Association of prostate-specific antigen doubling time and cancer in men undergoing repeat prostate biopsy

作者：Moreira Daniel M^*; Gerber Leah; Thomas Jean Alfred; Banez Lionel L; McKeever Madeline G; Freedland Stephen J

来源：International Journal of Urology, 2012, 19(8): 741-747.

DOI：10.1111/j.1442-2042.2012.03016.x

• biopsy
• diagnosis
• kinetics
• pathology
• prostate-specific antigen
• prostatic neoplasm

Objectives: To analyze the association between prostate-specific antigen doubling time with prostate cancer risk and grade among men with prostate-specific antigen levels =4.0 ng/mL undergoing repeat prostate biopsy. Methods: A total of 286 patients with prostate-specific antigen =4 ng/mL and available prostate-specific antigen doubling time data, who underwent repeat prostate biopsy from 19962009, were included in this analysis. Prostate-specific antigen doubling time was divided into three groups: >9 years, 39 years and <3 years. Multivariate analyses of prostate-specific antigen doubling time with cancer risk and grade (=3 + 4 vs=4 + 3) were carried out using logistic regression adjusting for prebiopsy prostate-specific antigen, race, age, digital rectal examination, year of biopsy and number of prior negative biopsies. Results: The median prostate-specific antigen doubling time before biopsy was 4.5 years (interquartile range = 2.510). Shorter prostate-specific antigen doubling time was associated with higher prostate-specific antigen (P < 0.001), but it was unrelated to age, digital rectal examination or race. Shorter prostate-specific antigen doubling time as a continuous variable was associated with greater prostate cancer risk in both uni- (hazard ratio = 0.99, 95% confidence interval = 0.980.99, P = 0.001) and multivariate analysis (hazard ratio = 0.99, 95% confidence interval = 0.980.99, P = 0.004). The prevalence of cancer among prostate-specific antigen doubling time groups (>9, 39, <3 years) was 17%, 37% and 40%, respectively. Shorter prostate-specific antigen doubling time groups were associated with higher cancer risk (P = 0.001). Stratified by grade, short prostate-specific antigen doubling time as a continuous variable significantly predicted both low- (P = 0.010) and high-grade disease (P = 0.049). The inclusion of prostate-specific antigen doubling time groups in a multivariate model to predict biopsy positivity increased its accuracy from 0.69 to 0.74. Conclusion: Prostate-specific antigen doubling time seems to provide further cancer risk assessment in men undergoing repeat biopsy for prostate-specific antigen =4.0 ng/mL. If validated in future studies, the present findings support the use of prostate-specific antigen doubling time in the risk stratification of this patient population.

• 出版日期2012-8