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. 2004 Spring;6(2):58–72.

Table 2.

Clinical Performance of Selected, Promising Serologic Prostate Cancer Biomarkers

Aid to
Diagnosis/ Pathologic Predicting Distant Follow-up/ Selection for
Future Case- Staging/ PSA Metastasis Monitoring Targeted
Biomarker Risk Screening Finding Prognosis* Recurrence Staging Therapy Therapy
PSA Yes Yes Yes Yes Yes Yes Yes Yes
Free PSA - No Yes Yes No No No -
Complexed PSA - No Yes Yes No No - -
hK2 - - Yes Yes - - - -
BPSA - No - - - - - -
ProPSA - No Yes Yes - - - -
isoforms
IGF-I Yes No No No No No No -
IGFBP-2 - - Yes Yes; not Yes No No Yes
lymph nodes
IGFBP-3 Controversial No No No Yes Yes No Yes
TGF-β1 - No No Yes Yes Yes Yes Yes
IL-6 - No No Only Yes Yes No Yes
lymph nodes
IL-6sR - No No Only Yes Yes No Yes
lymph nodes
uPA - No Yes Yes; not Yes Yes - -
lymph nodes
uPAR - No Yes Yes; not Yes Yes - -
lymph nodes
VEGF - No Yes Yes Yes Yes - -
Osteoprotegerin - No No - - Yes - -
RT-PCR/PSA - No No No No No Yes -
RT-PCR/hK2 - No No Yes Yes No - -
*

Including metastases to regional pelvic lymph nodes.

In experimental prostate cancer models; no published results from phase 3 human clinical trials.

No, not useful; Yes, useful; –, application is not considered and/or association has not been investigated; PSA, prostate-specific antigen; hK2, human glandular kallikrein 2; BPSA, “benign” PSA; IGF, insulin-like growth factor; IGFBP, insulin-like growth factor binding protein; TGF-β1, transforming growth factor β1; IL-6, interleukin-6; IL-6sR, interleukin-6 soluble receptor; uPA, urokinase plasminogen activator; uPAR, urokinase plasminogen activator receptor; VEGF, vascular endothelial growth factor; RT-PCR, reverse transcriptase polymerase chain reaction.