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Nephrotoxicity in cancer treatment: An overview

Anticancer drug nephrotoxicity is an important and increasing adverse drug event that limits the efficacy of cancer treatment. The kidney is an important elimination pathway for many antineoplastic drugs and their metabolites, which occurs by glomerular filtration and tubular secretion. Chemotherape...

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Autores principales: Santos, Maria Luísa Cordeiro, de Brito, Breno Bittencourt, da Silva, Filipe Antônio França, Botelho, Anelise Costa dos Santos, de Melo, Fabrício Freire
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7186234/
https://www.ncbi.nlm.nih.gov/pubmed/32355641
http://dx.doi.org/10.5306/wjco.v11.i4.190
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author Santos, Maria Luísa Cordeiro
de Brito, Breno Bittencourt
da Silva, Filipe Antônio França
Botelho, Anelise Costa dos Santos
de Melo, Fabrício Freire
author_facet Santos, Maria Luísa Cordeiro
de Brito, Breno Bittencourt
da Silva, Filipe Antônio França
Botelho, Anelise Costa dos Santos
de Melo, Fabrício Freire
author_sort Santos, Maria Luísa Cordeiro
collection PubMed
description Anticancer drug nephrotoxicity is an important and increasing adverse drug event that limits the efficacy of cancer treatment. The kidney is an important elimination pathway for many antineoplastic drugs and their metabolites, which occurs by glomerular filtration and tubular secretion. Chemotherapeutic agents, both conventional cytotoxic agents and molecularly targeted agents, can affect any segment of the nephron including its microvasculature, leading to many clinical manifestations such as proteinuria, hypertension, electrolyte disturbances, glomerulopathy, acute and chronic interstitial nephritis, acute kidney injury and at times chronic kidney disease. The clinician should be alert to recognize several factors that may maximize renal dysfunction and contribute to the increased incidence of nephrotoxicity associated with these drugs, such as intravascular volume depletion, the associated use of nonchemotherapeutic nephrotoxic drugs (analgesics, antibiotics, proton pump inhibitors, and bone-targeted therapies), radiographic ionic contrast media or radiation therapy, urinary tract obstruction, and intrinsic renal disease. Identification of patients at higher risk for nephrotoxicity may allow the prevention or at least reduction in the development and severity of this adverse effect. Therefore, the aim of this brief review is to provide currently available evidences on oncologic drug-related nephrotoxicity.
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spelling pubmed-71862342020-04-30 Nephrotoxicity in cancer treatment: An overview Santos, Maria Luísa Cordeiro de Brito, Breno Bittencourt da Silva, Filipe Antônio França Botelho, Anelise Costa dos Santos de Melo, Fabrício Freire World J Clin Oncol Minireviews Anticancer drug nephrotoxicity is an important and increasing adverse drug event that limits the efficacy of cancer treatment. The kidney is an important elimination pathway for many antineoplastic drugs and their metabolites, which occurs by glomerular filtration and tubular secretion. Chemotherapeutic agents, both conventional cytotoxic agents and molecularly targeted agents, can affect any segment of the nephron including its microvasculature, leading to many clinical manifestations such as proteinuria, hypertension, electrolyte disturbances, glomerulopathy, acute and chronic interstitial nephritis, acute kidney injury and at times chronic kidney disease. The clinician should be alert to recognize several factors that may maximize renal dysfunction and contribute to the increased incidence of nephrotoxicity associated with these drugs, such as intravascular volume depletion, the associated use of nonchemotherapeutic nephrotoxic drugs (analgesics, antibiotics, proton pump inhibitors, and bone-targeted therapies), radiographic ionic contrast media or radiation therapy, urinary tract obstruction, and intrinsic renal disease. Identification of patients at higher risk for nephrotoxicity may allow the prevention or at least reduction in the development and severity of this adverse effect. Therefore, the aim of this brief review is to provide currently available evidences on oncologic drug-related nephrotoxicity. Baishideng Publishing Group Inc 2020-04-24 2020-04-24 /pmc/articles/PMC7186234/ /pubmed/32355641 http://dx.doi.org/10.5306/wjco.v11.i4.190 Text en ©The Author(s) 2020. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Minireviews
Santos, Maria Luísa Cordeiro
de Brito, Breno Bittencourt
da Silva, Filipe Antônio França
Botelho, Anelise Costa dos Santos
de Melo, Fabrício Freire
Nephrotoxicity in cancer treatment: An overview
title Nephrotoxicity in cancer treatment: An overview
title_full Nephrotoxicity in cancer treatment: An overview
title_fullStr Nephrotoxicity in cancer treatment: An overview
title_full_unstemmed Nephrotoxicity in cancer treatment: An overview
title_short Nephrotoxicity in cancer treatment: An overview
title_sort nephrotoxicity in cancer treatment: an overview
topic Minireviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7186234/
https://www.ncbi.nlm.nih.gov/pubmed/32355641
http://dx.doi.org/10.5306/wjco.v11.i4.190
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