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Dose-related nephrotoxicity of carboplatin in children
This study investigated changes and the time course of these changes in renal function in children following treatment with carboplatin, and identified risk factors for nephrotoxicity. Glomerular and proximal renal tubular function were investigated before and up to 2 years after treatment in 23 chi...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1999
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362870/ https://www.ncbi.nlm.nih.gov/pubmed/10496362 http://dx.doi.org/10.1038/sj.bjc.6690697 |
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author | English, M W Skinner, R Pearson, A D J Price, L Wyllie, R Craft, A W |
author_facet | English, M W Skinner, R Pearson, A D J Price, L Wyllie, R Craft, A W |
author_sort | English, M W |
collection | PubMed |
description | This study investigated changes and the time course of these changes in renal function in children following treatment with carboplatin, and identified risk factors for nephrotoxicity. Glomerular and proximal renal tubular function were investigated before and up to 2 years after treatment in 23 children who received carboplatin. The main findings were reduced glomerular filtration rate (GFR), and increased renal tubular loss of magnesium, manifested by a low serum magnesium (S Mg). The mean fall in GFR was 22 ml min(−1) 1.73 m(−2) (P = 0.012), and in S Mg it was 0.17 mmol l(−1) (P = 0.0077). No patient had a clinically important reduction in GFR, and only one patient had symptomatic hypomagnesaemia. GFR and S Mg did not change over time after completion of treatment. Cumulative dose (CD) of carboplatin was inversely related to mean S Mg at the end of treatment (P = 0.031), and directly related to the fall in S Mg (P < 0.001). Calculated cumulative area under the plasma concentration versus time curve (AUC) of carboplatin was inversely related to S Mg after treatment (P = 0.004). Dose intensity (DI) of carboplatin was not shown to be related to S Mg following treatment. CD, AUC and DI of carboplatin were not related to GFR, nor change in GFR, after treatment. High CDs of carboplatin may be associated with evidence of renal damage qualitatively similar to but less severe than that caused by cisplatin. GFR and SMg should be carefully monitored when high CDs of carboplatin are used, or if carboplatin is combined with other nephrotoxic chemotherapy. © 1999 Cancer Research Campaign |
format | Text |
id | pubmed-2362870 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1999 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23628702009-09-10 Dose-related nephrotoxicity of carboplatin in children English, M W Skinner, R Pearson, A D J Price, L Wyllie, R Craft, A W Br J Cancer Regular Article This study investigated changes and the time course of these changes in renal function in children following treatment with carboplatin, and identified risk factors for nephrotoxicity. Glomerular and proximal renal tubular function were investigated before and up to 2 years after treatment in 23 children who received carboplatin. The main findings were reduced glomerular filtration rate (GFR), and increased renal tubular loss of magnesium, manifested by a low serum magnesium (S Mg). The mean fall in GFR was 22 ml min(−1) 1.73 m(−2) (P = 0.012), and in S Mg it was 0.17 mmol l(−1) (P = 0.0077). No patient had a clinically important reduction in GFR, and only one patient had symptomatic hypomagnesaemia. GFR and S Mg did not change over time after completion of treatment. Cumulative dose (CD) of carboplatin was inversely related to mean S Mg at the end of treatment (P = 0.031), and directly related to the fall in S Mg (P < 0.001). Calculated cumulative area under the plasma concentration versus time curve (AUC) of carboplatin was inversely related to S Mg after treatment (P = 0.004). Dose intensity (DI) of carboplatin was not shown to be related to S Mg following treatment. CD, AUC and DI of carboplatin were not related to GFR, nor change in GFR, after treatment. High CDs of carboplatin may be associated with evidence of renal damage qualitatively similar to but less severe than that caused by cisplatin. GFR and SMg should be carefully monitored when high CDs of carboplatin are used, or if carboplatin is combined with other nephrotoxic chemotherapy. © 1999 Cancer Research Campaign Nature Publishing Group 1999-09 /pmc/articles/PMC2362870/ /pubmed/10496362 http://dx.doi.org/10.1038/sj.bjc.6690697 Text en Copyright © 1999 Cancer Research Campaign https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Regular Article English, M W Skinner, R Pearson, A D J Price, L Wyllie, R Craft, A W Dose-related nephrotoxicity of carboplatin in children |
title | Dose-related nephrotoxicity of carboplatin in children |
title_full | Dose-related nephrotoxicity of carboplatin in children |
title_fullStr | Dose-related nephrotoxicity of carboplatin in children |
title_full_unstemmed | Dose-related nephrotoxicity of carboplatin in children |
title_short | Dose-related nephrotoxicity of carboplatin in children |
title_sort | dose-related nephrotoxicity of carboplatin in children |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2362870/ https://www.ncbi.nlm.nih.gov/pubmed/10496362 http://dx.doi.org/10.1038/sj.bjc.6690697 |
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