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Controlling serum uric acid using febuxostat in cancer patients at risk of tumor lysis syndrome
Tumor lysis syndrome (TLS) is a life-threatening oncological emergency, in which control of serum uric acid (S-UA) levels is important. S-UA-lowering efficacy of a new xanthine oxidase inhibitor, febuxostat, was retrospectively evaluated in seven patients with hematological malignancies who were at...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156226/ https://www.ncbi.nlm.nih.gov/pubmed/25202361 http://dx.doi.org/10.3892/ol.2014.2394 |
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author | TAKAI, MIHOKO YAMAUCHI, TAKAHIRO FUJITA, KEI LEE, SHIN OOKURA, MIYUKI KISHI, SHINJI URASAKI, YOSHIMASA YOSHIDA, AKIRA IWASAKI, HIROMICHI UEDA, TAKANORI |
author_facet | TAKAI, MIHOKO YAMAUCHI, TAKAHIRO FUJITA, KEI LEE, SHIN OOKURA, MIYUKI KISHI, SHINJI URASAKI, YOSHIMASA YOSHIDA, AKIRA IWASAKI, HIROMICHI UEDA, TAKANORI |
author_sort | TAKAI, MIHOKO |
collection | PubMed |
description | Tumor lysis syndrome (TLS) is a life-threatening oncological emergency, in which control of serum uric acid (S-UA) levels is important. S-UA-lowering efficacy of a new xanthine oxidase inhibitor, febuxostat, was retrospectively evaluated in seven patients with hematological malignancies who were at an intermediate risk of developing TLS. A 10-mg dose of febuxostat was initiated and chemotherapy was started within 24 h of administering the first dose of febuxostat. Febuxostat was continued until at least day 7 of chemotherapy treatment. The UA-lowering treatment was considered effective if febuxostat reduced S-UA levels to ≤7.5 mg/dl by day 5. The mean S-UA level at base line was 6.4±2.6 mg/dl and, on day 5, the mean S-UA level was 4.7±1.8 mg/dl. All the patients achieved S-UA levels ≤7.5 mg/dl. Serum creatinine levels decreased from 0.93±0.25 to 0.85±0.25 mg/dl. The estimated glomerular filtration rate values increased from 69.7±24.5 to 76.9±26.2 ml/min. No adverse reactions were noted during the study period and no patients experienced progressive TLS. Successful control of S-UA and improved renal function were obtained in response to febuxostat treatment in cancer patients at a risk of TLS. |
format | Online Article Text |
id | pubmed-4156226 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-41562262014-09-08 Controlling serum uric acid using febuxostat in cancer patients at risk of tumor lysis syndrome TAKAI, MIHOKO YAMAUCHI, TAKAHIRO FUJITA, KEI LEE, SHIN OOKURA, MIYUKI KISHI, SHINJI URASAKI, YOSHIMASA YOSHIDA, AKIRA IWASAKI, HIROMICHI UEDA, TAKANORI Oncol Lett Articles Tumor lysis syndrome (TLS) is a life-threatening oncological emergency, in which control of serum uric acid (S-UA) levels is important. S-UA-lowering efficacy of a new xanthine oxidase inhibitor, febuxostat, was retrospectively evaluated in seven patients with hematological malignancies who were at an intermediate risk of developing TLS. A 10-mg dose of febuxostat was initiated and chemotherapy was started within 24 h of administering the first dose of febuxostat. Febuxostat was continued until at least day 7 of chemotherapy treatment. The UA-lowering treatment was considered effective if febuxostat reduced S-UA levels to ≤7.5 mg/dl by day 5. The mean S-UA level at base line was 6.4±2.6 mg/dl and, on day 5, the mean S-UA level was 4.7±1.8 mg/dl. All the patients achieved S-UA levels ≤7.5 mg/dl. Serum creatinine levels decreased from 0.93±0.25 to 0.85±0.25 mg/dl. The estimated glomerular filtration rate values increased from 69.7±24.5 to 76.9±26.2 ml/min. No adverse reactions were noted during the study period and no patients experienced progressive TLS. Successful control of S-UA and improved renal function were obtained in response to febuxostat treatment in cancer patients at a risk of TLS. D.A. Spandidos 2014-10 2014-07-30 /pmc/articles/PMC4156226/ /pubmed/25202361 http://dx.doi.org/10.3892/ol.2014.2394 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Articles TAKAI, MIHOKO YAMAUCHI, TAKAHIRO FUJITA, KEI LEE, SHIN OOKURA, MIYUKI KISHI, SHINJI URASAKI, YOSHIMASA YOSHIDA, AKIRA IWASAKI, HIROMICHI UEDA, TAKANORI Controlling serum uric acid using febuxostat in cancer patients at risk of tumor lysis syndrome |
title | Controlling serum uric acid using febuxostat in cancer patients at risk of tumor lysis syndrome |
title_full | Controlling serum uric acid using febuxostat in cancer patients at risk of tumor lysis syndrome |
title_fullStr | Controlling serum uric acid using febuxostat in cancer patients at risk of tumor lysis syndrome |
title_full_unstemmed | Controlling serum uric acid using febuxostat in cancer patients at risk of tumor lysis syndrome |
title_short | Controlling serum uric acid using febuxostat in cancer patients at risk of tumor lysis syndrome |
title_sort | controlling serum uric acid using febuxostat in cancer patients at risk of tumor lysis syndrome |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4156226/ https://www.ncbi.nlm.nih.gov/pubmed/25202361 http://dx.doi.org/10.3892/ol.2014.2394 |
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