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...

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Veröffentlicht in:Prostate cancer and prostatic diseases 2015-12, Vol.18 (4), p.358-364
Hauptverfasser: Lowes, L E, Lock, M, Rodrigues, G, D’Souza, D, Bauman, G, Ahmad, B, Venkatesan, V, Allan, A L, Sexton, T
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container_end_page 364
container_issue 4
container_start_page 358
container_title Prostate cancer and prostatic diseases
container_volume 18
creator Lowes, L E
Lock, M
Rodrigues, G
D’Souza, D
Bauman, G
Ahmad, B
Venkatesan, V
Allan, A L
Sexton, T
description 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.
doi_str_mv 10.1038/pcan.2015.36
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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). 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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). 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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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>26238233</pmid><doi>10.1038/pcan.2015.36</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects 14/1
14/63
631/67/1059
631/67/589/466
692/308/575
692/53/2422
82/80
Biomarkers, Tumor
Biomedical and Life Sciences
Biomedicine
Cancer Research
Care and treatment
Cell Count
Complications and side effects
Follow-Up Studies
Health aspects
Humans
Male
Metastasis
Neoplasm Grading
Neoplasm Staging
Neoplastic Cells, Circulating - pathology
Original
original-article
Prostate cancer
Prostate-Specific Antigen - blood
Prostatic Neoplasms - mortality
Prostatic Neoplasms - pathology
Prostatic Neoplasms - radiotherapy
Radiotherapy
Radiotherapy, Adjuvant
Risk factors
Salvage Therapy
Survival Analysis
Treatment Outcome
title The significance of circulating tumor cells in prostate cancer patients undergoing adjuvant or salvage radiation therapy
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