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Bone Scan Index: a prognostic imaging biomarker for high-risk prostate cancer patients receiving primary hormonal therapy

BACKGROUND: The objective of this study was to explore the prognostic value of the Bone Scan Index (BSI) obtained at the time of diagnosis in a group of high-risk prostate cancer patients receiving primary hormonal therapy. METHODS: This was a retrospective study based on 130 consecutive prostate ca...

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Autores principales: Kaboteh, Reza, Damber, Jan-Erik, Gjertsson, Peter, Höglund, Peter, Lomsky, Milan, Ohlsson, Mattias, Edenbrandt, Lars
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570487/
https://www.ncbi.nlm.nih.gov/pubmed/23384286
http://dx.doi.org/10.1186/2191-219X-3-9
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author Kaboteh, Reza
Damber, Jan-Erik
Gjertsson, Peter
Höglund, Peter
Lomsky, Milan
Ohlsson, Mattias
Edenbrandt, Lars
author_facet Kaboteh, Reza
Damber, Jan-Erik
Gjertsson, Peter
Höglund, Peter
Lomsky, Milan
Ohlsson, Mattias
Edenbrandt, Lars
author_sort Kaboteh, Reza
collection PubMed
description BACKGROUND: The objective of this study was to explore the prognostic value of the Bone Scan Index (BSI) obtained at the time of diagnosis in a group of high-risk prostate cancer patients receiving primary hormonal therapy. METHODS: This was a retrospective study based on 130 consecutive prostate cancer patients at high risk, based on clinical stage (T2c/T3/T4), Gleason score (8 to 10) and prostate-specific antigen (PSA) (> 20 ng/mL), who had undergone whole-body bone scans < 3 months after diagnosis and who received primary hormonal therapy. BSI was calculated using an automated method. Cox proportional-hazards regression models were used to investigate the association between clinical stage, Gleason score, PSA, BSI and survival. Discrimination between prognostic models was assessed using the concordance index (C-index). RESULTS: In a multivariate analysis, Gleason score (p = 0.01) and BSI (p < 0.001) were associated with survival, but clinical stage (p = 0.29) and PSA (p = 0.57) were not prognostic. The C-index increased from 0.66 to 0.71 when adding BSI to a model including clinical stage, Gleason score and PSA. The 5-year probability of survival was 55% for patients without metastases, 42% for patients with BSI < 1, 31% for patients with BSI = 1 to 5, and 0% for patients with BSI > 5. CONCLUSIONS: BSI can be used as a complement to PSA to risk-stratify high-risk prostate cancer patients at the time of diagnosis. This imaging biomarker, reflecting the extent of metastatic disease, can be of value both in clinical trials and in patient management when deciding on treatment.
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spelling pubmed-35704872013-02-13 Bone Scan Index: a prognostic imaging biomarker for high-risk prostate cancer patients receiving primary hormonal therapy Kaboteh, Reza Damber, Jan-Erik Gjertsson, Peter Höglund, Peter Lomsky, Milan Ohlsson, Mattias Edenbrandt, Lars EJNMMI Res Original Research BACKGROUND: The objective of this study was to explore the prognostic value of the Bone Scan Index (BSI) obtained at the time of diagnosis in a group of high-risk prostate cancer patients receiving primary hormonal therapy. METHODS: This was a retrospective study based on 130 consecutive prostate cancer patients at high risk, based on clinical stage (T2c/T3/T4), Gleason score (8 to 10) and prostate-specific antigen (PSA) (> 20 ng/mL), who had undergone whole-body bone scans < 3 months after diagnosis and who received primary hormonal therapy. BSI was calculated using an automated method. Cox proportional-hazards regression models were used to investigate the association between clinical stage, Gleason score, PSA, BSI and survival. Discrimination between prognostic models was assessed using the concordance index (C-index). RESULTS: In a multivariate analysis, Gleason score (p = 0.01) and BSI (p < 0.001) were associated with survival, but clinical stage (p = 0.29) and PSA (p = 0.57) were not prognostic. The C-index increased from 0.66 to 0.71 when adding BSI to a model including clinical stage, Gleason score and PSA. The 5-year probability of survival was 55% for patients without metastases, 42% for patients with BSI < 1, 31% for patients with BSI = 1 to 5, and 0% for patients with BSI > 5. CONCLUSIONS: BSI can be used as a complement to PSA to risk-stratify high-risk prostate cancer patients at the time of diagnosis. This imaging biomarker, reflecting the extent of metastatic disease, can be of value both in clinical trials and in patient management when deciding on treatment. Springer 2013-02-06 /pmc/articles/PMC3570487/ /pubmed/23384286 http://dx.doi.org/10.1186/2191-219X-3-9 Text en Copyright ©2013 Kaboteh et al.; licensee Springer. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Kaboteh, Reza
Damber, Jan-Erik
Gjertsson, Peter
Höglund, Peter
Lomsky, Milan
Ohlsson, Mattias
Edenbrandt, Lars
Bone Scan Index: a prognostic imaging biomarker for high-risk prostate cancer patients receiving primary hormonal therapy
title Bone Scan Index: a prognostic imaging biomarker for high-risk prostate cancer patients receiving primary hormonal therapy
title_full Bone Scan Index: a prognostic imaging biomarker for high-risk prostate cancer patients receiving primary hormonal therapy
title_fullStr Bone Scan Index: a prognostic imaging biomarker for high-risk prostate cancer patients receiving primary hormonal therapy
title_full_unstemmed Bone Scan Index: a prognostic imaging biomarker for high-risk prostate cancer patients receiving primary hormonal therapy
title_short Bone Scan Index: a prognostic imaging biomarker for high-risk prostate cancer patients receiving primary hormonal therapy
title_sort bone scan index: a prognostic imaging biomarker for high-risk prostate cancer patients receiving primary hormonal therapy
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3570487/
https://www.ncbi.nlm.nih.gov/pubmed/23384286
http://dx.doi.org/10.1186/2191-219X-3-9
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