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顺铂、卡铂和奥马铂的肾毒性及水化管理

Nephrotoxicity and hydration management for cisplatin, carboplatin, and ormaplatin.

作者信息

Cornelison T L, Reed E

机构信息

Medicine Branch, National Cancer Institute, Bethesda, Maryland 20892.

出版信息

Gynecol Oncol. 1993 Aug;50(2):147-58. doi: 10.1006/gyno.1993.1184.

Abstract

Renal toxicity is a prominent component of the toxicity profile of platinum-based chemotherapy. Kidney damage, once dose limiting for cisplatin, occurs in some patients who receive carboplatin and may occur with the third-generation platinum analog ormaplatin. Herein, we review what is known about the pathophysiology of therapy-induced renal toxicity for each of these agents and what is known about appropriate maneuvers to circumvent this toxicity. For cisplatin, hydration is always indicated and mannitol may be useful in selected settings. Furosemide is probably not generally useful. For carboplatin, hydration is important for patients with impaired renal function and for patients receiving high doses of drug (> or = 800 mg/m2). For ormplatin, renal toxicity appears not be prominent when hydration is administered in a fashion similar to cisplatin hydration. Detailed suggestions regarding the protection of kidney function when using these compounds are presented.

摘要

肾毒性是铂类化疗药物毒性特征的一个突出组成部分。肾脏损害曾是顺铂的剂量限制因素,在接受卡铂治疗的部分患者中也会出现,第三代铂类类似物奥马铂治疗时也可能发生。在此,我们综述了已知的这些药物所致治疗相关性肾毒性的病理生理学知识,以及已知的规避这种毒性的适当措施。对于顺铂,始终需要进行水化治疗,在特定情况下甘露醇可能有用。呋塞米一般可能无用。对于卡铂,肾功能受损的患者以及接受高剂量药物(≥800mg/m²)的患者进行水化治疗很重要。对于奥马铂,当以类似于顺铂水化的方式进行水化时,肾毒性似乎不突出。文中还给出了使用这些化合物时保护肾功能的详细建议。

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