Gormley G J
Merck Research Laboratories, Rahway, NJ 07065, USA.
Semin Urol Oncol. 1996 Aug;14(3):139-44.
Finasteride, an orally active type II 5 alpha-reductase (5 alpha R) inhibitor, blocks conversion of testosterone (T) to dihydrotestosterone (DHT). The utility of finasteride in effectively managing benign prostatic hyperplasia has been documented. Use of the drug results in reduced prostate volume and serum levels. Patients receiving finasteride should be monitored with periodic digital-rectal examination (DRE) and serum PSA measurement. Patients with a sustained increase in serum PSA or an abnormal DRE require additional evaluation. There is no evidence that use of finasteride has an adverse effect on prostate cancer detection, if the drug's effect on serum PSA is recognized and accounted for.
非那雄胺是一种口服有效的II型5α-还原酶(5αR)抑制剂,可阻止睾酮(T)转化为双氢睾酮(DHT)。非那雄胺有效治疗良性前列腺增生的效用已得到证实。使用该药物可使前列腺体积和血清水平降低。接受非那雄胺治疗的患者应定期进行直肠指检(DRE)和血清前列腺特异性抗原(PSA)检测。血清PSA持续升高或DRE异常的患者需要进一步评估。如果认识到并考虑到该药物对血清PSA的影响,就没有证据表明使用非那雄胺会对前列腺癌检测产生不利影响。