Manso Gloria, Thole Zebron, Salgueiro Esther, Revuelta Pilar, Hidalgo Agustín
Centro de Farmacovigilancia de Asturias, Facultad de Medicina, Oviedo, Spain.
Pharmacoepidemiol Drug Saf. 2006 Apr;15(4):253-9. doi: 10.1002/pds.1168.
To analyse the type and main features of the hepatotoxicity induced by steroidal and non-steroidal antiandrogens spontaneously reported by physicians, pharmacists and nurses. This analysis could increase the information related to these adverse reactions mainly available from the published isolated cases.
Using the Spanish Pharmacovigilance database we searched for spontaneous reports recorded since the date of approval of each antiandrogen up to the present time. We analysed the frequency of liver disorders, the preferred terms coded, the presence of other hepatotoxic drugs, and the characteristics of cases of hepatitis.
Liver disorders were the most common adverse reactions associated with flutamide and bicalutamide, but not with cyproterone acetate. 'Hepatitis' and 'cholestatic hepatitis' were the most frequent terms coded. In 38% of the reports related to cyproterone acetate, 18% of those related to flutamide and 33% of those related to bicalutamide the patient had simultaneously received other hepatotoxic drugs. The disproportionality analysis of hepatitis showed a strong association with flutamide and a weak association with bicalutamide and cyproterone acetate. Mean doses of flutamide and bicalutamide were very close to their defined daily dose (DDD) to treat prostate cancer, although in the case of cyproterone acetate it was slightly higher. The latency period of hepatitis was between 3 and 10 months for the three antiandrogens, and the recovery period was shorter (0.5-3 months). The majority of the reported cases of hepatitis evolved favourably.
Our results highlight the hepatotoxic potential of flutamide compared to cyproterone acetate. The data related to bicalutamide should be cautiously considered due to the smaller number of reports.
分析医生、药剂师和护士自发报告的甾体类和非甾体类抗雄激素药物所致肝毒性的类型及主要特征。该分析可增加有关这些不良反应的信息,目前这些信息主要来自已发表的个别病例。
利用西班牙药物警戒数据库,检索自每种抗雄激素药物获批之日起至当前记录的自发报告。我们分析了肝脏疾病的发生频率、编码的首选术语、其他肝毒性药物的存在情况以及肝炎病例的特征。
肝脏疾病是与氟他胺和比卡鲁胺相关的最常见不良反应,但与醋酸环丙孕酮无关。“肝炎”和“胆汁淤积性肝炎”是最常编码的术语。在与醋酸环丙孕酮相关的报告中,38%;与氟他胺相关的报告中,18%;与比卡鲁胺相关的报告中,33%的患者同时接受了其他肝毒性药物。肝炎的不成比例分析显示,与氟他胺有很强的关联,与比卡鲁胺和醋酸环丙孕酮有较弱的关联。氟他胺和比卡鲁胺的平均剂量非常接近其治疗前列腺癌的规定日剂量(DDD),不过醋酸环丙孕酮的剂量略高。三种抗雄激素药物所致肝炎的潜伏期为3至10个月,恢复期较短(0.5至3个月)。大多数报告的肝炎病例病情好转。
我们的结果突出了氟他胺相较于醋酸环丙孕酮的肝毒性潜力。由于报告数量较少,与比卡鲁胺相关的数据应谨慎考虑。