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Normalization of prostate specific antigen in patients treated with intensity modulated radiotherapy for clinically localized prostate cancer

BACKGROUND: The purpose of this study was to determine the expected time to prostate specific antigen (PSA) normalization with or without neoadjuvant androgen deprivation (NAAD) therapy after treatment with intensity modulated radiotherapy (IMRT) for patients with clinically localized prostate cance...

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Autores principales: Schmitz, Matthew D, Padula, Gilbert DA, Chun, Patrick Y, Davis, Alan T
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949678/
https://www.ncbi.nlm.nih.gov/pubmed/20846422
http://dx.doi.org/10.1186/1748-717X-5-80
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author Schmitz, Matthew D
Padula, Gilbert DA
Chun, Patrick Y
Davis, Alan T
author_facet Schmitz, Matthew D
Padula, Gilbert DA
Chun, Patrick Y
Davis, Alan T
author_sort Schmitz, Matthew D
collection PubMed
description BACKGROUND: The purpose of this study was to determine the expected time to prostate specific antigen (PSA) normalization with or without neoadjuvant androgen deprivation (NAAD) therapy after treatment with intensity modulated radiotherapy (IMRT) for patients with clinically localized prostate cancer. METHODS: A retrospective cohort research design was used. A total of 133 patients with clinical stage T1c to T3b prostate cancer (2002 AJCC staging) treated in a community setting between January 2002 and July 2005 were reviewed for time to PSA normalization using 1 ng/mL and 2 ng/mL as criteria. All patients received IMRT as part of their management. Times to PSA normalization were calculated using the Kaplan-Meier method. Significance was assessed at p < 0.05. RESULTS: Fifty-six of the 133 patients received NAAD (42.1%). Thirty-one patients (23.8%) received radiation to a limited pelvic field followed by an IMRT boost, while 99 patients received IMRT alone (76.2%). The times to serum PSA normalization < 2 ng/mL when treated with or without NAAD were 298 ± 24 and 302 ± 33 days (mean ± SEM), respectively (p > 0.05), and 303 ± 24 and 405 ± 46 days, respectively, for PSA < 1 ng/mL (p < 0.05). Stage T1 and T2 tumors had significantly increased time to PSA normalization < 1 ng/mL in comparison to Stage T3 tumors. Also, higher Gleason scores were significantly correlated with a faster time to PSA normalization < 1 ng/mL. CONCLUSIONS: Use of NAAD in conjunction with IMRT leads to a significantly shortened time to normalization of serum PSA < 1 ng/mL in patients with clinically localized prostate cancer.
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spelling pubmed-29496782010-10-06 Normalization of prostate specific antigen in patients treated with intensity modulated radiotherapy for clinically localized prostate cancer Schmitz, Matthew D Padula, Gilbert DA Chun, Patrick Y Davis, Alan T Radiat Oncol Research BACKGROUND: The purpose of this study was to determine the expected time to prostate specific antigen (PSA) normalization with or without neoadjuvant androgen deprivation (NAAD) therapy after treatment with intensity modulated radiotherapy (IMRT) for patients with clinically localized prostate cancer. METHODS: A retrospective cohort research design was used. A total of 133 patients with clinical stage T1c to T3b prostate cancer (2002 AJCC staging) treated in a community setting between January 2002 and July 2005 were reviewed for time to PSA normalization using 1 ng/mL and 2 ng/mL as criteria. All patients received IMRT as part of their management. Times to PSA normalization were calculated using the Kaplan-Meier method. Significance was assessed at p < 0.05. RESULTS: Fifty-six of the 133 patients received NAAD (42.1%). Thirty-one patients (23.8%) received radiation to a limited pelvic field followed by an IMRT boost, while 99 patients received IMRT alone (76.2%). The times to serum PSA normalization < 2 ng/mL when treated with or without NAAD were 298 ± 24 and 302 ± 33 days (mean ± SEM), respectively (p > 0.05), and 303 ± 24 and 405 ± 46 days, respectively, for PSA < 1 ng/mL (p < 0.05). Stage T1 and T2 tumors had significantly increased time to PSA normalization < 1 ng/mL in comparison to Stage T3 tumors. Also, higher Gleason scores were significantly correlated with a faster time to PSA normalization < 1 ng/mL. CONCLUSIONS: Use of NAAD in conjunction with IMRT leads to a significantly shortened time to normalization of serum PSA < 1 ng/mL in patients with clinically localized prostate cancer. BioMed Central 2010-09-16 /pmc/articles/PMC2949678/ /pubmed/20846422 http://dx.doi.org/10.1186/1748-717X-5-80 Text en Copyright ©2010 Schmitz et al; licensee BioMed Central Ltd. 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 Research
Schmitz, Matthew D
Padula, Gilbert DA
Chun, Patrick Y
Davis, Alan T
Normalization of prostate specific antigen in patients treated with intensity modulated radiotherapy for clinically localized prostate cancer
title Normalization of prostate specific antigen in patients treated with intensity modulated radiotherapy for clinically localized prostate cancer
title_full Normalization of prostate specific antigen in patients treated with intensity modulated radiotherapy for clinically localized prostate cancer
title_fullStr Normalization of prostate specific antigen in patients treated with intensity modulated radiotherapy for clinically localized prostate cancer
title_full_unstemmed Normalization of prostate specific antigen in patients treated with intensity modulated radiotherapy for clinically localized prostate cancer
title_short Normalization of prostate specific antigen in patients treated with intensity modulated radiotherapy for clinically localized prostate cancer
title_sort normalization of prostate specific antigen in patients treated with intensity modulated radiotherapy for clinically localized prostate cancer
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2949678/
https://www.ncbi.nlm.nih.gov/pubmed/20846422
http://dx.doi.org/10.1186/1748-717X-5-80
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