A Prospective, Multicenter, National Cancer Institute Early Detection Research Network Study of [-2]proPSA: Improving Prostate Cancer Detection and Correlating with Cancer Aggressiveness

被引:163
作者
Sokoll, Lori J. [1 ,2 ]
Sanda, Martin G. [3 ]
Feng, Ziding [4 ]
Kagan, Jacob [5 ]
Mizrahi, Isaac A. [6 ]
Broyles, Dennis L. [6 ]
Partin, Alan W. [1 ,2 ]
Srivastava, Sudhir [5 ]
Thompson, Ian M. [7 ]
Wei, John T. [8 ]
Zhang, Zhen [1 ,2 ]
Chan, Daniel W. [1 ,2 ]
机构
[1] Johns Hopkins Med Inst, Dept Pathol, Baltimore, MD 21287 USA
[2] Johns Hopkins Med Inst, Dept Urol, Baltimore, MD 21287 USA
[3] Beth Israel Deaconess Med Ctr, Div Urol, Boston, MA 02215 USA
[4] Fred Hutchinson Canc Res Ctr, Div Publ Hlth Sci, Seattle, WA 98104 USA
[5] NCI, Canc Prevent Div, Canc Biomarkers Res Grp, Rockville, MD USA
[6] Beckman Coulter Inc, San Diego, CA USA
[7] Univ Texas Hlth Sci Ctr San Antonio, Dept Urol, San Antonio, TX 78229 USA
[8] Univ Michigan, Dept Urol, Ann Arbor, MI 48109 USA
关键词
PROPROSTATE-SPECIFIC ANTIGEN; ARTIFICIAL NEURAL-NETWORK; PRECURSOR FORM; BENIGN PSA; SERUM; MEN; NG/ML; DIFFERENTIATION; BIOMARKERS; COMPLEX;
D O I
10.1158/1055-9965.EPI-10-0007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The free prostate-specific antigen (PSA) isoform, [-2]proPSA, has been shown to be associated with prostate cancer. The study objective was to characterize the clinical utility of serum [-2]proPSA for prostate cancer detection and assess its association with aggressive disease. Methods: From among 669 subjects in a prospective prostate cancer detection study at four National Cancer Institute Early Detection Research Network clinical validation centers, 566 were eligible. Serum PSA, free PSA, and [-2]proPSA were measured (Beckman Coulter Access 2 Analyzer). Results: Two hundred and forty-five (43%) of the 566 participants had prostate cancer on biopsy. At 70% specificity, the sensitivity of %[-2]proPSA ([-2]proPSA/fPSA) was 54% [95% confidence interval (CI), 48-61%; null hypothesis, 40%]. Including %[-2]proPSA in a multivariate prediction model incorporating PSA and % fPSA improved the performance (P < 0.01). In the 2 to 4 ng/mL PSA range, %[-2]proPSA outperformed % fPSA (receiver operator characteristic-areas under the curve, 0.73 versus 0.61; P = 0.01). At 80% sensitivity, %[-2]proPSA had significantly higher specificity (51.6%; 95% CI, 41.2-61.8%) than PSA (29.9%; 95% CI, 21.040.0%) and % fPSA (28.9%; 95% CI, 20.1-39.0%). In the 2 to 10 ng/mL PSA range, a multivariate model had significant improvement (area under the curve, 0.76) over individual PSA forms (P < 0.01 to < 0.0001). At 80% sensitivity, the specificity of %[-2]proPSA (44.9%; 95% CI, 38.4-51.5%) was significantly higher than PSA (30.8%; 95% CI, 24.9-37.1%) and relatively higher than % fPSA (34.6%; 95% CI, 28.5-41.4%). %[-2]proPSA increased with increasing Gleason score (P < 0.001) and was higher in aggressive cancers (P = 0.03). Conclusions: In this prospective study, %[-2]proPSA showed potential clinical utility for improving prostate cancer detection and was related to the risk of aggressive disease. Impact: The addition of %[-2]proPSA could affect the early detection of prostate cancer. Cancer Epidemiol Biomarkers Prev; 19(5); 1193-200. (C)2010 AACR.
引用
收藏
页码:1193 / 1200
页数:8
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