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Predicting High-Grade Cancer at Ten-Core Prostate Biopsy Using Four Kallikrein Markers Measured in Blood in the ProtecT Study

Lookup NU author(s): Dr Mary Robinson

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This work is licensed under a Creative Commons Attribution 4.0 International License (CC BY 4.0).


Abstract

Background: Many men with elevated prostate-specific antigen (PSA) levels in serum do not have aggressive prostate cancer and undergo unnecessary biopsy. Retrospective studies using cryopreserved serum suggest that four kallikrein markers can predict biopsy outcome.Methods: Free, intact and total PSA, and kallikrein-related peptidase 2 were measured in cryopreserved blood from 6129 men with elevated PSA (>= 3.0 ng/mL) participating in the prospective, randomized trial Prostate Testing for Cancer and Treatment. Marker levels from 4765 men providing anticoagulated plasma were incorporated into statistical models to predict any-grade and high-grade (Gleason score >= 7) prostate cancer at 10-core biopsy. The models were corrected for optimism by 10-fold cross validation and independently validated using markers measured in serum from 1364 men. All statistical tests were two-sided.Results: The four kallikreins enhanced prostate cancer detection compared with PSA and age alone. Area under the curve (AUC) for the four kallikreins was 0.719 (95% confidence interval [CI] = 0.704 to 0.734) vs 0.634 (95% CI = 0.617 to 0.651, P < .001) for PSA and age alone for any-grade cancer, and 0.820 (95% CI = 0.802 to 0.838) vs 0.738 (95% CI = 0.716 to 0.761) for high-grade cancer. Using a 6% risk of high-grade cancer as an illustrative cutoff, for 1000 biopsied men with PSA levels of 3.0 ng/mL or higher, the model would reduce the need for biopsy in 428 men, detect 119 high-grade cancers, and delay diagnosis of 14 of 133 high-grade cancers. Models exhibited excellent discrimination on independent validation among men with only serum samples available for analysis.Conclusions: A statistical model based on kallikrein markers was validated in a large prospective study and reduces unnecessary biopsies while delaying diagnosis of high-grade cancers in few men.


Publication metadata

Author(s): Bryant RJ, Sjoberg DD, Vickers AJ, Robinson MC, Kumar R, Marsden L, Davis M, Scardino PT, Donovan J, Neal DE, Lilja H, Hamdy FC

Publication type: Article

Publication status: Published

Journal: JNCI-Journal of the National Cancer Institute

Year: 2015

Volume: 107

Issue: 7

Pages: 1-7

Print publication date: 01/07/2015

Online publication date: 11/04/2015

Acceptance date: 11/03/2015

Date deposited: 20/05/2016

ISSN (print): 0027-8874

ISSN (electronic): 1460-2105

Publisher: Oxford University Press

URL: http://dx.doi.org/10.1093/jnci/djv095

DOI: 10.1093/jnci/djv095


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Funding

Funder referenceFunder name
Cancer Research UK Oxford Centre
National Institute for Health Research (NIHR) Oxford Biomedical Research Centre Program
David H. Koch through the Prostate Cancer Foundation
FiDIPro-program award from TEKES
Fundacion Federico SA
Sidney Kimmel Center for Prostate and Urologic Cancers
11-0624Swedish Cancer Society
96/20/99UK National Institute for Health Research Health Technology Programme
P50 CA092629National Cancer Institute at the National Institutes of Health
R01 CA160816National Cancer Institute at the National Institutes of Health
R01 CA175491National Cancer Institute at the National Institutes of Health

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