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Feasibility study of short hydration using oral rehydration solution in cisplatin including chemotherapy of lung cancer

BACKGROUND: Cisplatin (CDDP) is used as a key anticancer drug for solid cancers, including lung cancer. However, a large quantity of fluid replacement is required to prevent renal dysfunction. This requirement have made outpatient chemotherapies including CDDP administration less popular among the a...

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Autores principales: Sato, Junya, Morikawa, Naoto, Nitanai, Hiroo, Nagashima, Hiromi, Nihei, Satoru, Yamauti, Kohei, Kudo, Kenzo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779197/
https://www.ncbi.nlm.nih.gov/pubmed/26949541
http://dx.doi.org/10.1186/s40780-016-0041-z
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author Sato, Junya
Morikawa, Naoto
Nitanai, Hiroo
Nagashima, Hiromi
Nihei, Satoru
Yamauti, Kohei
Kudo, Kenzo
author_facet Sato, Junya
Morikawa, Naoto
Nitanai, Hiroo
Nagashima, Hiromi
Nihei, Satoru
Yamauti, Kohei
Kudo, Kenzo
author_sort Sato, Junya
collection PubMed
description BACKGROUND: Cisplatin (CDDP) is used as a key anticancer drug for solid cancers, including lung cancer. However, a large quantity of fluid replacement is required to prevent renal dysfunction. This requirement have made outpatient chemotherapies including CDDP administration less popular among the available therapeutic options. We designed a short-term hydration regimen combined with oral rehydration solution (ORS) that has a supplementary water ability equivalent to intravenous electrolyte maintenance infusion and investigated its safety and feasibility in the CDDP including chemotherapy. METHODS: The subjects received chemotherapy including CDDP administration (60–80 mg/m(2)) for untreated lung cancer were recruited. The intravenous hydration was infused at around 2000 mL on Day 1, and patients drank ORS at a dose of 1000 mL/day for 3 days. Any renal dysfunction, gastrointestinal symptoms or other tolerability variables pertaining to the remaining three cycles of this regimen were analyzed in the patients who were able to continue treatment after the second cycle. RESULTS: The majority (29/35, 82.9 %) of patients completed intake of ORS for 3 days. The mean ± standard deviation of patient body-surface area-adjusted estimated glomerular filtration rate (eGFR), serum creatinine (sCre) and urea nitrogen from the initial therapy to 1 month after the last administration changed from 79.8 ± 11.7–67.0 ± 16.9 mL/min (p = 0.15), 0.70 ± 0.13–0.85 ± 0.27 mg/dL (p = 0.02), and 14.3 ± 3.8–17.1 ± 5.4 mg/dL (p = 0.09), respectively. The CTCAE ver 4.0 grades 1 or 2 adverse events pertaining to renal function after the last administration were 2 (5.7 %)/2 (5.7 %) patients assessed by sCre, and 14 (40.0 %)/12 (34.3 %) patients assessed by eGFR, respectively. There was no patient with ≥3 grade renal dysfunction based on either evaluation. CONCLUSIONS: Based on the results of this study, supplementary use of the ORS as a method of short-term hydration may be a feasible regimen for shortening infusion times and improving safety for those undergoing chemotherapy including CDDP administration.
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spelling pubmed-47791972016-03-06 Feasibility study of short hydration using oral rehydration solution in cisplatin including chemotherapy of lung cancer Sato, Junya Morikawa, Naoto Nitanai, Hiroo Nagashima, Hiromi Nihei, Satoru Yamauti, Kohei Kudo, Kenzo J Pharm Health Care Sci Research Article BACKGROUND: Cisplatin (CDDP) is used as a key anticancer drug for solid cancers, including lung cancer. However, a large quantity of fluid replacement is required to prevent renal dysfunction. This requirement have made outpatient chemotherapies including CDDP administration less popular among the available therapeutic options. We designed a short-term hydration regimen combined with oral rehydration solution (ORS) that has a supplementary water ability equivalent to intravenous electrolyte maintenance infusion and investigated its safety and feasibility in the CDDP including chemotherapy. METHODS: The subjects received chemotherapy including CDDP administration (60–80 mg/m(2)) for untreated lung cancer were recruited. The intravenous hydration was infused at around 2000 mL on Day 1, and patients drank ORS at a dose of 1000 mL/day for 3 days. Any renal dysfunction, gastrointestinal symptoms or other tolerability variables pertaining to the remaining three cycles of this regimen were analyzed in the patients who were able to continue treatment after the second cycle. RESULTS: The majority (29/35, 82.9 %) of patients completed intake of ORS for 3 days. The mean ± standard deviation of patient body-surface area-adjusted estimated glomerular filtration rate (eGFR), serum creatinine (sCre) and urea nitrogen from the initial therapy to 1 month after the last administration changed from 79.8 ± 11.7–67.0 ± 16.9 mL/min (p = 0.15), 0.70 ± 0.13–0.85 ± 0.27 mg/dL (p = 0.02), and 14.3 ± 3.8–17.1 ± 5.4 mg/dL (p = 0.09), respectively. The CTCAE ver 4.0 grades 1 or 2 adverse events pertaining to renal function after the last administration were 2 (5.7 %)/2 (5.7 %) patients assessed by sCre, and 14 (40.0 %)/12 (34.3 %) patients assessed by eGFR, respectively. There was no patient with ≥3 grade renal dysfunction based on either evaluation. CONCLUSIONS: Based on the results of this study, supplementary use of the ORS as a method of short-term hydration may be a feasible regimen for shortening infusion times and improving safety for those undergoing chemotherapy including CDDP administration. BioMed Central 2016-03-05 /pmc/articles/PMC4779197/ /pubmed/26949541 http://dx.doi.org/10.1186/s40780-016-0041-z 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, Junya
Morikawa, Naoto
Nitanai, Hiroo
Nagashima, Hiromi
Nihei, Satoru
Yamauti, Kohei
Kudo, Kenzo
Feasibility study of short hydration using oral rehydration solution in cisplatin including chemotherapy of lung cancer
title Feasibility study of short hydration using oral rehydration solution in cisplatin including chemotherapy of lung cancer
title_full Feasibility study of short hydration using oral rehydration solution in cisplatin including chemotherapy of lung cancer
title_fullStr Feasibility study of short hydration using oral rehydration solution in cisplatin including chemotherapy of lung cancer
title_full_unstemmed Feasibility study of short hydration using oral rehydration solution in cisplatin including chemotherapy of lung cancer
title_short Feasibility study of short hydration using oral rehydration solution in cisplatin including chemotherapy of lung cancer
title_sort feasibility study of short hydration using oral rehydration solution in cisplatin including chemotherapy of lung cancer
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779197/
https://www.ncbi.nlm.nih.gov/pubmed/26949541
http://dx.doi.org/10.1186/s40780-016-0041-z
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