• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

对依赖血液透析的肾功能不全患者采用基于卡铂的化疗并进行药代动力学分析。

Carboplatin-based chemotherapy with pharmacokinetic analysis for patients with hemodialysis-dependent renal insufficiency.

作者信息

Motzer R J, Niedzwiecki D, Isaacs M, Menendez-Botet C, Tong W P, Flombaum C, Scher H I, Bosl G J

机构信息

Genitourinary Oncology Service, Memorial Sloan-Kettering Cancer Center, New York, New York.

出版信息

Cancer Chemother Pharmacol. 1990;27(3):234-8. doi: 10.1007/BF00685719.

DOI:10.1007/BF00685719
PMID:2176133
Abstract

Three patients with renal insufficiency requiring hemodialysis were treated with carboplatin at 100 mg/m2 in combination with etoposide for advanced germ-cell tumor (GCT, two cases) or Adriamycin + vinblastine for a transitional-cell carcinoma of the ureter (one case). Hemodialysis was performed 24 h after the administration of carboplatin. Both patients with GCT achieved a complete response, and the patient with transitional-cell carcinoma of the ureter was inevaluable for response but his disease has not progressed. The dose of carboplatin was increased in one patient as renal function improved on therapy. In two patients, the pharmacokinetics of carboplatin were determined; the pre-dialysis half-lives, AUC, and total body clearances of free carboplatin-derived platinum were estimated to be 32 and 18.3 h, 4.93 and 6.17 mg ml-1 min, and 18.2 and 18.7 ml/min, respectively. The dialysis elimination half-lives (t1/2 beta) of 2 and 3 h, respectively, for these two patients were markedly lower than the predialysis values, indicating that carboplatin was dialyzed. In summary, carboplatin can be given to patients with severe renal insufficiency. Adequate AUCs were achieved and dialysis limited systemic exposure to free carboplatin.

摘要

三名需要血液透析的肾功能不全患者接受了卡铂治疗,剂量为100mg/m²,联合依托泊苷治疗晚期生殖细胞肿瘤(GCT,2例),或联合阿霉素+长春花碱治疗输尿管移行细胞癌(1例)。在给予卡铂24小时后进行血液透析。两名GCT患者均达到完全缓解,输尿管移行细胞癌患者的反应无法评估,但疾病未进展。一名患者在治疗过程中肾功能改善后增加了卡铂剂量。对两名患者测定了卡铂的药代动力学;透析前游离卡铂衍生铂的半衰期、AUC和全身清除率估计分别为32小时和18.3小时、4.93mg/ml·min和6.17mg/ml·min、18.2ml/min和18.7ml/min。这两名患者的透析清除半衰期(t1/2β)分别为2小时和3小时,明显低于透析前值,表明卡铂可被透析清除。总之,严重肾功能不全患者可以使用卡铂。可达到足够的AUC,透析限制了游离卡铂的全身暴露。

相似文献

1
Carboplatin-based chemotherapy with pharmacokinetic analysis for patients with hemodialysis-dependent renal insufficiency.对依赖血液透析的肾功能不全患者采用基于卡铂的化疗并进行药代动力学分析。
Cancer Chemother Pharmacol. 1990;27(3):234-8. doi: 10.1007/BF00685719.
2
[Pharmacokinetics of paclitaxel and carboplatin in a hemodialysis patient with metastatic urothelial carcinoma--a case report].
Gan To Kagaku Ryoho. 2003 Jul;30(7):1017-20.
3
Pharmacokinetics of carboplatin in a patient suffering from advanced ovarian carcinoma with hemodialysis-dependent renal insufficiency.
Nephron. 1994;66(2):157-61. doi: 10.1159/000187794.
4
Paclitaxel and carboplatin combination chemotherapy in a hemodialysis patient with advanced ovarian cancer.紫杉醇与卡铂联合化疗用于一名晚期卵巢癌血液透析患者
Gynecol Oncol. 2002 Feb;84(2):335-8. doi: 10.1006/gyno.2001.6527.
5
[Combination chemotherapy with carboplatin and etoposide against lung adenocarcinoma in a patient undergoing hemodialysis: a case report].[卡铂和依托泊苷联合化疗治疗一名接受血液透析的肺腺癌患者:病例报告]
Gan To Kagaku Ryoho. 1993 Dec;20(15):2409-11.
6
Pharmacokinetic analysis of carboplatin in patients with cancer who are undergoing hemodialysis.癌症患者血液透析时顺铂的药代动力学分析。
Cancer Chemother Pharmacol. 2010 Sep;66(4):813-7. doi: 10.1007/s00280-010-1366-1. Epub 2010 Jun 19.
7
Phase I trial with pharmacokinetic analyses of high-dose carboplatin, etoposide, and cyclophosphamide with autologous bone marrow transplantation in patients with refractory germ cell tumors.高剂量卡铂、依托泊苷和环磷酰胺联合自体骨髓移植治疗难治性生殖细胞肿瘤的Ⅰ期药代动力学分析试验。
Cancer Res. 1993 Aug 15;53(16):3730-5.
8
Pharmacokinetically guided dosing of carboplatin and etoposide during peritoneal dialysis and haemodialysis.腹膜透析和血液透析期间卡铂和依托泊苷的药代动力学指导给药
Br J Cancer. 1996 Mar;73(6):776-80. doi: 10.1038/bjc.1996.135.
9
[Pharmacokinetics of carboplatin in a patient under hemodialysis].
Gan To Kagaku Ryoho. 1994 Mar;21(4):547-50.
10
[Pharmacokinetics of cisplatin and methotrexate in a patient suffering from advanced ureteral tumor accompanied by chronic renal failure, undergoing combined hemodialysis and systemic M-VAC chemotherapy].
Gan To Kagaku Ryoho. 2000 Nov;27(13):2079-85.

引用本文的文献

1
Investigation of tolerability and quality of life for carboplatin-based chemotherapy in an elderly urothelial carcinoma patient undergoing hemodialysis: a case report.老年接受血液透析的尿路上皮癌患者基于卡铂化疗的耐受性及生活质量调查:一例报告
J Pharm Health Care Sci. 2018 Nov 29;4:29. doi: 10.1186/s40780-018-0124-0. eCollection 2018.
2
Successful delivery of chemotherapy to treat small-cell prostate cancer in a patient undergoing haemodialysis.在一名接受血液透析的患者中成功进行化疗以治疗小细胞前列腺癌。
Clin Kidney J. 2014 Dec;7(6):593-4. doi: 10.1093/ckj/sfu097. Epub 2014 Sep 16.
3
Dose adjustment of carboplatin in patients on hemodialysis.

本文引用的文献

1
Kinetics of cisplatin in an anuric patient undergoing hemofiltration dialysis.顺铂在接受血液滤过透析的无尿患者体内的动力学
Cancer Treat Rep. 1981 Jul-Aug;65(7-8):665-8.
2
Early clinical studies with cis-diammine-1,1-cyclobutane dicarboxylate platinum II.顺-二氨-1,1-环丁烷二羧酸铂II的早期临床研究。
Cancer Chemother Pharmacol. 1982;9(3):140-7. doi: 10.1007/BF00257742.
3
Pharmacokinetics of cis-diammine-1,1-cyclobutane dicarboxylate platinum(II) in patients with normal and impaired renal function.顺式-二氨-1,1-环丁烷二羧酸铂(II)在肾功能正常和受损患者中的药代动力学。
血液透析患者的卡铂剂量调整。
Med Oncol. 2014 Mar;31(3):848. doi: 10.1007/s12032-014-0848-0. Epub 2014 Jan 23.
4
Carboplatin pharmacokinetics in a patient receiving hemodialysis.接受血液透析患者的卡铂药代动力学
Pharmacotherapy. 2014 Feb;34(2):e9-13. doi: 10.1002/phar.1354. Epub 2013 Sep 14.
5
Pharmacokinetics of combination chemotherapy with paclitaxel and carboplatin in a patient with advanced epithelial ovarian cancer undergoing hemodialysis.晚期上皮性卵巢癌伴血液透析患者接受紫杉醇与卡铂联合化疗的药代动力学
Oncol Lett. 2010 May;1(3):511-513. doi: 10.3892/ol_00000090. Epub 2010 May 1.
6
Effect of haemodialysis on the pharmacokinetics of antineoplastic drugs.血液透析对抗肿瘤药物药代动力学的影响。
Clin Pharmacokinet. 2004;43(8):515-27. doi: 10.2165/00003088-200443080-00002.
7
Pharmacokinetically guided dosing of carboplatin and etoposide during peritoneal dialysis and haemodialysis.腹膜透析和血液透析期间卡铂和依托泊苷的药代动力学指导给药
Br J Cancer. 1996 Mar;73(6):776-80. doi: 10.1038/bjc.1996.135.
8
Clinical pharmacokinetics of carboplatin.卡铂的临床药代动力学
Clin Pharmacokinet. 1991 Oct;21(4):242-61. doi: 10.2165/00003088-199121040-00002.
9
Distribution characteristics of mitoxantrone in a patient undergoing hemodialysis.
Cancer Chemother Pharmacol. 1992;31(1):57-60. doi: 10.1007/BF00695995.
Cancer Res. 1984 Apr;44(4):1693-7.
4
A phase I and pharmacokinetic study of diamminecyclobutane-dicarboxylatoplatinum (NSC 241240).二胺环丁烷二羧酸铂(NSC 241240)的I期及药代动力学研究
Cancer Res. 1983 Sep;43(9):4470-3.
5
The growing teratoma syndrome.生长性畸胎瘤综合征
Cancer. 1982 Oct 15;50(8):1629-35. doi: 10.1002/1097-0142(19821015)50:8<1629::aid-cncr2820500828>3.0.co;2-1.
6
Changes in serum alpha-fetoprotein and chorionic gonadotropin in response to cancer therapy.血清甲胎蛋白和绒毛膜促性腺激素在癌症治疗后的变化。
Ann Clin Lab Sci. 1984 May-Jun;14(3):179-88.
7
Acute changes of alpha-fetoprotein and human chorionic gonadotropin during induction chemotherapy of germ cell tumors.生殖细胞肿瘤诱导化疗期间甲胎蛋白和人绒毛膜促性腺激素的急性变化
Cancer Res. 1982 Nov;42(11):4855-61.
8
Testicular cancer as a model for a curable neoplasm: The Richard and Hinda Rosenthal Foundation Award Lecture.睾丸癌作为可治愈肿瘤的模型:理查德与欣达·罗森塔尔基金会奖讲座
Cancer Res. 1981 Sep;41(9 Pt 1):3275-80.
9
Prospective validation of a pharmacologically based dosing scheme for the cis-diamminedichloroplatinum(II) analogue diamminecyclobutanedicarboxylatoplatinum.顺二氨二氯铂(II)类似物二氨环丁二羧酸铂基于药理学的给药方案的前瞻性验证
Cancer Res. 1985 Dec;45(12 Pt 1):6502-6.
10
Reappraisal of some dosage adjustment guidelines.对一些剂量调整指南的重新评估。
Cancer Treat Rep. 1987 Mar;71(3):229-33.