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Lower blood pressure and risk of cisplatin nephrotoxicity: a retrospective cohort study
BACKGROUND: The pathophysiological mechanisms of cisplatin nephrotoxicity include the reduction of renal blood flow, as well as tubular epithelial cell toxicity. The objective of this study was to investigate the influence of lower blood pressure and decreased food intake on the incidence of cisplat...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319111/ https://www.ncbi.nlm.nih.gov/pubmed/28219368 http://dx.doi.org/10.1186/s12885-017-3135-6 |
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author | Komaki, Kazumi Kusaba, Tetsuro Tanaka, Mai Kado, Hiroshi Shiotsu, Yayoi Matsui, Masahiro Shiozaki, Atsushi Nakano, Hiroshi Ishikawa, Takeshi Fujiwara, Hitoshi Konishi, Hideyuki Itoh, Yoshito Matoba, Satoaki Tamagaki, Keiichi |
author_facet | Komaki, Kazumi Kusaba, Tetsuro Tanaka, Mai Kado, Hiroshi Shiotsu, Yayoi Matsui, Masahiro Shiozaki, Atsushi Nakano, Hiroshi Ishikawa, Takeshi Fujiwara, Hitoshi Konishi, Hideyuki Itoh, Yoshito Matoba, Satoaki Tamagaki, Keiichi |
author_sort | Komaki, Kazumi |
collection | PubMed |
description | BACKGROUND: The pathophysiological mechanisms of cisplatin nephrotoxicity include the reduction of renal blood flow, as well as tubular epithelial cell toxicity. The objective of this study was to investigate the influence of lower blood pressure and decreased food intake on the incidence of cisplatin nephrotoxicity. METHODS: We conducted a retrospective cohort study at a university hospital between 2011 and 2012. We identified hospitalized adult patients with head and neck cancer, esophageal cancer, or gastric cancer, who received intravenous cisplatin administration. The primary outcome was the incidence of cisplatin nephrotoxicity defined as the increase in serum creatinine after cisplatin administration more than 1.5 times from baseline. RESULTS: The study participants included 182 patients, in whom we observed a total of 442 cycles of cisplatin chemotherapy. The incidence of cisplatin nephrotoxicity was observed in 41 of 182 cycles with initial administration. Multivariate logistic regression analysis showed that systolic blood pressure was independently associated with cisplatin nephrotoxicity (adjusted odds ratio 0.75, 95% confidence interval 0.57 to 0.95 for each 10 mmHg). The use of renin-angiotensin system (RAS) inhibitors was also associated with cisplatin nephrotoxicity (3.39, 1.30 to 8.93). Among quartiles of systolic blood pressure in all cycles of chemotherapy, the incidence of nephrotoxicity in the lower blood pressure group was significantly higher than that in the higher blood pressure group for patients taking non-solid food (P = 0.037), while there was no significant difference for patients taking solid food (P = 0.67). CONCLUSIONS: Lower blood pressure and the use of RAS inhibitors were associated with the incidence of cisplatin nephrotoxicity, and lower blood pressure had a greater influence on nephrotoxicity in patients who could not take solid food. Discontinuation of antihypertensive medication including RAS inhibitors before cisplatin chemotherapy should be considered, which may be beneficial for patients with lower blood pressure. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-017-3135-6) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5319111 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53191112017-02-24 Lower blood pressure and risk of cisplatin nephrotoxicity: a retrospective cohort study Komaki, Kazumi Kusaba, Tetsuro Tanaka, Mai Kado, Hiroshi Shiotsu, Yayoi Matsui, Masahiro Shiozaki, Atsushi Nakano, Hiroshi Ishikawa, Takeshi Fujiwara, Hitoshi Konishi, Hideyuki Itoh, Yoshito Matoba, Satoaki Tamagaki, Keiichi BMC Cancer Research Article BACKGROUND: The pathophysiological mechanisms of cisplatin nephrotoxicity include the reduction of renal blood flow, as well as tubular epithelial cell toxicity. The objective of this study was to investigate the influence of lower blood pressure and decreased food intake on the incidence of cisplatin nephrotoxicity. METHODS: We conducted a retrospective cohort study at a university hospital between 2011 and 2012. We identified hospitalized adult patients with head and neck cancer, esophageal cancer, or gastric cancer, who received intravenous cisplatin administration. The primary outcome was the incidence of cisplatin nephrotoxicity defined as the increase in serum creatinine after cisplatin administration more than 1.5 times from baseline. RESULTS: The study participants included 182 patients, in whom we observed a total of 442 cycles of cisplatin chemotherapy. The incidence of cisplatin nephrotoxicity was observed in 41 of 182 cycles with initial administration. Multivariate logistic regression analysis showed that systolic blood pressure was independently associated with cisplatin nephrotoxicity (adjusted odds ratio 0.75, 95% confidence interval 0.57 to 0.95 for each 10 mmHg). The use of renin-angiotensin system (RAS) inhibitors was also associated with cisplatin nephrotoxicity (3.39, 1.30 to 8.93). Among quartiles of systolic blood pressure in all cycles of chemotherapy, the incidence of nephrotoxicity in the lower blood pressure group was significantly higher than that in the higher blood pressure group for patients taking non-solid food (P = 0.037), while there was no significant difference for patients taking solid food (P = 0.67). CONCLUSIONS: Lower blood pressure and the use of RAS inhibitors were associated with the incidence of cisplatin nephrotoxicity, and lower blood pressure had a greater influence on nephrotoxicity in patients who could not take solid food. Discontinuation of antihypertensive medication including RAS inhibitors before cisplatin chemotherapy should be considered, which may be beneficial for patients with lower blood pressure. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-017-3135-6) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-20 /pmc/articles/PMC5319111/ /pubmed/28219368 http://dx.doi.org/10.1186/s12885-017-3135-6 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Komaki, Kazumi Kusaba, Tetsuro Tanaka, Mai Kado, Hiroshi Shiotsu, Yayoi Matsui, Masahiro Shiozaki, Atsushi Nakano, Hiroshi Ishikawa, Takeshi Fujiwara, Hitoshi Konishi, Hideyuki Itoh, Yoshito Matoba, Satoaki Tamagaki, Keiichi Lower blood pressure and risk of cisplatin nephrotoxicity: a retrospective cohort study |
title | Lower blood pressure and risk of cisplatin nephrotoxicity: a retrospective cohort study |
title_full | Lower blood pressure and risk of cisplatin nephrotoxicity: a retrospective cohort study |
title_fullStr | Lower blood pressure and risk of cisplatin nephrotoxicity: a retrospective cohort study |
title_full_unstemmed | Lower blood pressure and risk of cisplatin nephrotoxicity: a retrospective cohort study |
title_short | Lower blood pressure and risk of cisplatin nephrotoxicity: a retrospective cohort study |
title_sort | lower blood pressure and risk of cisplatin nephrotoxicity: a retrospective cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319111/ https://www.ncbi.nlm.nih.gov/pubmed/28219368 http://dx.doi.org/10.1186/s12885-017-3135-6 |
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