Rabe T, Feldmann K, Heinemann L, Runnebaum B
Gynaecological Endocrinology and Reproductive Medicine, University Women's Hospital Heidelberg, Germany.
Drug Saf. 1996 Jan;14(1):25-38. doi: 10.2165/00002018-199614010-00004.
The preclinical safety assessment of cyproterone acetate (CPA) with regard to liver tumorigenesis was based on tumorigenicity studies, which revealed no mutagenic potential. Recently, in vitro studies on the formation of adducts and the enhancement of DNA repair synthesis with CPA have been published. These results are not unique to CPA, and the role of adducts and increased DNA synthesis in mutagenesis is still not clear. Dose-related hepatic toxicity has been reported with the prolonged use of CPA. An active surveillance study of patients taking long term CPA treatment has shown no correlation between the duration of CPA treatment and the prevalence of liver enzyme elevations. In a multicentre surveillance study of long term CPA use in 2506 patients included so far, not a single case of hepatocellular carcinoma has been observed. These findings do not support the theory of an elevated risk of hepatocellular carcinoma as a result of CPA treatment. In conclusion, there have been no observations which could point to an increased risk of proliferative liver change as a result of CPA treatment.
醋酸环丙孕酮(CPA)关于肝脏肿瘤发生的临床前安全性评估基于致癌性研究,该研究表明其无致突变潜力。最近,已发表了关于CPA加合物形成及DNA修复合成增强的体外研究。这些结果并非CPA所特有,且加合物和DNA合成增加在诱变中的作用仍不清楚。有报道称长期使用CPA会出现剂量相关的肝毒性。一项对长期接受CPA治疗患者的主动监测研究表明,CPA治疗持续时间与肝酶升高患病率之间无相关性。在迄今为止纳入2506例患者的长期使用CPA的多中心监测研究中,未观察到一例肝细胞癌病例。这些发现不支持CPA治疗会导致肝细胞癌风险升高的理论。总之,没有观察结果表明CPA治疗会增加增殖性肝脏改变的风险。