Yang X J, Lecksell K, Short K, Gottesman J, Peterson L, Bannow J, Schellhammer P F, Fitch W P, Hodge G B, Parra R, Rouse S, Waldstreicher J, Epstein J I
Department of Pathology, University of Chicago Medical Center, Illinois, USA.
Urology. 1999 Apr;53(4):696-700. doi: 10.1016/s0090-4295(98)00579-2.
Finasteride, a common agent used to treat benign prostatic hyperplasia (BPH), inhibits 5-alpha-reductase. Testosterone is converted by 5-alpha-reductase to the more potent dihydrotestosterone, which is the primary androgen in the prostate. Leuprolide is a stronger antiandrogen that is used to downstage prostate cancer before radical prostatectomy. Leuprolide induces marked atrophy of prostate carcinoma cells, which sometimes makes pathologic diagnosis of cancer difficult, although evaluation at radical prostatectomy is easier than at biopsy. It is unknown whether finasteride produces similar changes, which would result in greater diagnostic difficulty because such changes would be seen on biopsy to rule out cancer in men with suspicious clinical findings treated for BPH. The current study investigated the histologic effects of finasteride therapy on human prostate cancer and benign prostatic tissue on needle biopsy.
In blinded manner, we reviewed 53 needle biopsy specimens showing prostate carcinoma (35 treated with finasteride, 18 with placebo). Also reviewed in blinded manner were 50 benign needle biopsy specimens (25 treated with finasteride, 25 with placebo). The Gleason score, number of cores involved, percentage cancer involvement in a core, percentage of atrophic changes in cancer cells, presence of mitoses, blue-tinged mucinous secretions, prominent nucleoli, and high-grade prostatic intraepithelial neoplasia were documented for each case in the cancer group. The percentage of atrophy, basal cell hyperplasia, transitional metaplasia, chronic inflammation, and stromal proliferation was documented for each case in the benign group.
No significant histologic differences were present in either the benign or cancer group between cases treated with finasteride and placebo.
We conclude that finasteride treatment for BPH does not cause difficulty in the diagnosis of cancer in prostate needle specimens. It is possible that there are severely atrophic areas resulting from finasteride treatment that are undersampled. However, the conclusion that cancer seen on needle biopsy in men treated with finasteride is unaltered and readily identified as cancer remains valid.
非那雄胺是一种用于治疗良性前列腺增生(BPH)的常用药物,可抑制5α-还原酶。睾酮经5α-还原酶转化为活性更强的双氢睾酮,而双氢睾酮是前列腺中的主要雄激素。亮丙瑞林是一种更强效的抗雄激素药物,用于在根治性前列腺切除术前行前列腺癌降期治疗。亮丙瑞林可导致前列腺癌细胞显著萎缩,这有时会使癌症的病理诊断变得困难,不过在根治性前列腺切除术中进行评估比在活检时更容易。尚不清楚非那雄胺是否会产生类似变化,而这会导致更大的诊断困难,因为在对有可疑临床症状接受BPH治疗的男性进行活检以排除癌症时会出现此类变化。本研究调查了非那雄胺治疗对人前列腺癌及针吸活检时良性前列腺组织的组织学影响。
我们以盲法回顾了53份显示前列腺癌的针吸活检标本(35例接受非那雄胺治疗,18例接受安慰剂治疗)。还以盲法回顾了50份良性针吸活检标本(25例接受非那雄胺治疗,25例接受安慰剂治疗)。记录癌症组中每例患者的Gleason评分、受累核心数量、核心中癌组织所占百分比、癌细胞萎缩变化百分比、有丝分裂情况、蓝色黏液样分泌物、显著核仁以及高级别前列腺上皮内瘤变。记录良性组中每例患者的萎缩百分比、基底细胞增生、移行化生、慢性炎症以及间质增生情况。
在接受非那雄胺治疗和安慰剂治疗的病例中,良性组和癌症组均未出现显著的组织学差异。
我们得出结论,非那雄胺治疗BPH不会导致前列腺针吸标本中癌症诊断困难。有可能非那雄胺治疗导致的严重萎缩区域取样不足。然而,在用非那雄胺治疗的男性针吸活检中所见癌症未发生改变且易于识别为癌症这一结论仍然成立。