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在一名去势抵抗性转移性前列腺癌患者中,卡马西平的使用导致阿比特龙暴露量出现临床相关下降。

A clinically relevant decrease in abiraterone exposure associated with carbamazepine use in a patient with castration-resistant metastatic prostate cancer.

机构信息

Department of Pharmacy, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.

Department of Urology, Radboud Institute for Health Sciences, Radboud University Medical Center, Nijmegen, The Netherlands.

出版信息

Br J Clin Pharmacol. 2018 May;84(5):1064-1067. doi: 10.1111/bcp.13532. Epub 2018 Feb 21.

Abstract

ADVERSE EVENT

Decreased abiraterone exposure after introducing carbamazepine.

DRUGS IMPLICATED

Abiraterone acetate and carbamazepine.

THE PATIENT

A 65-year-old man with metastatic castration resistant prostate cancer, was treated with abiraterone acetate and prednisolone, and received concomitant carbamazepine for treatment of facial neuropathy.

EVIDENCE THAT LINKS THE DRUG TO THE EVENT

The interaction was confirmed by a decrease in abiraterone exposure >2-fold (area-under-the-curve and trough levels). After discontinuation of carbamazepine therapy, the abiraterone exposure normalized. No alternative causes were found that explain the decrease in abiraterone exposure.

MECHANISM

Induction of CYP3A and potentially phase I metabolism (SULT2A1) by carbamazepine.

IMPLICATIONS FOR THERAPY

Clinicians and pharmacists should be aware of this clinically relevant interaction. The national drug-drug interaction checker does not warn for this interaction, whereas both the Lexicomp® and Micromedex® advice to avoid if possible or to increase the abiraterone dose frequency to twice daily. Carbamazepine should not be combined with abiraterone to avoid underexposure and suboptimal therapy. Therapeutic drug monitoring of abiraterone is useful to guide therapy when drug-drug interactions cannot be avoided.

摘要

不良事件

卡马西平引入后阿比特龙暴露量减少。

涉及药物

阿比特龙醋酸酯和卡马西平。

患者

一名 65 岁男性,患有转移性去势抵抗性前列腺癌,接受阿比特龙醋酸酯和泼尼松龙治疗,并同时接受卡马西平治疗面部神经病变。

将药物与事件联系起来的证据

通过阿比特龙暴露量减少>2 倍(曲线下面积和谷值水平)确认了这种相互作用。停用卡马西平治疗后,阿比特龙的暴露量恢复正常。未发现其他可解释阿比特龙暴露量减少的原因。

机制

卡马西平诱导 CYP3A 和潜在的 I 相代谢(SULT2A1)。

治疗意义

临床医生和药剂师应意识到这种具有临床相关性的相互作用。国家药物相互作用检查器不会对此相互作用发出警告,而 Lexicomp® 和 Micromedex® 均建议如果可能的话避免使用,或增加阿比特龙的给药频率至每日两次。为避免暴露不足和治疗效果不佳,不应将卡马西平与阿比特龙联合使用。当无法避免药物相互作用时,阿比特龙的治疗药物监测有助于指导治疗。

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