McLeod D G
Urology Service, Walter Reed Army Medical Center, Washington, DC.
Cancer. 1993 Feb 1;71(3 Suppl):1046-9. doi: 10.1002/1097-0142(19930201)71:3+<1046::aid-cncr2820711424>3.0.co;2-m.
Prostate cancer is the most frequent cancer diagnosed in American men today. Currently, about half of all patients with newly diagnosed prostate cancer present with metastatic diseases.
Antiandrogenic drugs, or more appropriately androgen-receptor antagonists, represent a group of compounds that currently have played a limited role in the treatment of metastatic prostate cancer. Their method of action is primarily one of blocking androgens at their receptor sites in target tissues. They generally are classified as steroidal or nonsteroidal compounds. Cyproterone acetate and megestrol acetate are synthetic steroidal antiandrogenic drugs that, not only compete with testosterone and dihydrotestosterone for androgen receptors, but also have progestational activity and reduce pituitary luteinizing hormone and subsequently plasma testosterone. Nonsteroidal antiandrogenic agents (flutamide, Casodex [ICI Pharmaceuticals, England], and nilutamide) block cellular binding of androgens only, and there is no reduction of testosterone levels.
Antiandrogenics have been used in numerous trials both in Europe and the United States. This group of compounds have been used as monotherapy and in combination therapy, ie, with orchiectomy or with LHRH agonists.
Currently, antiandrogens are used primarily in conjunction with conventional medical or surgical castration to achieve maximal androgen deprivation; however, ongoing clinical studies are comparing these compounds alone against standard hormonal therapy. It seems probable that antiandrogens will play an expanding role in the treatment of metastatic prostate cancer as well as having a role in the treatment of prostate cancer.
前列腺癌是当今美国男性中最常被诊断出的癌症。目前,大约一半新诊断出的前列腺癌患者患有转移性疾病。
抗雄激素药物,或者更确切地说是雄激素受体拮抗剂,是一类目前在转移性前列腺癌治疗中作用有限的化合物。它们的作用方式主要是在靶组织的受体部位阻断雄激素。它们通常被分类为甾体或非甾体化合物。醋酸环丙孕酮和醋酸甲地孕酮是合成甾体抗雄激素药物,它们不仅与睾酮和双氢睾酮竞争雄激素受体,还具有孕激素活性,并降低垂体促黄体生成素,进而降低血浆睾酮水平。非甾体抗雄激素药物(氟他胺、康士得[英国 ICI 制药公司]和尼鲁米特)仅阻断雄激素与细胞的结合,且不会降低睾酮水平。
抗雄激素药物已在欧洲和美国进行了大量试验。这类化合物已被用作单一疗法和联合疗法,即与睾丸切除术或促性腺激素释放激素(LHRH)激动剂联合使用。
目前,抗雄激素药物主要与传统的药物或手术去势联合使用,以实现最大程度的雄激素剥夺;然而,正在进行的临床研究正在比较这些化合物单独使用与标准激素疗法的效果。抗雄激素药物似乎很可能在转移性前列腺癌的治疗中发挥越来越大的作用,并且在前列腺癌的治疗中也将发挥作用。