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A prospective randomized evaluation of three schedules of mesna administration in patients receiving an ifosfamide-containing chemotherapy regimen: sustained efficiency and simplified administration.在接受含异环磷酰胺化疗方案的患者中对三种美司钠给药方案进行的前瞻性随机评估:持续有效性和简化给药。
J Cancer Res Clin Oncol. 1995;121(2):128-31. doi: 10.1007/BF01202226.
2
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7
Prevention by 2-mercaptoethane sulfonate and N-acetylcysteine of renal oxidative damage in rats treated with ferric nitrilotriacetate.用2-巯基乙烷磺酸盐和N-乙酰半胱氨酸预防次氮基三乙酸铁处理的大鼠的肾脏氧化损伤。
Jpn J Cancer Res. 1996 Sep;87(9):882-6. doi: 10.1111/j.1349-7006.1996.tb02115.x.

本文引用的文献

1
Studies on the urotoxicity of oxazaphosphorine cytostatics and its prevention. 2. Comparative study on the uroprotective efficacy of thiols and other sulfur compounds.氧氮磷啶类细胞抑制剂的尿路毒性及其预防研究。2. 硫醇类及其他含硫化合物尿路保护疗效的比较研究。
Eur J Cancer Clin Oncol. 1981 Nov;17(11):1155-63.
2
Prevention of isophosphamide-induced urothelial toxicity with 2-mercaptoethane sulphonate sodium (mesnum) in patients with advanced carcinoma.2-巯基乙烷磺酸钠(美司钠)预防晚期癌症患者异环磷酰胺诱导的尿路上皮毒性
Lancet. 1980 Sep 27;2(8196):657-9. doi: 10.1016/s0140-6736(80)92703-8.
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Mesna--a short review.美司钠——简短综述。
Cancer Treat Rev. 1987 Jun;14(2):67-86. doi: 10.1016/0305-7372(87)90041-7.
4
The efficacy of mesna (2-mercaptoethane sodium sulfonate) as a uroprotectant in patients with hemorrhagic cystitis receiving further oxazaphosphorine chemotherapy.美司钠(2-巯基乙烷磺酸钠)作为尿路保护剂在接受进一步氮杂磷类化疗的出血性膀胱炎患者中的疗效。
J Clin Oncol. 1987 May;5(5):799-803. doi: 10.1200/JCO.1987.5.5.799.
5
Ifosfamide--pharmacologic overview.
Semin Oncol. 1989 Feb;16(1 Suppl 3):2-8.
6
Studies on the human pharmacokinetics of isophosphamide (NSC-109724).异环磷酰胺(NSC-109724)的人体药代动力学研究。
Cancer Treat Rep. 1976 Apr;60(4):451-8.
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Controlled clinical studies with an antidote against the urotoxicity of oxazaphosphorines: preliminary results.
Cancer Treat Rep. 1979 Mar;63(3):501-5.

在接受含异环磷酰胺化疗方案的患者中对三种美司钠给药方案进行的前瞻性随机评估:持续有效性和简化给药。

A prospective randomized evaluation of three schedules of mesna administration in patients receiving an ifosfamide-containing chemotherapy regimen: sustained efficiency and simplified administration.

作者信息

Katz A, Epelman S, Anelli A, Gorender E F, Cruz S M, Oliveira R M, Marques L A

机构信息

Department of Medical Oncology, A. C. Camargo Hospital, São Paulo, Brazil.

出版信息

J Cancer Res Clin Oncol. 1995;121(2):128-31. doi: 10.1007/BF01202226.

DOI:10.1007/BF01202226
PMID:7883776
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12201567/
Abstract

Chemotherapy with oxazaphosphorines, such as ifosfamide, is often limited by unacceptable urotoxicity. Without uroprotection hemorrhagic cystitis becomes dose-limiting. Mesna, a thiol compound, is a drug able to bind the toxic metabolites, forming nontoxic compounds in the urine. A total of 122 patients were enrolled in this study and 228 chemotherapy cycles with an ifosfamide-containing regimen were performed (225 evaluable). Mesna was given at the same total dose as the ifosfamide in all arms. On arm A, mesna was given i. v. in equal doses 15 min before and 4 h and 8 h following the ifosfamide dose. On arm B, mesna was given in three equivalent doses 15 min before (i.v.) and 4 h (i.v.) and 8 h (p.o., double dose) following ifosfamide. On arm C, mesna was given i.v. in two equal doses given 15 min before and 4 h following. The incidence of urotoxicity was very low (lower than 15%) in the three arms, 0% in A, 1.36% in B and 2.70% in C. All three arms were equally efficient. Schedule C was considered superior to the others, since it was equally effective, simpler and more convenient.

摘要

使用氧氮磷啶类药物进行化疗,如异环磷酰胺,常常受到难以接受的尿路毒性的限制。在没有尿路保护措施的情况下,出血性膀胱炎会成为剂量限制性因素。美司钠,一种硫醇化合物,是一种能够结合有毒代谢产物,在尿液中形成无毒化合物的药物。本研究共纳入122例患者,进行了228个含异环磷酰胺方案的化疗周期(225个可评估)。所有组中美司钠的总给药剂量与异环磷酰胺相同。在A组,美司钠在异环磷酰胺给药前15分钟、给药后4小时和8小时静脉注射等量剂量。在B组,美司钠在异环磷酰胺给药前15分钟(静脉注射)、给药后4小时(静脉注射)和8小时(口服,双倍剂量)分三次给予等量剂量。在C组,美司钠在异环磷酰胺给药前15分钟和给药后4小时静脉注射两个等量剂量。三组中尿路毒性的发生率非常低(低于15%),A组为0%,B组为1.36%,C组为2.70%。三组的疗效相同。C组方案被认为优于其他方案,因为它同样有效,更简单且更方便。