Salvage Brachytherapy for Biochemically Recurrent Prostate Cancer following Primary Brachytherapy

Purpose. In this study, we evaluated our experience with salvage brachytherapy after discovery of biochemical recurrence after a prior brachytherapy procedure. Methods and Materials. From 2001 through 2012 twenty-one patients treated by brachytherapy within University of Kentucky or from outside cen...

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Main Authors: John M. Lacy, William A. Wilson, Raevti Bole, Li Chen, Ali S. Meigooni, Randall G. Rowland, William H. St. Clair
Format: Article
Language:English
Published: Wiley 2016-01-01
Series:Prostate Cancer
Online Access:http://dx.doi.org/10.1155/2016/9561494
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author John M. Lacy
William A. Wilson
Raevti Bole
Li Chen
Ali S. Meigooni
Randall G. Rowland
William H. St. Clair
author_facet John M. Lacy
William A. Wilson
Raevti Bole
Li Chen
Ali S. Meigooni
Randall G. Rowland
William H. St. Clair
author_sort John M. Lacy
collection DOAJ
description Purpose. In this study, we evaluated our experience with salvage brachytherapy after discovery of biochemical recurrence after a prior brachytherapy procedure. Methods and Materials. From 2001 through 2012 twenty-one patients treated by brachytherapy within University of Kentucky or from outside centers developed biochemical failure and had no evidence of metastases. Computed tomography (CT) scans were evaluated; patients who had an underseeded portion of their prostate were considered for reimplantation. Results. The majority of the patients in this study (61.9%) were low risk and median presalvage PSA was 3.49 (range 17.41–1.68). Mean follow-up was 61 months. At last follow-up after reseeding, 11/21 (52.4%) were free of biochemical recurrence. There was a trend towards decreased freedom from biochemical recurrence in low risk patients (p=0.12). International Prostate Symptom Scores (IPSS) increased at 3-month follow-up visits but decreased and were equivalent to baseline scores at 18 months. Conclusions. Salvage brachytherapy after primary brachytherapy is possible; however, in our experience the side-effect profile after the second brachytherapy procedure was higher than after the first brachytherapy procedure. In this cohort of patients we demonstrate that approximately 50% oncologic control, low risk patients appear to have better outcomes than others.
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publishDate 2016-01-01
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series Prostate Cancer
spelling doaj-art-4117ca72c4aa4cd19eec3685f1770f632025-08-20T02:07:52ZengWileyProstate Cancer2090-31112090-312X2016-01-01201610.1155/2016/95614949561494Salvage Brachytherapy for Biochemically Recurrent Prostate Cancer following Primary BrachytherapyJohn M. Lacy0William A. Wilson1Raevti Bole2Li Chen3Ali S. Meigooni4Randall G. Rowland5William H. St. Clair6Department of Urology, University of Kentucky College of Medicine, Lexington, KY 40536, USADepartment of Radiation Oncology, University of Kentucky College of Medicine, Lexington, KY 40536, USAUniversity of Kentucky College of Medicine, Lexington, KY 40536, USADepartment of Biostatistics, University of Kentucky College of Public Health, Lexington, KY 40536, USAComprehensive Cancer Centers of Nevada, Las Vegas, NV 89169, USADepartment of Urology, University of Kentucky College of Medicine, Lexington, KY 40536, USADepartment of Radiation Oncology, University of Kentucky College of Medicine, Lexington, KY 40536, USAPurpose. In this study, we evaluated our experience with salvage brachytherapy after discovery of biochemical recurrence after a prior brachytherapy procedure. Methods and Materials. From 2001 through 2012 twenty-one patients treated by brachytherapy within University of Kentucky or from outside centers developed biochemical failure and had no evidence of metastases. Computed tomography (CT) scans were evaluated; patients who had an underseeded portion of their prostate were considered for reimplantation. Results. The majority of the patients in this study (61.9%) were low risk and median presalvage PSA was 3.49 (range 17.41–1.68). Mean follow-up was 61 months. At last follow-up after reseeding, 11/21 (52.4%) were free of biochemical recurrence. There was a trend towards decreased freedom from biochemical recurrence in low risk patients (p=0.12). International Prostate Symptom Scores (IPSS) increased at 3-month follow-up visits but decreased and were equivalent to baseline scores at 18 months. Conclusions. Salvage brachytherapy after primary brachytherapy is possible; however, in our experience the side-effect profile after the second brachytherapy procedure was higher than after the first brachytherapy procedure. In this cohort of patients we demonstrate that approximately 50% oncologic control, low risk patients appear to have better outcomes than others.http://dx.doi.org/10.1155/2016/9561494
spellingShingle John M. Lacy
William A. Wilson
Raevti Bole
Li Chen
Ali S. Meigooni
Randall G. Rowland
William H. St. Clair
Salvage Brachytherapy for Biochemically Recurrent Prostate Cancer following Primary Brachytherapy
Prostate Cancer
title Salvage Brachytherapy for Biochemically Recurrent Prostate Cancer following Primary Brachytherapy
title_full Salvage Brachytherapy for Biochemically Recurrent Prostate Cancer following Primary Brachytherapy
title_fullStr Salvage Brachytherapy for Biochemically Recurrent Prostate Cancer following Primary Brachytherapy
title_full_unstemmed Salvage Brachytherapy for Biochemically Recurrent Prostate Cancer following Primary Brachytherapy
title_short Salvage Brachytherapy for Biochemically Recurrent Prostate Cancer following Primary Brachytherapy
title_sort salvage brachytherapy for biochemically recurrent prostate cancer following primary brachytherapy
url http://dx.doi.org/10.1155/2016/9561494
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