Thompson Ian M, Tangen Catherine M, Parnes Howard L, Lippman Scott M, Coltman Charles A
Department of Urology, University of Texas Health Science Center at San Antonio, San Antonio, Texas 78229, USA.
Urology. 2008 May;71(5):854-7. doi: 10.1016/j.urology.2008.01.025.
Finasteride reduced the risk of prostate cancer by 24.8% in the Prostate Cancer Prevention Trial (PCPT). Whether this represents treatment or prevention and who is most likely to benefit are unknown. We sought to clarify these issues by this investigation.
We fit a logistic regression model to men in the placebo group of the PCPT using risk factors for prostate cancer at entry to predict prostate cancer during the subsequent 7 years of study. Men in the two treatment groups were categorized into quintiles of risk of prostate cancer based on the predictive logistic model. A second model was fit evaluating finasteride's effect on prostate cancer for each subgroup defined by quartiles of baseline prostate-specific antigen (PSA) . The magnitude of the prevention effect of finasteride on prostate cancer was then evaluated across risk and PSA strata.
Finasteride significantly reduced prostate cancer risk for all risk quintiles. For quintiles 1 through 5, odds ratios were 0.72, 0.52, 0.64, 0.66, and 0.71, respectively (all P < or = 0.05). For quartiles of risk of entry PSA (less than 0.7 ng/mL, 0.7 to 1.1 ng/mL, 1.1 to 1.7 ng/mL, and 1.8 to 3.0 ng/mL), odds ratios increased (smaller treatment effect) as PSA increased: 0.60, 0.62, 0.66, and 0.69, respectively, but remained significant for all strata (each P < 0.001).
Finasteride significantly reduced prostate cancer risk regardless of the level of this risk, estimated either by multivariable risk or by PSA stratum; this suggests that finasteride exerts both treatment and preventive effects. All men undergoing PSA screening should be informed of the potential for finasteride to reduce their risk of prostate cancer.
在前列腺癌预防试验(PCPT)中,非那雄胺使前列腺癌风险降低了24.8%。这是代表治疗作用还是预防作用,以及谁最有可能从中受益尚不清楚。我们试图通过这项研究来阐明这些问题。
我们对PCPT安慰剂组的男性患者建立了一个逻辑回归模型,使用入组时的前列腺癌风险因素来预测随后7年研究期间的前列腺癌。根据预测逻辑模型,将两个治疗组的男性患者分为前列腺癌风险五分位数组。针对由基线前列腺特异性抗原(PSA)四分位数定义的每个亚组,建立了第二个模型来评估非那雄胺对前列腺癌的影响。然后在风险和PSA分层中评估非那雄胺对前列腺癌的预防作用大小。
非那雄胺显著降低了所有风险五分位数组的前列腺癌风险。对于第1至5五分位数组,比值比分别为0.72、0.52、0.64、0.66和0.71(所有P≤0.05)。对于入组PSA风险的四分位数组(小于0.7 ng/mL、0.7至1.1 ng/mL、1.1至1.7 ng/mL和1.8至3.0 ng/mL),随着PSA升高,比值比增加(治疗效果较小):分别为0.60、0.62、0.66和0.69,但在所有分层中均保持显著(每个P<0.001)。
无论通过多变量风险还是PSA分层估计的风险水平如何,非那雄胺均显著降低前列腺癌风险;这表明非那雄胺具有治疗和预防作用。所有接受PSA筛查的男性都应被告知非那雄胺降低其前列腺癌风险的可能性。