deVere White Ralph W, Hackman Robert M, Soares Stephanie E, Beckett Laurel A, Li Yueju, Sun Buxiang
Department of Urology, University of California, Davis, School of Medicine, Sacramento, California 95817, USA.
Urology. 2004 Feb;63(2):259-63. doi: 10.1016/j.urology.2003.09.061.
To determine whether supplemental amounts of soy isoflavone (genistein-rich extract) would lower prostate-specific antigen (PSA) levels more than 50% in patients with prostate cancer (CaP).
A total of 62 men (mean age 73.6 years, range 61.4 to 89.3) with histologically proven CaP who had two consecutive elevated PSA readings were accrued during a 13-month period. An open-label pilot study was conducted for 6 months in which the patients took capsules containing the genistein-rich extract three times daily by mouth. The subjects were in one of five groups: after radical retropubic prostatectomy (n = 9), after radiotherapy (n = 17), after both radical retropubic prostatectomy and radiotherapy (n = 6), off-cycle during hormonal therapy (intermittent hormones; n = 14), or active surveillance (n = 16). The primary endpoint for the trial was a 50% reduction in the PSA level at 6 months compared with before treatment.
Of the 62 men enrolled, 52 were available for evaluation at 6 months. Three patients discontinued because of adverse events (diarrhea) and seven because of personal choice. One of 52 patients had a more than 50% reduction in the PSA level (1.9% response, 95% confidence interval 0.1% to 10.3%). An additional 7 patients had PSA reductions that were less than 50%. All 8 patients with lower PSA levels at 6 months were in the active surveillance (watchful waiting) treatment subgroup. Repeated measure regression models allowing for correlation between initial levels and change also indicated a decline in PSA in this group compared with other groups: 0 of 52 had a complete response, 9 (17%) had a partial response, 8 (15%) had stable disease, and 35 (67%) had disease progression. In the 9 patients with a partial response, 6 had pathologic findings that were moderately differentiated, 2 had well-differentiated findings, and 1 had poorly differentiated findings. Therefore, the response in this group of patients did not appear to be driven by the Gleason score. The total testosterone level was lowered in one of the patients responding, but it was higher in five others.
A genistein-rich extract as the sole treatment for CaP did not reduce PSA levels by 50% or more in 51 of 52 subjects. Thus, it does not appear to be an effective treatment for CaP when given alone. However, 8 of 13 evaluated patients in the active surveillance group had either no rise or a decline in PSA levels of less than 50%. More study is warranted for those choosing active surveillance.
确定补充大豆异黄酮(富含染料木黄酮的提取物)是否比前列腺癌(CaP)患者中降低前列腺特异性抗原(PSA)水平超过50%。
在13个月期间,共纳入62名经组织学证实患有CaP且连续两次PSA读数升高的男性(平均年龄73.6岁,范围61.4至89.3岁)。进行了一项为期6个月的开放标签试点研究,患者每天口服三次含有富含染料木黄酮提取物的胶囊。受试者分为五组之一:根治性耻骨后前列腺切除术后(n = 9)、放疗后(n = 17)、根治性耻骨后前列腺切除术和放疗后(n = 6)、激素治疗周期外(间歇性激素;n = 14)或积极监测(n = 16)。该试验的主要终点是与治疗前相比,6个月时PSA水平降低50%。
在纳入的62名男性中,52名在6个月时可进行评估。3名患者因不良事件(腹泻)停药,7名因个人选择停药。52名患者中有1名PSA水平降低超过50%(1.9%的缓解率,95%置信区间0.1%至10.3%)。另外7名患者的PSA降低幅度小于50%。6个月时PSA水平较低的所有8名患者均在积极监测(密切观察等待)治疗亚组中。考虑到初始水平和变化之间相关性的重复测量回归模型也表明,与其他组相比,该组PSA下降:52名患者中0名完全缓解,9名(17%)部分缓解,8名(15%)疾病稳定,35名(67%)疾病进展。在9名部分缓解的患者中,6名有中度分化的病理结果,2名有高分化结果,1名有低分化结果。因此,该组患者的反应似乎不是由Gleason评分驱动的。1名有反应患者的总睾酮水平降低,但另外5名患者的总睾酮水平升高。
富含染料木黄酮的提取物作为CaP的唯一治疗方法,在52名受试者中的51名中未使PSA水平降低50%或更多。因此,单独使用时似乎不是CaP的有效治疗方法。然而,积极监测组中13名接受评估的患者中有8名PSA水平要么没有升高,要么降低幅度小于50%。对于选择积极监测的患者,有必要进行更多研究。