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Nephrotoxicity of cisplatin combination chemotherapy in thoracic malignancy patients with CKD risk factors

BACKGROUND: Nephrotoxicity is the major side effect that limits the dose of cisplatin that can be safely administered, and it is a clinical problem in cancer patients who received cisplatin combination chemotherapy. Recent evidence has demonstrated that patients with chronic kidney disease (CKD) hav...

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Autores principales: Sato, Ko, Watanabe, Satoshi, Ohtsubo, Aya, Shoji, Satoshi, Ishikawa, Daisuke, Tanaka, Tomohiro, Nozaki, Koichiro, Kondo, Rie, Okajima, Masaaki, Miura, Satoru, Tanaka, Junta, Sakagami, Takuro, Koya, Toshiyuki, Kagamu, Hiroshi, Yoshizawa, Hirohisa, Narita, Ichiei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793503/
https://www.ncbi.nlm.nih.gov/pubmed/26979596
http://dx.doi.org/10.1186/s12885-016-2271-8
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author Sato, Ko
Watanabe, Satoshi
Ohtsubo, Aya
Shoji, Satoshi
Ishikawa, Daisuke
Tanaka, Tomohiro
Nozaki, Koichiro
Kondo, Rie
Okajima, Masaaki
Miura, Satoru
Tanaka, Junta
Sakagami, Takuro
Koya, Toshiyuki
Kagamu, Hiroshi
Yoshizawa, Hirohisa
Narita, Ichiei
author_facet Sato, Ko
Watanabe, Satoshi
Ohtsubo, Aya
Shoji, Satoshi
Ishikawa, Daisuke
Tanaka, Tomohiro
Nozaki, Koichiro
Kondo, Rie
Okajima, Masaaki
Miura, Satoru
Tanaka, Junta
Sakagami, Takuro
Koya, Toshiyuki
Kagamu, Hiroshi
Yoshizawa, Hirohisa
Narita, Ichiei
author_sort Sato, Ko
collection PubMed
description BACKGROUND: Nephrotoxicity is the major side effect that limits the dose of cisplatin that can be safely administered, and it is a clinical problem in cancer patients who received cisplatin combination chemotherapy. Recent evidence has demonstrated that patients with chronic kidney disease (CKD) have an increased risk of developing acute kidney injury (AKI). The present study was conducted to evaluate the prevalence of CKD risk factors in patients who received cisplatin and to assess the correlation between CKD risk factors and cisplatin-induced AKI. METHODS: We retrospectively analyzed 84 patients treated with cisplatin combination chemotherapy for thoracic malignancies. AKI was defined as a decrease in the estimated glomerular filtration rate (eGFR) > 25 % from base line, an increase in the serum creatinine (sCre) level of > 0.3 mg/dl or ≥ 1.5 times the baseline level. RESULTS: Eighty of the 84 patients (95.2 %) had at least one risk factor for CKD. All enrolled patients received cisplatin with hydration, magnesium supplementation and mannitol. Cisplatin-induced AKI was observed in 18 patients (21.4 %). Univariate analysis revealed that cardiac disease and use of non-steroidal anti-inflammatory drugs (NSAIDs) were associated with cisplatin-induced nephrotoxicity (odds ratios [OR] 6 and 3.56, 95 % confidence intervals [CI] 1.21–29.87 and 1.11–11.39, p = 0.04 and p = 0.04, respectively). Multivariate analysis revealed that cisplatin nephrotoxicity occurred significantly more often in patients with both risk factors (OR 13.64, 95 % CI 1.11–326.83, p = 0.04). Patients with more risk factors for CKD tended to have a greater risk of developing cisplatin-induced AKI. CONCLUSIONS: We should consider avoiding administration of cisplatin to patients with CKD risk factors, particularly cardiac disease and NSAID use. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-016-2271-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-47935032016-03-16 Nephrotoxicity of cisplatin combination chemotherapy in thoracic malignancy patients with CKD risk factors Sato, Ko Watanabe, Satoshi Ohtsubo, Aya Shoji, Satoshi Ishikawa, Daisuke Tanaka, Tomohiro Nozaki, Koichiro Kondo, Rie Okajima, Masaaki Miura, Satoru Tanaka, Junta Sakagami, Takuro Koya, Toshiyuki Kagamu, Hiroshi Yoshizawa, Hirohisa Narita, Ichiei BMC Cancer Research Article BACKGROUND: Nephrotoxicity is the major side effect that limits the dose of cisplatin that can be safely administered, and it is a clinical problem in cancer patients who received cisplatin combination chemotherapy. Recent evidence has demonstrated that patients with chronic kidney disease (CKD) have an increased risk of developing acute kidney injury (AKI). The present study was conducted to evaluate the prevalence of CKD risk factors in patients who received cisplatin and to assess the correlation between CKD risk factors and cisplatin-induced AKI. METHODS: We retrospectively analyzed 84 patients treated with cisplatin combination chemotherapy for thoracic malignancies. AKI was defined as a decrease in the estimated glomerular filtration rate (eGFR) > 25 % from base line, an increase in the serum creatinine (sCre) level of > 0.3 mg/dl or ≥ 1.5 times the baseline level. RESULTS: Eighty of the 84 patients (95.2 %) had at least one risk factor for CKD. All enrolled patients received cisplatin with hydration, magnesium supplementation and mannitol. Cisplatin-induced AKI was observed in 18 patients (21.4 %). Univariate analysis revealed that cardiac disease and use of non-steroidal anti-inflammatory drugs (NSAIDs) were associated with cisplatin-induced nephrotoxicity (odds ratios [OR] 6 and 3.56, 95 % confidence intervals [CI] 1.21–29.87 and 1.11–11.39, p = 0.04 and p = 0.04, respectively). Multivariate analysis revealed that cisplatin nephrotoxicity occurred significantly more often in patients with both risk factors (OR 13.64, 95 % CI 1.11–326.83, p = 0.04). Patients with more risk factors for CKD tended to have a greater risk of developing cisplatin-induced AKI. CONCLUSIONS: We should consider avoiding administration of cisplatin to patients with CKD risk factors, particularly cardiac disease and NSAID use. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12885-016-2271-8) contains supplementary material, which is available to authorized users. BioMed Central 2016-03-15 /pmc/articles/PMC4793503/ /pubmed/26979596 http://dx.doi.org/10.1186/s12885-016-2271-8 Text en © Sato et al. 2016 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
Sato, Ko
Watanabe, Satoshi
Ohtsubo, Aya
Shoji, Satoshi
Ishikawa, Daisuke
Tanaka, Tomohiro
Nozaki, Koichiro
Kondo, Rie
Okajima, Masaaki
Miura, Satoru
Tanaka, Junta
Sakagami, Takuro
Koya, Toshiyuki
Kagamu, Hiroshi
Yoshizawa, Hirohisa
Narita, Ichiei
Nephrotoxicity of cisplatin combination chemotherapy in thoracic malignancy patients with CKD risk factors
title Nephrotoxicity of cisplatin combination chemotherapy in thoracic malignancy patients with CKD risk factors
title_full Nephrotoxicity of cisplatin combination chemotherapy in thoracic malignancy patients with CKD risk factors
title_fullStr Nephrotoxicity of cisplatin combination chemotherapy in thoracic malignancy patients with CKD risk factors
title_full_unstemmed Nephrotoxicity of cisplatin combination chemotherapy in thoracic malignancy patients with CKD risk factors
title_short Nephrotoxicity of cisplatin combination chemotherapy in thoracic malignancy patients with CKD risk factors
title_sort nephrotoxicity of cisplatin combination chemotherapy in thoracic malignancy patients with ckd risk factors
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4793503/
https://www.ncbi.nlm.nih.gov/pubmed/26979596
http://dx.doi.org/10.1186/s12885-016-2271-8
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