Prostate-specific antigen density (PSAD) is a clinical parameter with diagnostic
value in urology. Normalizing PSA concentrations to prostatic volume enables
PSAD assessment, providing information beyond that obtainable with total PSA
alone, thereby improving specificity and decreasing unnecessary biopsies. The
value of 0.15–0.20 ng/mL/cm³ is widely used to limit the risk of significant cancers
while avoiding the pitfalls of over-detection. The use of PSAD is considered to have
specific diagnostic utility in cases with ambiguous multiparametric magnetic
resonance imaging (mpMRI) results, particularly for lesions classified as Pi-RADS
score 3. In these conditions, it has repeatedly been shown that imaging may not be
sufficient for distinguishing between incurable and clinically relevant prostate
cancers. Precise prostate volume measurement is critical because the technique
used, such as MRI, transrectal ultrasound (TRUS), or transabdominal ultrasound
(TAUS), affects the level of accuracy in subsequent PSAD calculation. It is
imperative to note that recent developments in artificial intelligence/machine
learning may help improve the reproducibility and standardization of prostate
volume measurement. In conclusion, PSAD is an interesting and generally
applicable biomarker that improves risk assessment and, above all, biopsy decisionmaking,
especially in the assessment of the borderline prostate. However, there is
still a need for province-specific guidelines and further prospective studies
regarding the use of PSAD.
Keywords: prostate cancer (PCa); prostate-specific antigen (PSA); prostate-specific
antigen density (PSAD); multiparametric magnetic resonance imaging (mpMRI);
prostate biopsy.
