New study below [1].
I doubt that many in the group who know their PSA level also know their percent free PSA [%fPSA].
Some might remember their %fPSA before diagnosis. A %fPSA <25 meant that there was a high risk of PCa. With a high %fPSA, one might skip the biopsy.
However, in the setting of biochemical recurrence, a %fPSA > 15 "after RP is an indicator of a more aggressive disease. Unlike in the diagnostic setting, a higher %fPSA portends a worse clinical outcome."
Does this mean that PSA in the free form promotes progression? Why does the reverse seem to be true before diagnosis? Curious.
-Patrick
[1] pubmed.ncbi.nlm.nih.gov/320...
J Urol
, 101097JU0000000000000808 2020 Feb 18[Online ahead of print]
A High Percent-Free PSA in the Setting of Biochemical Recurrence After Radical Prostatectomy Is Associated With Poorer Outcomes: A Validation Study Using Prospectively Collected Biobank Specimens
Dixon T S Woon 1 , Jaime O Herrera-Cáceres 1 , Hanan Goldberg 1 , Hina Shiakh 1 , Emily Whelan 1 , Gregory Nason 1 , Khaled Ajib 1 , Guan Hee Tan 1 , Thenappan Chandrasekar 1 , Omar Alhunaidi 1 , Antonio Finelli 1 , Alexandre Zlotta 1 , Alejandro Berlin 1 , Eleftherios Diamantis 2 , Neil Fleshner 1
Affiliations collapse
Affiliations
1 Princess Margaret Cancer Centre, University of Toronto, Toronto, Ontario, Canada.
2 Mount Sinai Hospital, Department of Clinical Biochemistry, Toronto, Ontario, Canada.
PMID: 32068483 DOI: 10.1097/JU.0000000000000808
Abstract
Purpose: The role of percent-free PSA (%fPSA) in patients who have undergone radical prostatectomy (RP) and subsequently relapsed is unclear. We previously conducted two retrospective studies and found %fPSA ≥15 in the setting of biochemical recurrence (BCR) confers more aggressive disease. To validate that, we propose to use biobank specimens collected prospectively when patients were first diagnosed with BCR.
Materials and method: Biobank specimens of patients with undetectable PSA after RP and then develop BCR(PSA ≥0.1) were analyzed for %fPSA. Patients were stratified according to the %fPSA cut-off of 15%. Univariable and multivariable logistic regression analysis was performed to predict covariates associated with a higher %fPSA. Cox proportional hazard models were performed to evaluate the prognostic effect of %fPSA on androgen deprivation therapy (ADT) free survival, metastasis-free survival, castrate resistant (CRPC) free survival, cancer-specific (CSS) survival.
Results: 154 men were included in the study, of which 126 (82%) had %fPSA<15 and 28 (18%) had %fPSA≥15. Median follow up for %fPSA<15 and %fPSA≥15 was 75 and 69 months, respectively. Patients with %fPSA≥15 had increased hazard of receiving ADT (25% vs. 43%, adjusted HR 2.40 [95% CI 1.12-5.11]), developing metastatic disease (7.9% vs. 21%, adjusted HR 4.10 [95% CI 1.11-15.2]), and developing CRPC(4.0% vs. 14%, unadjusted HR 4.14 [95% CI 1.11-15.5]).
Conclusions: Patients with %fPSA≥15 were started on ADT earlier, and they progressed to CRPC and metastatic stage earlier. %fPSA of ≥15 in the setting of BCR after RP is an indicator of a more aggressive disease. Unlike in the diagnostic setting, a higher %fPSA portends a worse clinical outcome.