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The significance of circulating tumor cells in prostate cancer patients undergoing adjuvant or salvage radiation therapy
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نویسنده
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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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منبع
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prostate cancer and prostatic diseases - 2015 - دوره : 18 - شماره : 4 - صفحه:358 -364
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چکیده
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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 ctcneg disease; p=0.032), and trended toward significance with the presence of seminal vesicle invasion (ctcpos; p=0.113) and extracapsular extension (ctcneg; 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.
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آدرس
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Western University, Department of Anatomy and Cell Biology, Canada. London Health Sciences Centre, London Regional Cancer Program, Canada, London Health Sciences Centre, London Regional Cancer Program, Canada. Western University, Department of Oncology, Canada, London Health Sciences Centre, London Regional Cancer Program, Canada. Western University, Department of Oncology, Canada, London Health Sciences Centre, London Regional Cancer Program, Canada. Western University, Department of Oncology, Canada, London Health Sciences Centre, London Regional Cancer Program, Canada. Western University, Department of Oncology, Canada, London Health Sciences Centre, London Regional Cancer Program, Canada. Western University, Department of Oncology, Canada, London Health Sciences Centre, London Regional Cancer Program, Canada. Western University, Department of Oncology, Canada, Western University, Department of Anatomy and Cell Biology, Department of Oncology, Canada. London Health Sciences Centre, London Regional Cancer Program, Canada, London Health Sciences Centre, London Regional Cancer Program, Canada. Western University, Department of Oncology, Canada
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Authors
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