Improving the evaluation and diagnosis of clinically significant prostate cancer in 2017
Current Opinion in Urology , Volume 27 - Issue 3 p. 198- 204
Purpose of review To provide an overview of the current state of the evidence and highlight recent advances in the evaluation and diagnosis of clinically significant prostate cancer, focusing on biomarkers, risk calculators and multiparametric MRI (mpMRI). Recent findings In 2017 there are numerous options to improve early detection as compared to a purely prostate-specific antigen (PSA)-based approach. All have strengths and drawbacks. In addition to repeating the PSA and performing clinical work-up (digital rectal examination and estimation of prostate volume), additional tests investigated in the initial biopsy setting are: %free PSA, Prostate Health Index, 4-kallikrein score, SelectMDx, and Michigan Prostate Score and in the repeat setting: %free PSA, Prostate Health Index, 4-kallikrein score, Prostate Cancer Antigen 3, and ConfirmMDx. Risk calculators are available for both biopsy settings and incorporate clinical data with, or without, biomarkers. mpMRI is an important diagnostic adjunct. Summary There are numerous tests available that can help increase the specificity of PSA, in the initial and repeat biopsy setting. All coincide with a small decrease in sensitivity of detecting high-grade cancer. Cost effectiveness is crucial. The way forward is a multivariable risk assessment on the basis of readily available clinical data, potentially with the addition of PSA subforms, preferably at low cost. MRI in the prediagnostic setting is promising, but is not ready for 'prime time'.
|biomarkers, biopsy, early detection, MRI, overdiagnosis, prostate cancer, risk stratification, screening|
|Current Opinion in Urology|
|Organisation||Erasmus MC: University Medical Center Rotterdam|
Carlsson, S, & Roobol-Bouts, M.J. (2017). Improving the evaluation and diagnosis of clinically significant prostate cancer in 2017. Current Opinion in Urology (Vol. 27, pp. 198–204). doi:10.1097/MOU.0000000000000382