The significance of circulating tumor cells in prostate cancer patients undergoing adjuvant or salvage radiation therapy
Background: Following radical prostatectomy, success of adjuvant and salvage radiation therapy (RT) is dependent on the absence of micrometastatic disease. However, reliable prognostic/predictive factors for determining this are lacking. Therefore, novel biomarkers are needed to assist with clinical...
Gespeichert in:
Veröffentlicht in: | Prostate cancer and prostatic diseases 2015-12, Vol.18 (4), p.358-364 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Background:
Following radical prostatectomy, success of adjuvant and salvage radiation therapy (RT) is dependent on the absence of micrometastatic disease. However, reliable prognostic/predictive factors for determining this are lacking. Therefore, novel biomarkers are needed to assist with clinical decision-making in this setting. Enumeration of circulating tumor cells (CTCs) using the regulatory-approved CellSearch System (CSS) is prognostic in metastatic prostate cancer. We hypothesize that CTCs may also be prognostic in the post-prostatectomy setting.
Methods:
Patient blood samples (
n
=55) were processed on the CSS to enumerate CTCs at 0, 6, 12 and 24 months after completion of RT. CTC values were correlated with predictive/prognostic factors and progression-free survival.
Results:
CTC status (presence/absence) correlated significantly with positive margins (increased likelihood of CTC
neg
disease;
P
=0.032), and trended toward significance with the presence of seminal vesicle invasion (CTC
pos
;
P
=0.113) and extracapsular extension (CTC
neg
;
P
=0.116). Although there was a trend toward a decreased time to biochemical failure (BCF) in baseline CTC-positive patients (
n
=9), this trend was not significant (hazard ratio (HR)=0.3505;
P
=0.166). However, CTC-positive status at any point (
n
=16) predicted for time to BCF (HR=0.2868;
P
=0.0437).
Conclusions:
One caveat of this study is the small sample size utilized (
n
=55) and the low number of patients with CTC-positive disease (
n
=16). However, our results suggest that CTCs may be indicative of disseminated disease and assessment of CTCs during RT may be helpful in clinical decision-making to determine, which patients may benefit from RT versus those who may benefit more from systemic treatments. |
---|---|
ISSN: | 1365-7852 1476-5608 |
DOI: | 10.1038/pcan.2015.36 |