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阿瑞匹坦的药代动力学及评估其对接受造血干细胞移植的癌症患者中环磷酰胺代谢的影响。

Aprepitant pharmacokinetics and assessing the impact of aprepitant on cyclophosphamide metabolism in cancer patients undergoing hematopoietic stem cell transplantation.

机构信息

Department of Pharmacy Practice, Oregon State University and Oregon Health & Science University, College of Pharmacy, Portland, OR 97239-4501, USA.

出版信息

J Clin Pharmacol. 2012 Apr;52(4):586-94. doi: 10.1177/0091270011398243. Epub 2011 Mar 17.

Abstract

Aprepitant, a neurokinin antagonist, is an effective antiemetic agent in chemotherapy for delayed nausea and vomiting. The study objective was to evaluate the pharmacokinetics of aprepitant and concurrent cyclophosphamide (CY), often a component of hematopoietic stem cell transplant (HSCT) conditioning regimen, in cancer patients undergoing HSCT. Forty subjects were randomized to either aprepitant or placebo in addition to standard antiemetics. Aprepitant or placebo was started 1 hour before the first chemotherapy or radiation dose for HSCT conditioning and administered daily until 4 days after infusion of the hematopoietic cell graft (for a total of 10-12 days). Serial blood samples were collected for aprepitant and CY plus 2 important CY metabolites. The results indicate that aprepitant is well absorbed and does not auto-induce its metabolism. No significant drug interaction was observed with CY or its metabolites. A significant portion of the patients had subtherapeutic aprepitant concentrations; however, chemotherapy-induced nausea and vomiting were effectively managed. No dosage adjustment was necessary, and administration of aprepitant in HSCT at the prescribed dosage of 125 mg orally on day 1 and 80 mg orally on each consecutive day through day +4 after HSCT was well tolerated with no significant changes in CY pharmacokinetic parameters.

摘要

阿瑞匹坦是一种神经激肽-1 拮抗剂,是化疗迟发性恶心和呕吐的有效止吐药。本研究旨在评估阿瑞匹坦与经常作为造血干细胞移植(HSCT)预处理方案组成部分的环磷酰胺(CY)在接受 HSCT 的癌症患者中的药代动力学。40 例患者随机分为阿瑞匹坦或安慰剂加标准止吐药组。阿瑞匹坦或安慰剂在 HSCT 预处理的第一剂化疗或放疗前 1 小时开始,并每天给药,直到造血细胞移植物输注后 4 天(共 10-12 天)。采集阿瑞匹坦和 CY 及其 2 种重要代谢物的连续血样。结果表明,阿瑞匹坦吸收良好,不会自动诱导其代谢。与 CY 或其代谢物无明显药物相互作用。尽管阿瑞匹坦的浓度低于治疗范围,但大部分患者的治疗仍有效。未观察到需要进行剂量调整,阿瑞匹坦在 HSCT 中的给药方案为第 1 天口服 125mg,随后每天口服 80mg,连续 4 天,直至 HSCT 后第 4 天,耐受良好,CY 药代动力学参数无明显变化。

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