Liang Yuanyuan, Ketchum Norma S, Louden Christopher, Jimenez-Rios Miguel A, Thompson Ian M, Camarena-Reynoso Hector R
Department of Epidemiology and Biostatistics, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA. liangy @ uthscsa.edu
Urol Int. 2012;89(1):9-16. doi: 10.1159/000338270. Epub 2012 May 24.
To perform the first validation study of the finasteride-adjusted Prostate Cancer Prevention Trial Prostate Cancer Risk Calculator (finPCPTRC) in a contemporary referral population in Mexico.
837 patients referred to the Instituto Nacional de Cancerología, Mexico City, Mexico, between 2005 and 2009 were used to validate the finPCPTRC by examining various measures of discrimination and calibration. Net benefit curve analysis was used to gain insight into the use of the finPCPTRC for clinical decisions.
Prostate cancer (PCa) incidence (72.8%) was high in this Mexican referral cohort and 45.7% of men who were diagnosed with PCa had high-grade lesions (HGPCa, Gleason score >6). 1.3% of the patients were taking finasteride. The finPCPTRC was a superior diagnostic tool compared to prostate-specific antigen alone when discriminating patients with PCa from those without PCa (AUC = 0.784 vs. AUC = 0.687, p < 0.001) and when discriminating patients with HGPCa from those without HGPCa (AUC = 0.768 vs. AUC = 0.739, p < 0.001). The finPCPTRC underestimated the risk of PCa but overestimated the risk of HGPCa (both p < 0.001). Compared with other strategies to opt for biopsy, the net benefit would be larger with utilization of the finPCPTRC for patients accepting higher risks of HGPCa.
Rates of biopsy-detectable PCa and HGPCa were high and 1.3% of this referral cohort in Mexico was taking finasteride. The risks of PCa or HGPCa calculated by the finPCPTRC were not well calibrated for this referral Mexican population and new clinical diagnostic tools are needed.
在墨西哥当代转诊人群中对非那雄胺调整后的前列腺癌预防试验前列腺癌风险计算器(finPCPTRC)进行首次验证研究。
2005年至2009年间转诊至墨西哥城墨西哥国立癌症研究所的837例患者,通过检查各种区分度和校准指标来验证finPCPTRC。采用净效益曲线分析来深入了解finPCPTRC在临床决策中的应用。
该墨西哥转诊队列中前列腺癌(PCa)发病率较高(72.8%),45.7%被诊断为PCa的男性患有高级别病变(HGPCa,Gleason评分>6)。1.3%的患者正在服用非那雄胺。在区分PCa患者与非PCa患者时(AUC = 0.784 vs. AUC = 0.687, p < 0.001)以及区分HGPCa患者与非HGPCa患者时(AUC = 0.768 vs. AUC = 0.739, p < 0.001),与单独使用前列腺特异性抗原相比,finPCPTRC是一种更优的诊断工具。finPCPTRC低估了PCa风险,但高估了HGPCa风险(均p < 0.001)。与其他选择活检的策略相比,对于接受较高HGPCa风险的患者,使用finPCPTRC的净效益会更大。
活检可检测到的PCa和HGPCa发生率较高,该墨西哥转诊队列中有1.3%的患者正在服用非那雄胺。对于该墨西哥转诊人群,finPCPTRC计算出的PCa或HGPCa风险校准不佳,需要新的临床诊断工具。