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非那雄胺对前列腺特异性抗原水平的长期影响:前列腺癌预防试验的结果

Long-term effects of finasteride on prostate specific antigen levels: results from the prostate cancer prevention trial.

作者信息

Etzioni Ruth D, Howlader Nadia, Shaw Pamela A, Ankerst Donna P, Penson David F, Goodman Phyllis J, Thompson Ian M

机构信息

Fred Hutchinson Cancer Research Center, Seattle, Washington 98109-1024, USA.

出版信息

J Urol. 2005 Sep;174(3):877-81. doi: 10.1097/01.ju.0000169255.64518.fb.

DOI:10.1097/01.ju.0000169255.64518.fb
PMID:16093979
Abstract

PURPOSE

Studies have shown that finasteride decreases prostate specific antigen (PSA) by approximately 50% during the first 12 months of use. We estimated the long-term effects of finasteride on PSA in men with and without a prostate cancer diagnosis at the end of the study.

MATERIALS AND METHODS

We analyzed serial PSA in participants in the Prostate Cancer Prevention Trial who had an end of study biopsy (928 with cancer and 8,620 with negative biopsy) or an interim diagnosis of prostate cancer (671). Linear mixed effects regression models were fit to longitudinal PSA values beginning 1 year after randomization.

RESULTS

In subjects with no cancer in the end of study biopsy PSA in the finasteride arm showed a median annual decrease of 2% [corrected] after year 1, while PSA in the control arm showed an annual increase of 3% (p <0.001). In end of study cases PSA increased annually by 6% (placebo) and 7% (finasteride). In those with interim diagnoses PSA increased by 11% (placebo) and 15% (finasteride) each year prior to diagnosis. Cases with high grade disease (Gleason 7 and above) had greater PSA increases than cases with low grade disease (p <0.001).

CONCLUSIONS

In men who have been receiving finasteride for more than 1 year time varying adjustment factors may be needed to determine whether PSA is in the normal range. In the Prostate Cancer Prevention Trial cohort the adjustment factor required to preserve median PSA increased from 2 at 24 months to 2.5 at 7 years after the initiation of finasteride.

摘要

目的

研究表明,非那雄胺在使用的前12个月可使前列腺特异性抗原(PSA)降低约50%。我们评估了非那雄胺对研究结束时已诊断和未诊断前列腺癌男性PSA的长期影响。

材料与方法

我们分析了前列腺癌预防试验参与者的系列PSA,这些参与者在研究结束时进行了活检(928例患有癌症,8620例活检阴性)或前列腺癌的中期诊断(671例)。线性混合效应回归模型适用于随机分组1年后开始的纵向PSA值。

结果

在研究结束时活检未患癌症的受试者中,非那雄胺组的PSA在第1年后每年中位数下降2%[校正后],而对照组的PSA每年上升3%(p<0.001)。在研究结束时的病例中,PSA每年上升6%(安慰剂组)和7%(非那雄胺组)。在中期诊断的患者中,在诊断前PSA每年上升11%(安慰剂组)和15%(非那雄胺组)。高级别疾病(Gleason 7及以上)的病例比低级别疾病的病例PSA升高幅度更大(p<0.001)。

结论

对于接受非那雄胺治疗超过1年的男性,可能需要采用随时间变化的调整因素来确定PSA是否在正常范围内。在前列腺癌预防试验队列中,维持PSA中位数所需的调整因素从非那雄胺开始使用后24个月时的2增加到7年时的2.5。

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