非布司他对血液恶性肿瘤患者的癌症相关性高尿酸血症有用

K. Oiwa, M. Morita, Misato Kawamichi, K. Fujita, Shin Lee, E. Negoro, Miyuki Ookura, Yasufumi Matsuda, K. Tai, N. Hosono, T. Ueda, T. Yamauchi
{"title":"非布司他对血液恶性肿瘤患者的癌症相关性高尿酸血症有用","authors":"K. Oiwa, M. Morita, Misato Kawamichi, K. Fujita, Shin Lee, E. Negoro, Miyuki Ookura, Yasufumi Matsuda, K. Tai, N. Hosono, T. Ueda, T. Yamauchi","doi":"10.6032/GNAM.42.157","DOIUrl":null,"url":null,"abstract":"Tumor lysis syndrome(TLS)causes hyperuricemia in patients with malignancies under chemotherapeutic treatment. Lowering serum uric acid(S-UA)levels is the most important. Febuxostat has been officially used for chemotherapy-associated hyperuricemia since May 2016 in Japan. Rasburicase and febuxostat reduce S-UA. Rasburicase is effective for high-risk TLS, and febuxostat for low-intermediate risk. Here, febuxostat was evaluated as a treatment for cancer-related hyperuricemia after becoming officially employed for TLS(June 2016 November 2017). Sixty milligram was taken by mouth. The first chemotherapeutic treatment was started within a day after the first 60 mg dosing. The primary endpoint was S-UA normalization(≤ 7 mg /dL)on day 7 of chemotherapy. Twenty-four patients were evaluated(median : 70 years, range : 52-89 years, 14 males /10 females). The baseline S-UA was 7.2±2.7 mg /dL(mean±SD), and S-UA on the 7th day of chemotherapy was 2.5± 1.3 mg /dL(P<0.0001, by paired t-test). All patients met the primary endpoint. In addition, the baseline creatinine was 1.1±0.6 mg /dL(mean±SD), and the value on the 7th day of chemotherapy was 0.8±0.3 mg/dL(P=0.031, by paired t-test). Developing TLS was not observed. Severe adverse reactions were not noted. Thus, 60-mg febuxostat was effective against cancer-associated hyperuricemia. Introduction Tumor lysis syndrome(TLS)occurs in patients with malignancies when the first chemotherapeutic treatment is performed.15) From the cancer cells, purine nucleotides, proteins, phosphorus, and potassium, enter the bloodstream, which results in hyperuricemia, hyperkalemia, hyperphosphatemia, and hypocalcemia. These conditions may cause renal failure, arrhythmia, and ultimately death. The prevention and the prompt treatment of TLS are crucial. Guidelines and recommendations for the management of TLS have been published.2, 3, 6) There are laboratory and clinical forms of TLS.2, 3, 6) Laboratory TLS is diagnosed when two or more abnormal increases in serum values of uric acid(UA), potassium, or phosphorus are present. Clinical TLS requires, in addition to laboratory TLS, at least one of the followings ; kidney damage, arrhythmias, seizures, or death. The risk of TLS is classified into low受付:2018年2月13日,受理:2018年7月31日 1) Department of Hematology and Oncology 2) Department of Pharmacy, University of Fukui","PeriodicalId":12746,"journal":{"name":"GOUT AND NUCLEIC ACID METABOLISM","volume":"56 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-12-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Febuxostat is useful for cancer-associated hyperuricemia in patients with hematologic malignancies\",\"authors\":\"K. Oiwa, M. Morita, Misato Kawamichi, K. Fujita, Shin Lee, E. Negoro, Miyuki Ookura, Yasufumi Matsuda, K. Tai, N. Hosono, T. Ueda, T. Yamauchi\",\"doi\":\"10.6032/GNAM.42.157\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Tumor lysis syndrome(TLS)causes hyperuricemia in patients with malignancies under chemotherapeutic treatment. Lowering serum uric acid(S-UA)levels is the most important. Febuxostat has been officially used for chemotherapy-associated hyperuricemia since May 2016 in Japan. Rasburicase and febuxostat reduce S-UA. Rasburicase is effective for high-risk TLS, and febuxostat for low-intermediate risk. Here, febuxostat was evaluated as a treatment for cancer-related hyperuricemia after becoming officially employed for TLS(June 2016 November 2017). Sixty milligram was taken by mouth. The first chemotherapeutic treatment was started within a day after the first 60 mg dosing. The primary endpoint was S-UA normalization(≤ 7 mg /dL)on day 7 of chemotherapy. Twenty-four patients were evaluated(median : 70 years, range : 52-89 years, 14 males /10 females). The baseline S-UA was 7.2±2.7 mg /dL(mean±SD), and S-UA on the 7th day of chemotherapy was 2.5± 1.3 mg /dL(P<0.0001, by paired t-test). All patients met the primary endpoint. In addition, the baseline creatinine was 1.1±0.6 mg /dL(mean±SD), and the value on the 7th day of chemotherapy was 0.8±0.3 mg/dL(P=0.031, by paired t-test). Developing TLS was not observed. Severe adverse reactions were not noted. Thus, 60-mg febuxostat was effective against cancer-associated hyperuricemia. Introduction Tumor lysis syndrome(TLS)occurs in patients with malignancies when the first chemotherapeutic treatment is performed.15) From the cancer cells, purine nucleotides, proteins, phosphorus, and potassium, enter the bloodstream, which results in hyperuricemia, hyperkalemia, hyperphosphatemia, and hypocalcemia. These conditions may cause renal failure, arrhythmia, and ultimately death. The prevention and the prompt treatment of TLS are crucial. Guidelines and recommendations for the management of TLS have been published.2, 3, 6) There are laboratory and clinical forms of TLS.2, 3, 6) Laboratory TLS is diagnosed when two or more abnormal increases in serum values of uric acid(UA), potassium, or phosphorus are present. Clinical TLS requires, in addition to laboratory TLS, at least one of the followings ; kidney damage, arrhythmias, seizures, or death. The risk of TLS is classified into low受付:2018年2月13日,受理:2018年7月31日 1) Department of Hematology and Oncology 2) Department of Pharmacy, University of Fukui\",\"PeriodicalId\":12746,\"journal\":{\"name\":\"GOUT AND NUCLEIC ACID METABOLISM\",\"volume\":\"56 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-12-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"GOUT AND NUCLEIC ACID METABOLISM\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.6032/GNAM.42.157\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"GOUT AND NUCLEIC ACID METABOLISM","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.6032/GNAM.42.157","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

肿瘤溶解综合征(TLS)引起恶性肿瘤化疗患者高尿酸血症。降低血清尿酸(S-UA)水平是最重要的。非布司他于2016年5月在日本正式用于化疗相关高尿酸血症。Rasburicase和非布司他降低S-UA。Rasburicase对高风险TLS有效,非布司他对中低风险TLS有效。在这里,非布司他被正式用于TLS(2016年6月至2017年11月)后,被评估为癌症相关高尿酸血症的治疗方法。口服60毫克。第一次化疗在第一次60mg剂量后的一天内开始。主要终点为化疗第7天S-UA正常化(≤7 mg /dL)。24例患者被评估(中位:70岁,范围:52-89岁,14男/10女)。基线S-UA为7.2±2.7 mg /dL(mean±SD),化疗第7天S-UA为2.5±1.3 mg /dL(配对t检验P<0.0001)。所有患者均达到主要终点。基线肌酐为1.1±0.6 mg/dL(mean±SD),化疗第7天肌酐为0.8±0.3 mg/dL(配对t检验P=0.031)。未观察到发生TLS。未见严重不良反应。因此,60mg非布司他对癌症相关的高尿酸血症有效。肿瘤溶解综合征(TLS)发生在恶性肿瘤患者第一次化疗时。15)从癌细胞中,嘌呤核苷酸、蛋白质、磷和钾进入血液,导致高尿酸血症、高钾血症、高磷血症和低钙血症。这些情况可能导致肾功能衰竭、心律失常,最终导致死亡。TLS的预防和及时治疗至关重要。关于TLS管理的指南和建议已经发布。实验室TLS分为实验室和临床两种。当血清尿酸(UA)、钾或磷值出现两种或两种以上的异常升高时,可诊断为实验室TLS。除了实验室TLS外,临床TLS至少需要以下一项:肾损伤、心律失常、癫痫发作或死亡。TLS的风险分为低危、低危两类:1)福井大学血液肿瘤科2)药学系
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Febuxostat is useful for cancer-associated hyperuricemia in patients with hematologic malignancies
Tumor lysis syndrome(TLS)causes hyperuricemia in patients with malignancies under chemotherapeutic treatment. Lowering serum uric acid(S-UA)levels is the most important. Febuxostat has been officially used for chemotherapy-associated hyperuricemia since May 2016 in Japan. Rasburicase and febuxostat reduce S-UA. Rasburicase is effective for high-risk TLS, and febuxostat for low-intermediate risk. Here, febuxostat was evaluated as a treatment for cancer-related hyperuricemia after becoming officially employed for TLS(June 2016 November 2017). Sixty milligram was taken by mouth. The first chemotherapeutic treatment was started within a day after the first 60 mg dosing. The primary endpoint was S-UA normalization(≤ 7 mg /dL)on day 7 of chemotherapy. Twenty-four patients were evaluated(median : 70 years, range : 52-89 years, 14 males /10 females). The baseline S-UA was 7.2±2.7 mg /dL(mean±SD), and S-UA on the 7th day of chemotherapy was 2.5± 1.3 mg /dL(P<0.0001, by paired t-test). All patients met the primary endpoint. In addition, the baseline creatinine was 1.1±0.6 mg /dL(mean±SD), and the value on the 7th day of chemotherapy was 0.8±0.3 mg/dL(P=0.031, by paired t-test). Developing TLS was not observed. Severe adverse reactions were not noted. Thus, 60-mg febuxostat was effective against cancer-associated hyperuricemia. Introduction Tumor lysis syndrome(TLS)occurs in patients with malignancies when the first chemotherapeutic treatment is performed.15) From the cancer cells, purine nucleotides, proteins, phosphorus, and potassium, enter the bloodstream, which results in hyperuricemia, hyperkalemia, hyperphosphatemia, and hypocalcemia. These conditions may cause renal failure, arrhythmia, and ultimately death. The prevention and the prompt treatment of TLS are crucial. Guidelines and recommendations for the management of TLS have been published.2, 3, 6) There are laboratory and clinical forms of TLS.2, 3, 6) Laboratory TLS is diagnosed when two or more abnormal increases in serum values of uric acid(UA), potassium, or phosphorus are present. Clinical TLS requires, in addition to laboratory TLS, at least one of the followings ; kidney damage, arrhythmias, seizures, or death. The risk of TLS is classified into low受付:2018年2月13日,受理:2018年7月31日 1) Department of Hematology and Oncology 2) Department of Pharmacy, University of Fukui
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信