Andriole Gerald, Bostwick David, Civantos Francisco, Epstein Jonathan, Lucia M Scott, McConnell John, Roehrborn Claus G
Division of Urologic Surgery, School of Medicine, Washington University-St. Louis, 4960 Children's Place, St. Louis, MO 63110, USA.
J Urol. 2005 Dec;174(6):2098-104. doi: 10.1097/01.ju.0000181216.71605.38.
The Prostate Cancer Prevention Trial (PCPT) showed that the 5alpha-reductase inhibitor (5ARI) finasteride significantly decreased the 7-year period prevalence of prostate cancer vs placebo. However, Gleason score 7-10 tumors were significantly more common in the finasteride vs the placebo group. We considered data on the effects of 5ARIs on prostate cancer natural history and detection.
A detailed review was performed of the literature identified from the MEDLINE database examining the effects of 5ARIs on prostate cancer prevalence and tumor histopathology.
In PCPT there were fewer biopsies performed for cause in the finasteride vs the placebo group and the proportion of high grade tumors in the treatment groups did not diverge with time. Given that finasteride has an effect on prostate specific antigen and prostate volume, which are key factors in triggering prostate biopsies, they may be significant confounders of Gleason score results. Prostate shrinkage in the finasteride treated group may minimize biopsy sampling error. Furthermore, histological studies have shown that 5ARIs have a significant effect on prostate architecture, which can make the interpretation of prostate specimens in men treated with 5ARIs difficult. Further evaluation of PCPT findings will help determine the true nature of these observations.
5ARIs decrease the risk of prostate cancer but also alter the detection of disease through effects on prostate specific antigen, and prostate volume and histology. The weight of evidence suggests an artifactual effect of finasteride on Gleason grading in the PCPT. The role of 5ARIs for prostate cancer chemoprevention needs further examination before it can be considered for wide recommendation.
前列腺癌预防试验(PCPT)表明,与安慰剂相比,5α还原酶抑制剂(5ARI)非那雄胺显著降低了前列腺癌7年的患病期患病率。然而,在非那雄胺组中,Gleason评分为7 - 10分的肿瘤比安慰剂组更为常见。我们研究了5ARI对前列腺癌自然病程及检测影响的数据。
对从MEDLINE数据库中检索到的文献进行详细综述,这些文献探讨了5ARI对前列腺癌患病率及肿瘤组织病理学的影响。
在PCPT中,非那雄胺组因病因进行的活检比安慰剂组少,且治疗组中高级别肿瘤的比例并未随时间而出现差异。鉴于非那雄胺对前列腺特异性抗原和前列腺体积有影响,而这两者是触发前列腺活检的关键因素,它们可能是Gleason评分结果的重要混杂因素。非那雄胺治疗组中前列腺缩小可能会将活检采样误差降至最低。此外,组织学研究表明,5ARI对前列腺结构有显著影响,这可能会使对接受5ARI治疗男性的前列腺标本解读变得困难。对PCPT研究结果的进一步评估将有助于确定这些观察结果的真实性质。
5ARI降低了前列腺癌风险,但也通过对前列腺特异性抗原、前列腺体积和组织学的影响改变了疾病的检测。现有证据表明,非那雄胺在PCPT中对Gleason分级存在人为影响。在5ARI被广泛推荐用于前列腺癌化学预防之前,其作用需要进一步研究。