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氟他胺和醋酸环丙孕酮疑似交叉肝毒性。

Suspected cross-hepatotoxicity of flutamide and cyproterone acetate.

作者信息

Miquel Mireia, Soler Aina, Vaqué Anna, Ojanguren Isabel, Costa Joan, Planas Ramon

机构信息

Servicio de Aparato Digestivo, Hospital Universitari Germans Trias y Pujol, Barcelona, Spain.

出版信息

Liver Int. 2007 Oct;27(8):1144-7. doi: 10.1111/j.1478-3231.2007.01549.x.

Abstract

Flutamide and cyproterone acetate (CPA) are both oral anti-androgens commonly used to treat advanced prostatic cancer. We report a case of drug-induced hepatotoxicity after consecutive treatment with flutamide and CPA. A 78-year-old male with advanced prostatic adenocarcinoma had been treated with flutamide 750 mg/day p.o. and leuproleride acetate 22.5 mg/3 months i.m. Three months later, the patient complained of choluria and jaundice. Laboratory examination revealed severe hepatocellular insufficiency. Flutamide-induced hepatotoxicity was suspected and therefore flutamide was withdrawn. His liver function abnormalities resolved after drug discontinuation. He was subsequently started on CPA 150 mg/day and again developed hepatotoxicity with severe hepatocellular impairment, which completely recovered after drug discontinuation. Other causes of acute liver failure were appropriately ruled out in both episodes and there was no evidence of active prostate cancer or liver metastases in both episodes. The occurrence of hepatotoxicity associated with flutamide and CPA on separated occasions suggests the possibility of a common mechanism of injury. It may become necessary to reassess the common practice of switching to another anti-androgen when hepatotoxicity appears. A closer monitoring of liver enzymes might be necessary in such cases, as an increased risk of a new severe hepatotoxicity event cannot be ruled out.

摘要

氟他胺和醋酸环丙孕酮(CPA)都是常用于治疗晚期前列腺癌的口服抗雄激素药物。我们报告一例在连续使用氟他胺和CPA治疗后发生药物性肝毒性的病例。一名78岁患有晚期前列腺腺癌的男性患者接受了口服氟他胺750毫克/天以及每3个月肌肉注射醋酸亮丙瑞林22.5毫克的治疗。三个月后,患者出现胆尿和黄疸。实验室检查显示严重的肝细胞功能不全。怀疑是氟他胺引起的肝毒性,因此停用了氟他胺。停药后他的肝功能异常得到缓解。随后他开始服用CPA 150毫克/天,再次出现肝毒性并伴有严重的肝细胞损伤,停药后完全康复。在这两个病例中均适当排除了急性肝衰竭的其他病因,且在这两个病例中均无前列腺癌活动或肝转移的证据。氟他胺和CPA在不同时间分别引发肝毒性,提示可能存在共同的损伤机制。当出现肝毒性时,可能有必要重新评估更换为另一种抗雄激素药物的常规做法。在这种情况下,可能需要更密切地监测肝酶,因为不能排除发生新的严重肝毒性事件的风险增加。

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