provided the original works properly cited.
spellingShingle Review Article
Hong, Min Hee
Nephrotoxicity of cancer therapeutic drugs: Focusing on novel agents
title Nephrotoxicity of cancer therapeutic drugs: Focusing on novel agents
title_full Nephrotoxicity of cancer therapeutic drugs: Focusing on novel agents
title_fullStr Nephrotoxicity of cancer therapeutic drugs: Focusing on novel agents
title_full_unstemmed Nephrotoxicity of cancer therapeutic drugs: Focusing on novel agents
title_short Nephrotoxicity of cancer therapeutic drugs: Focusing on novel agents
title_sort nephrotoxicity of cancer therapeutic drugs: focusing on novel agents
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8476309/
https://www.ncbi.nlm.nih.gov/pubmed/34233435
http://dx.doi.org/10.23876/j.krcp.21.037
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